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- goat polyclonal IgG, 200µg/ml
- epitope mapping within an internal region of TIS11D of human origin
- recommended for detection of TIS11D of mouse, rat and human origin by WB, IP, IF and ELISA; also reactive with additional species, including canine, bovine and porcine
- TransCruz reagent for Gel Supershift and ChIP applications, sc-79154 X, 200 µg/0.1 ml
- blocking peptide, sc-79154 P
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Ordering Information
Recommended Support Products:
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| Species |
Gene Name |
Gene ID |
Chromosome Location |
Isoform (mRNA) Accession # |
Protein Accession # |
OMIM™ Number |
| Human |
ZFP36L2 |
678 |
2p21 |
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P47974
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n/a |
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TIS11D Background Information
TIS11D, also known as ZFP36LA (zinc finger protein 36, C3H type-like 2), BRF2 (butyrate response factor 2), ERF2 or RNF162C, is a 494 amino acid protein that localizes to the nucleus and contains two CSH1-type zinc fingers. Belonging to the TIS11 family of early response proteins, TIS11D is thought to function as a nuclear transcription factor that binds to 5'UUAUUUAUUU-3' core RNA sequences and may regulate growth factor-induced cellular responses. The gene encoding TIS11D maps to human chromosome 2, which houses over 1,400 genes and comprises nearly 8% of the human genome. Harlequin icthyosis, a rare and morbid skin deformity, is associated with mutations in the ABCA12 gene, while the lipid metabolic disorder sitosterolemia is associated with defects in the ABCG5 and ABCG8 genes. Additionally, an extremely rare recessive genetic disorder, Alström syndrome, is caused by mutations in the ALMS1 gene, which maps to chromosome 2. |
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TIS11D (P-16)
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TIS11D (P-16): sc-79154. Western blot analysis of TIS11D expression in non-transfected: sc-117752 (A) and human TIS11D transfected: sc-174242 (B) 293T whole cell lysates. |
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