Role of hospitalization for inflammatory bowel disease in the post-biologic era
Therapy for inflammatory bowel illness (IBD) typically requires specialised care. Whereas a lot of IBD care has shifted to the outpatient setting, hospitalizations stay a significant website of healthcare utilization and a large proportion of sufferers with inflammatory bowel illness require hospitalization or surgical procedure throughout their lifetime.
On this assessment, we strategy IBD care from the population-level with a particular give attention to hospitalization for IBD, together with the shifts from inpatient to outpatient care, the steadiness of emergency and elective hospitalizations, regionalization of specialty IBD care, and contribution of surgical procedure and endoscopy to hospitalized care.
Efficacy and Security of Twin Biologic Remedy in Sufferers With Inflammatory Bowel Illness: A Evaluation of the Literature
Utilizing 2 or extra remedy modalities to attain a synergistic impact in sufferers with refractory inflammatory bowel illness (IBD) has been an space of focus for a few years. This technique, referred to as mixture remedy, has been proposed for numerous therapeutic brokers, mostly biologics and immunomodulators.
Though the mainstay of biologic remedy for IBD has historically targeted on brokers focusing on tumor necrosis issue, the event of newer biologics with completely different targets, similar to vedolizumab and ustekinumab, has launched the opportunity of concomitant twin biologic remedy.
Twin biologic remedy has been proposed within the remedy algorithm for two kinds of sufferers with IBD: these with well-controlled luminal IBD and uncontrolled extraintestinal signs (secondary indications similar to arthritis or psoriasis) and people with refractory, uncontrolled IBD.
Up to now, the info on the efficacy and security of twin biologic remedy as a remedy for Crohn’s illness or ulcerative colitis stay fairly restricted. In actual fact, the overwhelming majority of the literature consists of case studies and case sequence. Given this paucity of high-level knowledge, physicians have appeared to bigger research on twin biologic remedy in different fields of medication, similar to rheumatology and dermatology.
The objective of this text is to summarize the present literature on using twin biologics in IBD, deal with the potential adversarial results or dangers related to mixture remedy, and spotlight future instructions in using this therapeutic modality.
Monitoring process-related impurities in biologics-host cell protein evaluation
Throughout biologics improvement, producers should reveal clearance of host cell impurities and contaminants to make sure drug purity, manufacturing course of consistency, and affected person security. Host cell proteins (HCPs) are a significant class of process-related impurities and require monitoring and documentation of their presence by means of improvement and manufacturing.
Even in residual quantities, they’re identified to have an effect on product high quality and efficacy in addition to affected person security. HCP evaluation utilizing enzyme-linked immunosorbent assay (HCP-ELISA) is the usual method, attributable to its easy dealing with, brief evaluation time, and excessive sensitivity for protein impurities.
Liquid chromatography mass spectrometry (LC-MS) is an orthogonal methodology for HCP evaluation and is more and more included in regulatory documentation. LC-MS presents benefits the place HCP-ELISA has drawbacks, e.g., the flexibility to determine and quantify particular person HCPs.
This text summarizes the obtainable data about monitoring HCPs in biologics and presents the latest tendencies in HCP evaluation with present state-of-the-art HCP measurement instruments. By means of case research, we current examples of HCP management methods which have been utilized in regulatory license purposes, utilizing an MS-based protection evaluation and HCP-ELISA and LC-MS for HCP quantification.
This offers novel perception into the speedy evolving technique of HCP evaluation. Enhancements in applied sciences to guage HCP-ELISA suitability and the implementation of orthogonal LC-MS strategies for HCP evaluation are necessary to rationally manipulate, engineer, and choose appropriate cell traces and downstream processing steps to restrict problematic HCPs.
Residual Ache within the Context of Choosing and Switching Biologic Remedy in Inflammatory Rheumatic Ailments
For a few years, inflammatory rheumatic ailments (IRDs) represented a supply of disappointment in medical care attributable to the mediocre efficacy of the obtainable therapies. A few of these ailments, like Rheumatoid Arthritis (RA) or Ankylosing Spondylitis (AS), precipitated concern within the normal inhabitants, particularly attributable to related joint deformities and subsequent disabilities.
