Anti-Braf(V600E) Mouse Monoclonal Antibody

价格:¥3800.00
品牌:NEWLF   
货号:NL25080
规格:100ul

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  • 概述

     

     

    Product  Description

     

       Description     Anti-Braf (V600E) Mouse Monoclonal Antibody
       Another Name     Anti-Braf (Mutated  V600E) Mouse Monoclonal Antibody
       Catalog Number     NL25080
       Size:      100 µl
       Tested Applications:       ELISA  WB  IF  IHC             ELISA:1:500-1:1000       WB:1:500-1:1000     IF:1:100-1:200      IHC:1:50-1:200
       Cited  Applications:     WB  IF  IHC
       Tested Reactivity:      Human , mouse   Rat
       Cited  Reactivity:        Human , mouse   Rat
       Gene Symbol:       NS7; B-raf; BRAF1; RAFB1; B-RAF1
       Immunogen :       A synthetic peptide from the internal region of human BRAF which includes the mutation of V600E
       Concentration:                 1mg/ml
       Host/Isotype:                      mouse/IgG2b
       Class:                    monnoclonal
       Type:                                   Antibody
       Predicted mv:                      84KDa
       Observed mv:                  84KDa
       Uniprot:                               p15056
       Constituents:       PBS (without Mg2+ and Ca2+), pH 7.4, 150 mM NaCl, 50% glycerol
       Storage Conditions:        Store at -20°C for one year after shipment

      

        Background:  

        This gene encodes a protein belonging to the RAF family of serine/threonine protein kinases. This protein plays a

        role in regulating the MAP kinase/ERK signaling pathway, which affects cell division, differentiation, and secretion. 

        Mutations in this gene, most commonly the V600E mutation, are the most frequently identified cancer-causing 

        mutations in melanoma, and have been identified in various other cancers as well, including non-Hodgkin lymphoma,

        colorectal cancer, thyroid carcinoma, non-small cell lung carcinoma, hairy cell leukemia and adenocarcinoma of lung.

        Mutations in this gene are also associated with cardiofaciocutaneous, Noonan, and Costello syndromes, which exhibit 

        overlapping phenotypes. A pseudogene of this gene has been identified on the X chromosome.

     


     

     

     

    Tested Applications:  WB

     

     

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    Tested Applications:  IF

     

        

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    Tested Applications: IHC

     

     

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