TRIM32 Antibody (N-term) Blocking peptide
Synthetic peptide
- SPECIFICATION
- CITATIONS
- PROTOCOLS
- BACKGROUND
Primary Accession | Q13049 |
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Clone Names | 100408318 |
Peptide ID | 100408318 |
Gene ID | 22954 |
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Other Names | E3 ubiquitin-protein ligase TRIM32, 632-, 72 kDa Tat-interacting protein, Tripartite motif-containing protein 32, Zinc finger protein HT2A, TRIM32, HT2A |
Target/Specificity | The synthetic peptide sequence used to generate the antibody AP13287a was selected from the N-term region of TRIM32. A 10 to 100 fold molar excess to antibody is recommended. Precise conditions should be optimized for a particular assay. |
Format | Synthetic peptide was lyophilized with 100% acetonitrile and is supplied as a powder. Reconstitute with 0.1 ml DI water for a final concentration of 1 mg/ml. |
Storage | Maintain refrigerated at 2-8°C for up to 6 months. For long term storage store at -20°C. |
Precautions | This product is for research use only. Not for use in diagnostic or therapeutic procedures. |
Name | TRIM32 |
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Synonyms | HT2A |
Function | Has an E3 ubiquitin ligase activity. Ubiquitinates DTNBP1 (dysbindin) and promotes its degradation. May ubiquitinate BBS2. May play a significant role in mediating the biological activity of the HIV-1 Tat protein in vivo. Binds specifically to the activation domain of HIV-1 Tat and can also interact with the HIV-2 and EIAV Tat proteins in vivo. |
Cellular Location | Cytoplasm. Note=Localized in cytoplasmic bodies, often located around the nucleus |
Tissue Location | Spleen, thymus, prostate, testis, ovary, intestine, colon and skeletal muscle |

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Background
The protein encoded by this gene is a member of thetripartite motif (TRIM) family. The TRIM motif includes threezinc-binding domains, a RING, a B-box type 1 and a B-box type 2,and a coiled-coil region. The protein localizes to cytoplasmicbodies. The protein has also been localized to the nucleus, whereit interacts with the activation domain of the HIV-1 Tat protein.The Tat protein activates transcription of HIV-1 genes. [providedby RefSeq].
References
Bailey, S.D., et al. Diabetes Care 33(10):2250-2253(2010)Liu, Y., et al. J. Invest. Dermatol. 130(5):1384-1390(2010)Talmud, P.J., et al. Am. J. Hum. Genet. 85(5):628-642(2009)Markson, G., et al. Genome Res. 19(10):1905-1911(2009)van Wijk, S.J., et al. Mol. Syst. Biol. 5, 295 (2009) :

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