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Mouse Monoclonal CD3E antibody [4E2] (STJ97925)
Supplier: St John’s Laboratory Ltd.
Recommended applications: WB, FC, ELISA
Recommended dilution: WB 1:500-1:2000; FC 1:200-1:400; ELISA 1:10000
Recommended protocols: check protocols
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Check alternative names for the antibodyExpand
CD3E antibody, T3E antibody,|CD3 epsilon antibody|CD3e antibody|CD3e antigen epsilon polypeptide (TiT3 complex) antibody|CD3E antigen epsilon polypeptide antibody|CD3E antigen, epsilon subunit antibody|CD3e molecule epsilon antibody|CD3e molecule, epsilon (CD3 TCR complex) antibody|CD3e molecule, epsilon (CD3-TCR complex) antibody|CD3E_HUMAN antibody|IMD18 antibody|T cell antigen receptor complex epsilon subunit of T3 antibody|T cell surface antigen T3/Leu 4 epsilon chain antibody|T cell surface glycoprotein CD3 epsilon chain antibody|T-cell surface antigen T3/Leu-4 epsilon chain antibody|T-cell surface glycoprotein CD3 epsilon chain antibody|T3E antibody|TCRE antibody|Anti-CD3 epsilon antibody [EP449E] (ab52959)
SCBT cat No: sc-20047|sc-1128|sc-137137|sc-30160|sc-1129|sc-26429|sc-26431|sc-18871|sc-1174|
CD3E Monoclonal Antibody
|Catalogue No.|| |
CD3E Monoclonal Antibody detects endogenous levels of CD3E protein.
Purified recombinant fragment of CD3E expressed in E Coli
WB, FC, ELISA
|Recommended dilution|| |
WB 1:500-1:2000; FC 1:200-1:400; ELISA 1:10000
CD3E Antibody was tube-contained. Ascitic fluid containing 0.03% sodium azide.
CD3E Antibody was purified using affinity purification.
-20 Celsius degree. Avoid repeated freeze/thaw cycles.
|Alternative antibody names|| |
T-cell surface glycoprotein CD3 epsilon chain antibody, T-cell surface antigen T3/Leu-4 epsilon chain antibody, CD antigen CD3e antibody
|Protein names|| |
T-cell surface glycoprotein CD3 epsilon chain , T-cell surface antigen T3/Leu-4 epsilon chain , CD antigen CD3e
|Protein function|| |
The CD3 complex mediates signal transduction, resulting in T-cell activation and proliferation. Required for normal immune responses .
|Involvement in disease|| |
Immunodeficiency 18 (IMD18) [MIM:615615]: An autosomal recessive primary immunodeficiency characterized by onset in infancy or early childhood of recurrent infections. The severity is variable, encompassing both a mild immunodeficiency and severe combined immunodeficiency (SCID), resulting in early death without bone marrow transplantation in some patients. Immunologic work-up of the IMD18 SCID patients shows a T cell-negative, B cell-positive, natural killer (NK) cell-positive phenotype, whereas T-cell development is not impaired in the mild form of IMD18. . Note: The disease is caused by mutations affecting the gene represented in this entry.
|Protein sequence and domain|| |
Contains 1 Ig-like (immunoglobulin-like) domain. / Contains 1 ITAM domain.
|Protein cellular localization|| |
Cell membrane / Single-pass type I membrane protein
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St John’s Laboratory Ltd.
|Product type|| |
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