購物車
幫助
021-54845833/15800441009
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Background: |
This gene is one of the contiguous genes at 7q11.23 commonly deleted in Williams syndrome, a multisystem developmental disorder. This gene consists of at least 14 exons, and its alternative splicing generates 3 transcript variants, all encoding the same protein. Involved in FCER1 (high affinity immunoglobulin epsilon receptor)-mediated signaling in mast cells. May also be involved in BCR (B-cell antigen receptor)-mediated signaling in B-cells and FCGR1 (high affinity immunoglobulin gamma Fc receptor I)-mediated signaling in myeloid cells. Couples activation of these receptors and their associated kinases with distal intracellular events through the recruitment of GRB2. |
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Applications: |
ELISA, IHC |
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Name of antibody: |
LAT2 |
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Immunogen: |
Fusion protein of human LAT2 |
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Full name: |
linker for activation of T cells family, member 2 |
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Synonyms： |
LAB, NTAL, WSCR5, WBSCR5, HSPC046, WBSCR15 |
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SwissProt: |
Q9GZY6 |
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ELISA Recommended dilution: |
1000-5000 |
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IHC positive control: |
Human colon cancer |
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IHC Recommend dilution: |
10-50 |