Nevertheless, within the final 20 years, a brand new profitable class of antirheumatic medication has change into obtainable: biologic Illness-Modifying Antirheumatic Medication (bDMARDs). As a consequence of this revolutionary remedy, the times are over when joint and backbone deformities outlined the situation of an individual with RA or AS. Nonetheless, expectations are larger in the present day, and different scientific issues, (not solely solved by bDMARDs), appear to drive the drug choice through the span of rheumatic ailments.
Most of those points are lined by the time period “unmet wants.” One of the vital intriguing of such wants is the residual ache (RP) in sufferers which are in any other case within the organic remission of the illness. Current in a big proportion of the sufferers that enter remission standing, RP is poorly understood and managed. In recent times, new knowledge has change into obtainable on this space and new conceptual clarifications have occurred.
On this assessment, we clarify the varied nature of RP and the need of remedy diversification in such conditions. All in all, we imagine this situation is way extra complicated than easy ache and consists of different scientific facets, too (like fatigue or temper modifications) so the phrases Submit-Remission Syndrome (PRS), and PRS ache may be extra acceptable.
Immune Test Level Inhibitors in Major Cutaneous T-Cell Lymphomas: Biologic Rationale, Medical Outcomes and Future Views
Major cutaneous T-cell lymphomas (PCTCL) are the most typical kinds of cutaneous lymphomas, with Mycosis fungoides as essentially the most frequent subtype. Apart from early phases which normally have a superb prognosis, superior phases stay a terrific therapeutic problem with low survival charges.
Up to now, not one of the at present obtainable therapeutic choices have considerably improved the outcomes of superior cutaneous lymphomas. Latest research have demonstrated that immune-checkpoint molecules, similar to PD-1 and CTLA-4, play half within the proliferation pathways of neoplastic T-cells, in addition to in different tumors.
Radius™ 24-Well Cell Migration Assay |
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| CBA-125 | Cell Biolabs | 24 assays | EUR 356 |
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Description: Excepted Quantities |
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Radius™ 24-Well Cell Migration Assay |
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| CBA-125-5 | Cell Biolabs | 5 x 24 assays | EUR 1516 |
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Description: Excepted Quantities |
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Radius™ 96-Well Cell Migration Assay |
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| CBA-126 | Cell Biolabs | 96 assays | EUR 416 |
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Description: Excepted Quantities |
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Radius™ 96-Well Cell Migration Assay |
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| CBA-126-5 | Cell Biolabs | 5 x 96 assays | EUR 1788 |
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Description: Excepted Quantities |
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Radius™ 48-Well Cell Migration Assay |
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| CBA-5037 | Cell Biolabs | 48 assays | EUR 372 |
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Description: Excepted Quantities |
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Radius™ 48-Well Cell Migration Assay |
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| CBA-5037-5 | Cell Biolabs | 5 x 48 assays | EUR 1592 |
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Description: Excepted Quantities |
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Radius 24-Well Cell Migration Assay, (Laminin Coated) |
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| CBA-125-LN | Cell Biolabs | 24 assays | EUR 714 |
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Description: The Radius Cell Migration Assay provides a unique alternative to conventional cell migration assays using the Boyden chamber. Unlike Boyden chamber assays which may only be analyzed at endpoint, the Radius assay uses a proprietary cell culture plate containing a carefully-defined biocompatible hydrogel (Radius gel) spot centralized at the bottom of each well. When cells are seeded in the well, they will attach everywhere except on the Radius gel, creating a cell-free zone. Following cell seeding the Radius gel is removed, allowing migratory cells to move across the area and close the gap. |
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Radius 24-Well Cell Migration Assay, (Fibronectin Coated) |
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| CBA-125-FN | Cell Biolabs | 24 assays | EUR 714 |
