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Mouse Monoclonal GKLF antibody [1E5] (STJ98109)
Supplier: St John’s Laboratory Ltd.
Recommended applications: WB, IHC, ELISA
Recommended dilution: WB 1:500-1:2000; IHC 1:200-1:1000; ELISA 1:10000
Recommended protocols: check protocols
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Check alternative names for the antibodyExpand
MS4A1 antibody, CD20 antibody,|APY antibody|ATOPY antibody|Fc epsilon receptor I beta-chain antibody|Fc IgE receptor beta chain antibody|FCER1B antibody|FCERB_HUMAN antibody|FcERI antibody|High affinity immunoglobulin epsilon receptor subunit beta antibody|IgE Fc receptor subunit beta antibody|IGEL antibody|IGHER antibody|Membrane-spanning 4-domains subfamily A member 2 antibody|MS4A1 antibody|Ms4a2 antibody|Anti-CD20 antibody [EP459Y] (ab78237)
SCBT cat No: sc-70582|sc-58982|sc-58983|sc-19990|sc-7733|sc-393894|sc-15361|sc-7736|sc-58985|sc-51531|
GKLF Monoclonal Antibody
|Catalogue No.|| |
GKLF Monoclonal Antibody detects endogenous levels of GKLF protein.
Purified recombinant fragment of human GKLF expressed in E Coli
WB, IHC, ELISA
|Recommended dilution|| |
WB 1:500-1:2000; IHC 1:200-1:1000; ELISA 1:10000
GKLF Antibody was tube-contained. Ascitic fluid containing 0.03% sodium azide.
GKLF Antibody was purified using affinity purification.
-20 Celsius degree. Avoid repeated freeze/thaw cycles.
|Alternative antibody names|| |
B-lymphocyte antigen CD20 antibody, B-lymphocyte surface antigen B1 antibody, Bp35 antibody, Leukocyte surface antigen Leu-16 antibody, Membrane-spanning 4-domains subfamily A member 1 antibody, CD antigen CD20 antibody
|Protein names|| |
B-lymphocyte antigen CD20 , B-lymphocyte surface antigen B1 , Bp35 , Leukocyte surface antigen Leu-16 , Membrane-spanning 4-domains subfamily A member 1 , CD antigen CD20
|Protein function|| |
This protein may be involved in the regulation of B-cell activation and proliferation.
|Protein tissue specificity|| |
Expressed on B-cells.
|Involvement in disease|| |
Immunodeficiency, common variable, 5 (CVID5) [MIM:613495]: A primary immunodeficiency characterized by antibody deficiency, hypogammaglobulinemia, recurrent bacterial infections and an inability to mount an antibody response to antigen. The defect results from a failure of B-cell differentiation and impaired secretion of immunoglobulins; the numbers of circulating B-cells is usually in the normal range, but can be low. . Note: The disease is caused by mutations affecting the gene represented in this entry.
|Protein sequence and domain|| |
Belongs to the MS4A family.
|Protein post-translational modifications|| |
Phosphorylated. Might be functionally regulated by protein kinase(s).
|Protein cellular localization|| |
Cell membrane / Multi-pass membrane protein / Cell membrane / Lipid-anchor
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St John’s Laboratory Ltd.
|Product type|| |
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