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Mouse Monoclonal CD19 antibody [2E2] (STJ97911)
Supplier: St John’s Laboratory Ltd.
Recommended applications: IF, FC, ELISA
Recommended dilution: IF 1:200-1:1000; FC 1:200-1:400; ELISA 1:10000
Recommended protocols: check protocols
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Check alternative names for the antibodyExpand
CD19 antibody,|Antibody deficiency due to defect in CD19, included antibody|AW495831 antibody|B lymphocyte antigen CD19 antibody|B lymphocyte surface antigen B4 antibody|B-lymphocyte antigen CD19 antibody|B-lymphocyte surface antigen B4 antibody|B4 antibody|CD19 antibody|CD19 antigen antibody|CD19 molecule antibody|Cd19 protein antibody|CD19_HUMAN antibody|CVID3 antibody|Differentiation antigen CD19 antibody|Leu 12 antibody|Leu-12 antibody|Leu12 antibody|MGC109570 antibody|MGC12802 antibody|T-cell surface antigen Leu-12 antibody|Anti-CD19 antibody [2E2B6B10] (ab31947)
SCBT cat No: sc-390244|sc-69736|sc-8498|sc-373897|sc-20922|sc-18884|sc-18894|sc-19650|sc-69735|sc-51529|sc-8500|sc-53191|sc-8499|
CD19 Monoclonal Antibody
|Catalogue No.|| |
CD19 Monoclonal Antibody detects endogenous levels of CD19 protein.
Purified recombinant fragment of human CD19 expressed in E Coli
IF, FC, ELISA
|Recommended dilution|| |
IF 1:200-1:1000; FC 1:200-1:400; ELISA 1:10000
CD19 Antibody was tube-contained. Ascitic fluid containing 0.03% sodium azide.
CD19 Antibody was purified using affinity purification.
-20 Celsius degree. Avoid repeated freeze/thaw cycles.
|Alternative antibody names|| |
B-lymphocyte antigen CD19 antibody, B-lymphocyte surface antigen B4 antibody, Differentiation antigen CD19 antibody, T-cell surface antigen Leu-12 antibody, CD antigen CD19 antibody
|Protein names|| |
B-lymphocyte antigen CD19 , B-lymphocyte surface antigen B4 , Differentiation antigen CD19 , T-cell surface antigen Leu-12 , CD antigen CD19
|Protein function|| |
Assembles with the antigen receptor of B-lymphocytes in order to decrease the threshold for antigen receptor-dependent stimulation.
|Involvement in disease|| |
Immunodeficiency, common variable, 3 (CVID3) [MIM:613493]: 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|| |
Contains 2 Ig-like C2-type (immunoglobulin-like) domains.
|Protein post-translational modifications|| |
Phosphorylated on serine and threonine upon DNA damage, probably by ATM or ATR. Phosphorylated on tyrosine following B-cell activation. Phosphorylated on tyrosine residues by LYN.
|Protein cellular localization|| |
Membrane; Single-pass type I membrane protein
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St John’s Laboratory Ltd.
|Product type|| |
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