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Description: The Radius Cell Migration Assay provides a unique alternative to conventional cell migration assays using the Boyden chamber. Unlike Boyden chamber assays which may only be analyzed at endpoint, the Radius assay uses a proprietary cell culture plate containing a carefully-defined biocompatible hydrogel (Radius gel) spot centralized at the bottom of each well. When cells are seeded in the well, they will attach everywhere except on the Radius gel, creating a cell-free zone. Following cell seeding the Radius gel is removed, allowing migratory cells to move across the area and close the gap. |
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Radius 24-Well Cell Migration Assay, (ECM Array Coated) |
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| CBA-125-ECM | Cell Biolabs | 24 wells | EUR 838.8 |
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Description: The Radius Cell Migration Assay provides a unique alternative to conventional cell migration assays using the Boyden chamber. Unlike Boyden chamber assays which may only be analyzed at endpoint, the Radius assay uses a proprietary cell culture plate containing a carefully-defined biocompatible hydrogel (Radius gel) spot centralized at the bottom of each well. When cells are seeded in the well, they will attach everywhere except on the Radius gel, creating a cell-free zone. Following cell seeding the Radius gel is removed, allowing migratory cells to move across the area and close the gap. |
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Radius 24-Well Cell Migration Assay, (Collagen I Coated) |
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| MBS168926-24Assays | MyBiosource | 24Assays | EUR 705 |
Radius 24-Well Cell Migration Assay, (Collagen I Coated) |
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| MBS168926-5x24Assays | MyBiosource | 5x24Assays | EUR 3250 |
Radius™ 24-Well Cell Migration Assay, (Collagen I Coated) |
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| CBA-125-COL | Cell Biolabs | 24 assays | EUR 520 |
RAD16-I |
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| 4033805.2001 | Bachem | 0.5 mg | EUR 230.37 |
RAD16-I |
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| 4033805.2002 | Bachem | 1 mg | EUR 806.72 |
Radil (untagged ORF) - Rat Rap GTPase interactor (Radil), (10 ug) |
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| RN213686 | Origene Technologies GmbH | 10 µg | Ask for price |
RAD51-IN-3 |
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| HY-136604 | MedChemExpress | 10 mg | EUR 4329.07 |
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Description: RAD51-IN-3 is a Rad51 inhibitor extracted from patent WO2019051465A1, compound Example 66A[1]. |
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RAD51-IN-8 |
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| HY-150958 | MedChemExpress | Get quote | Ask for price |
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Description: RAD51-IN-8, a new RAD51 binder, is a RAD51-BRCA2 inhibitor that inhibits the RAD51 BRCA2 protein protein interaction. RAD51-IN-8 also is a protein−protein interaction (PPI) inhibitor. RAD51-IN-8 has inhibitory activity for H4A4 with an EC50 value of 19 μM[1]. |
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RAD51-IN-1 |
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| HY-122705 | MedChemExpress | 10 mg | EUR 389.62 |
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Description: RAD51-IN-1, a derivative of B02, is a potent inhibitor of RAD51. RAD51-IN-1 can be used for cancer research[1]. |
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RAD51-IN-4 |
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| HY-143735 | MedChemExpress | Get quote | Ask for price |
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Description: RAD51-IN-4 is a potent inhibitor of RAD51. RAD51 is a eukaryote gene. RAD51-IN-4 has the potential for the research of conditions involving mitochondrial defects (extracted from patent WO2019014315A1, compound R12)[1]. |
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RAD51-IN-5 |
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| HY-143736 | MedChemExpress | 10 mg | EUR 4166.73 |
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Description: RAD51-IN-5 is a potent inhibitor of RAD51. RAD51 is a eukaryote gene. RAD51-IN-5 has the potential for the research of conditions involving mitochondrial defects (extracted from patent WO2021164746A1, compound 3)[1]. |
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RAD51-IN-6 |
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| HY-143737 | MedChemExpress | Get quote | Ask for price |
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Description: RAD51-IN-6 is a potent inhibitor of RAD51. RAD51 is a eukaryote gene. RAD51-IN-6 has the potential for the research of conditions involving mitochondrial defects (extracted from patent WO2021164746A1, compound 23)[1]. |
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RAD51-IN-7 |
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| HY-143741 | MedChemExpress | Get quote | Ask for price |
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Description: RAD51-IN-7 is a potent inhibitor of RAD51. RAD51 is a eukaryote gene. RAD51-IN-7 has the potential for the research of conditions involving mitochondrial defects (extracted from patent WO2021164746A1, compound 71)[1]. |
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RAD51-IN-2 |
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| MBS3844025-10mg | MyBiosource | 10mg | EUR 1905 |
RAD51-IN-2 |
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| MBS3844025-1mg | MyBiosource | 1mg | EUR 430 |
RAD51-IN-2 |
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| MBS3844025-5mg | MyBiosource | 5mg | EUR 1165 |
RAD51-IN-2 |
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| MBS3844025-5x10mg | MyBiosource | 5x10mg | EUR 8565 |
RAD51-IN-2 |
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| MBS5767467-10mg | MyBiosource | 10mg | EUR 965 |
RAD51-IN-2 |
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| MBS5767467-25mg | MyBiosource | 25mg | EUR 1905 |
RAD51-IN-2 |
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| MBS5767467-5x25mg | MyBiosource | 5x25mg | EUR 8430 |
RAD51-IN-3 |
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| MBS5800225-5mg | MyBiosource | 5(mg | EUR 915 |
RAD51-IN-3 |
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| MBS5800225-5x5mg | MyBiosource | 5x5(mg | EUR 3970 |
RAD51-IN-7 |
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| T63728-10mg | TargetMol Chemicals | 10mg | Ask for price |
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Description: RAD51-IN-7 |
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RAD51-IN-7 |
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| T63728-1g | TargetMol Chemicals | 1g | Ask for price |
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Description: RAD51-IN-7 |
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RAD51-IN-7 |
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| T63728-1mg | TargetMol Chemicals | 1mg | Ask for price |
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Description: RAD51-IN-7 |
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RAD51-IN-7 |
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| T63728-50mg | TargetMol Chemicals | 50mg | Ask for price |
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Description: RAD51-IN-7 |
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RAD51-IN-7 |
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| T63728-5mg | TargetMol Chemicals | 5mg | Ask for price |
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Description: RAD51-IN-7 |
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RAD51-IN-6 |
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| T63883-10mg | TargetMol Chemicals | 10mg | Ask for price |
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Description: RAD51-IN-6 |
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RAD51-IN-6 |
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| T63883-1g | TargetMol Chemicals | 1g | Ask for price |
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Description: RAD51-IN-6 |
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RAD51-IN-6 |
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| T63883-1mg | TargetMol Chemicals | 1mg | Ask for price |
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Description: RAD51-IN-6 |
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RAD51-IN-6 |
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| T63883-50mg | TargetMol Chemicals | 50mg | Ask for price |
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Description: RAD51-IN-6 |
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RAD51-IN-6 |
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| T63883-5mg | TargetMol Chemicals | 5mg | Ask for price |
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Description: RAD51-IN-6 |
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RAD51-IN-5 |
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| T63892-10mg | TargetMol Chemicals | 10mg | Ask for price |
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Description: RAD51-IN-5 |
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RAD51-IN-5 |
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| T63892-1g | TargetMol Chemicals | 1g | Ask for price |
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Description: RAD51-IN-5 |
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RAD51-IN-5 |
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| T63892-1mg | TargetMol Chemicals | 1mg | Ask for price |
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Description: RAD51-IN-5 |
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RAD51-IN-5 |
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| T63892-50mg | TargetMol Chemicals | 50mg | Ask for price |
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Description: RAD51-IN-5 |
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RAD51-IN-5 |
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| T63892-5mg | TargetMol Chemicals | 5mg | Ask for price |
|
Description: RAD51-IN-5 |
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RAD51-IN-2 |
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| T12682-10mg | TargetMol Chemicals | 10mg | Ask for price |
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Description: RAD51-IN-2 |
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RAD51-IN-2 |
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| T12682-1g | TargetMol Chemicals | 1g | Ask for price |
|
Description: RAD51-IN-2 |
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RAD51-IN-2 |
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| T12682-1mg | TargetMol Chemicals | 1mg | Ask for price |
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Description: RAD51-IN-2 |
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RAD51-IN-2 |
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| T12682-50mg | TargetMol Chemicals | 50mg | Ask for price |
|
Description: RAD51-IN-2 |
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RAD51-IN-2 |
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| T12682-5mg | TargetMol Chemicals | 5mg | Ask for price |
|
Description: RAD51-IN-2 |
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RAD51-IN-3 |
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| T39824-10mg | TargetMol Chemicals | 10mg | Ask for price |
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Description: RAD51-IN-3 |
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RAD51-IN-3 |
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| T39824-1g | TargetMol Chemicals | 1g | Ask for price |
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Description: RAD51-IN-3 |
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RAD51-IN-3 |
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| T39824-1mg | TargetMol Chemicals | 1mg | Ask for price |
|
Description: RAD51-IN-3 |
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RAD51-IN-3 |
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| T39824-50mg | TargetMol Chemicals | 50mg | Ask for price |
|
Description: RAD51-IN-3 |
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RAD51-IN-3 |
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| T39824-5mg | TargetMol Chemicals | 5mg | Ask for price |
|
Description: RAD51-IN-3 |
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RAD51-IN-8 |
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| T61469-10mg | TargetMol Chemicals | 10mg | Ask for price |
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Description: RAD51-IN-8 |
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RAD51-IN-8 |
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| T61469-1g | TargetMol Chemicals | 1g | Ask for price |
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Description: RAD51-IN-8 |
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RAD51-IN-8 |
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| T61469-1mg | TargetMol Chemicals | 1mg | Ask for price |
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Description: RAD51-IN-8 |
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RAD51-IN-8 |
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| T61469-50mg | TargetMol Chemicals | 50mg | Ask for price |
|
Description: RAD51-IN-8 |
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RAD51-IN-8 |
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| T61469-5mg | TargetMol Chemicals | 5mg | Ask for price |
|
Description: RAD51-IN-8 |
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RAD51-IN-1 |
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| T9271-10mg | TargetMol Chemicals | 10mg | Ask for price |
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Description: RAD51-IN-1 |
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RAD51-IN-1 |
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| T9271-1g | TargetMol Chemicals | 1g | Ask for price |
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Description: RAD51-IN-1 |
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RAD51-IN-1 |
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| T9271-1mg | TargetMol Chemicals | 1mg | Ask for price |
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Description: RAD51-IN-1 |
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RAD51-IN-1 |
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| T9271-50mg | TargetMol Chemicals | 50mg | Ask for price |
|
Description: RAD51-IN-1 |
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RAD51-IN-1 |
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| T9271-5mg | TargetMol Chemicals | 5mg | Ask for price |
|
Description: RAD51-IN-1 |
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Rabbit Polyclonal antibody to Radixin (radixin) |
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| TA308208 | Origene Technologies GmbH | 100 µl | Ask for price |
Recombinant Vigna radiata var. radiata Albumin-1 (LEG) |
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| MBS7101245-002mgBaculovirus | MyBiosource | 0.02mg(Baculovirus) | EUR 965 |
Recombinant Vigna radiata var. radiata Albumin-1 (LEG) |
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| MBS7101245-002mgEColi | MyBiosource | 0.02mg(E-Coli) | EUR 520 |
Recombinant Vigna radiata var. radiata Albumin-1 (LEG) |
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| MBS7101245-002mgYeast | MyBiosource | 0.02mg(Yeast) | EUR 715 |
Recombinant Vigna radiata var. radiata Albumin-1 (LEG) |
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| MBS7101245-01mgEColi | MyBiosource | 0.1mg(E-Coli) | EUR 615 |
Recombinant Vigna radiata var. radiata Albumin-1 (LEG) |
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| MBS7101245-01mgYeast | MyBiosource | 0.1mg(Yeast) | EUR 835 |
RAD5-IN-1 |
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| MBS5765714-10mg | MyBiosource | 10mg | EUR 180 |
RAD5-IN-1 |
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| MBS5765714-25mg | MyBiosource | 25mg | EUR 255 |
RAD5-IN-1 |
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| MBS5765714-2mg | MyBiosource | 2mg | EUR 145 |
RAD5-IN-1 |
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| MBS5765714-50mg | MyBiosource | 50mg | EUR 350 |
RAD5-IN-1 |
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| MBS5765714-5mg | MyBiosource | 5mg | EUR 150 |
Recombinant Vigna radiata var. radiata Cytochrome c |
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| MBS1214063-002mgBaculovirus | MyBiosource | 0.02mg(Baculovirus) | EUR 1035 |
Recombinant Vigna radiata var. radiata Cytochrome c |
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| MBS1214063-002mgEColi | MyBiosource | 0.02mg(E-Coli) | EUR 610 |
Recombinant Vigna radiata var. radiata Cytochrome c |
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| MBS1214063-002mgYeast | MyBiosource | 0.02mg(Yeast) | EUR 785 |
Recombinant Vigna radiata var. radiata Cytochrome c |
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| MBS1214063-01mgEColi | MyBiosource | 0.1mg(E-Coli) | EUR 710 |
Recombinant Vigna radiata var. radiata Cytochrome c |
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| MBS1214063-01mgYeast | MyBiosource | 0.1mg(Yeast) | EUR 920 |
Radil (Myc-DDK-tagged ORF) - Rat Rap GTPase interactor (Radil), (10 ug) |
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| RR213686 | Origene Technologies GmbH | 10 µg | Ask for price |
RADIL (untagged)-Human Ras association and DIL domains (RADIL) |
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| SC304558 | Origene Technologies GmbH | 10 µg | Ask for price |
RADIL (GFP-tagged) - Human Ras association and DIL domains (RADIL) |
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| RG222590 | Origene Technologies GmbH | 10 µg | Ask for price |
Radil (untagged) - Mouse Ras association and DIL domains (Radil), (10ug) |
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| MC203521 | Origene Technologies GmbH | 10 µg | Ask for price |
RADIL |
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| CSB-CL853440HU1 | Cusabio | 10 μg plasmid + 200μl Glycerol | Ask for price |
RADIL |
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| CSB-CL853440HU2 | Cusabio | 10 μg plasmid + 200μl Glycerol | Ask for price |
Radil (Myc-DDK-tagged) - Mouse Ras association and DIL domains (Radil) |
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| MR211583 | Origene Technologies GmbH | 10 µg | Ask for price |
Lenti ORF clone of Radil (mGFP-tagged ORF) - Rat Rap GTPase interactor (Radil), (10 ug) |
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| RR213686L4 | Origene Technologies GmbH | 10 µg | Ask for price |
RADIL (Myc-DDK-tagged)-Human Ras association and DIL domains (RADIL) |
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| RC222590 | Origene Technologies GmbH | 10 µg | Ask for price |
Lenti ORF clone of Radil (Myc-DDK-tagged ORF) - Rat Rap GTPase interactor (Radil), (10 ug) |
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| RR213686L3 | Origene Technologies GmbH | 10 µg | Ask for price |
Radixin |
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| AP86892 | SAB | 1mg | EUR 2640 |
Radixin |
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| AP86897 | SAB | 1mg | EUR 2640 |
Radixin |
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| AP87237 | SAB | 1mg | EUR 2640 |
Radixin |
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| AP87300 | SAB | 1mg | EUR 2640 |
Radixin |
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| AP87357 | SAB | 1mg | EUR 2640 |
Radixin |
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| E8ET1610-41 | EnoGene | 100ul | EUR 275 |
|
Description: Available in various conjugation types. |
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Radixin |
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| MBS8533955-01mL | MyBiosource | 0.1mL | EUR 345 |
Radixin |
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| MBS8533955-01mLAF405L | MyBiosource | 0.1mL(AF405L) | EUR 565 |
Radixin |
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| MBS8533955-01mLAF405S | MyBiosource | 0.1mL(AF405S) | EUR 565 |
Radixin |
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| MBS8533955-01mLAF610 | MyBiosource | 0.1mL(AF610) | EUR 565 |
Radixin |
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| MBS8533955-01mLAF635 | MyBiosource | 0.1mL(AF635) | EUR 565 |
Lenti ORF clone of Radil (mGFP-tagged) - Mouse Ras association and DIL domains (Radil) |
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| MR211583L4 | Origene Technologies GmbH | 10 µg | Ask for price |
Lenti ORF particles, Radil (GFP-tagged ORF) - Rat Rap GTPase interactor (Radil), 200ul, >10^7 TU/mL |
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| RR213686L4V | Origene Technologies GmbH | 200 µl | Ask for price |
RDX, ID (Radixin) |
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| MBS6009424-005mg | MyBiosource | 0.05(mg | EUR 745 |
RDX, ID (Radixin) |
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| MBS6009424-5x005mg | MyBiosource | 5x0.05mg | EUR 3195 |
Radish cDNA |
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| PLD-1083 | Zyagen | 30 reactions | EUR 498 |
RAD16-I hydrochloride |
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| MBS5799991-25mg | MyBiosource | 25(mg | EUR 1030 |
RAD16-I hydrochloride |
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| MBS5799991-5x25mg | MyBiosource | 5x25(mg | EUR 4490 |
RAD16-I hydrochloride |
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| T39531-10mg | TargetMol Chemicals | 10mg | Ask for price |
|
Description: RAD16-I hydrochloride |
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RAD16-I hydrochloride |
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| T39531-1g | TargetMol Chemicals | 1g | Ask for price |
|
Description: RAD16-I hydrochloride |
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RAD16-I hydrochloride |
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| T39531-1mg | TargetMol Chemicals | 1mg | Ask for price |
|
Description: RAD16-I hydrochloride |
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RAD16-I hydrochloride |
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| T39531-50mg | TargetMol Chemicals | 50mg | Ask for price |
|
Description: RAD16-I hydrochloride |
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RAD16-I hydrochloride |
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| T39531-5mg | TargetMol Chemicals | 5mg | Ask for price |
|
Description: RAD16-I hydrochloride |
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Recombinant Vigna radiata var. radiata Auxin-induced protein 22D (AUX22D) |
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| MBS1159245-002mgBaculovirus | MyBiosource | 0.02mg(Baculovirus) | EUR 1110 |
Recombinant Vigna radiata var. radiata Auxin-induced protein 22D (AUX22D) |
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| MBS1159245-002mgEColi | MyBiosource | 0.02mg(E-Coli) | EUR 695 |
Recombinant Vigna radiata var. radiata Auxin-induced protein 22D (AUX22D) |
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| MBS1159245-002mgYeast | MyBiosource | 0.02mg(Yeast) | EUR 865 |
Recombinant Vigna radiata var. radiata Auxin-induced protein 22D (AUX22D) |
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| MBS1159245-01mgEColi | MyBiosource | 0.1mg(E-Coli) | EUR 830 |
Recombinant Vigna radiata var. radiata Auxin-induced protein 22D (AUX22D) |
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| MBS1159245-01mgYeast | MyBiosource | 0.1mg(Yeast) | EUR 1015 |
Recombinant Vigna radiata var. radiata Auxin-induced protein 22A (AUX22A) |
|||
| MBS1145153-002mgBaculovirus | MyBiosource | 0.02mg(Baculovirus) | EUR 1115 |
Recombinant Vigna radiata var. radiata Auxin-induced protein 22A (AUX22A) |
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| MBS1145153-002mgEColi | MyBiosource | 0.02mg(E-Coli) | EUR 695 |
Therefore, the potential function of immune-checkpoint-inhibitors in treating cutaneous lymphomas has been investigated within the final years. Herein, we define the present data concerning the function of immune-checkpoint molecules in PCTCL, their signaling pathways, microenvironment and therapeutic inhibition rationale. Furthermore, we assessment the printed knowledge on immunotherapies in PCTCL and summarize the at present ongoing scientific trials on this subject.
