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FIGURE: 1 / 1
Positive Samples: U-87MG, 293T, HeLa, Mouse brain, Mouse spleen, Mouse liver, Rat brain
Immunogen sequence: KPVVVIPEEA PEDEEPENLI EISTGPPAGE PVVVADLFDQ TFGPPNGSVK DDRDLQIESL KREVEMLRSE LEKIKLEAQR YIAQLKSQVN ALEGELEEQR KQKQKALVDN EQLRHELAQL RAAQLEGERS QGLREEAERK ASATEARYNK LKEKHSELVH VHAELLRKNA DTAKQLTVTQ QSQEEVARVK EQLAFQVEQV KRESELKLEE KSDQLEKLKR ELEAKAGELA RAQEALSHTE QSKSELSSRL DTLSAEKDAL SGAVRQREAD LLAAQSLVRE TEAALSREQQ RSSQEQGELQ G
Huntingtin disease, a neurodegenerate disease, is caused by the expansion of a polymorphic glutamine tract in huntingtin. The Huntingtin Interacting Protein 1 (HIP-1) is a reportedly proapoptotic, cargo-specific adaptor protein that may be involved in the pathogenesis of Huntingtin disease. As well as playing a role in Huntingtin disease, it is likely to be involved in the recruitment of clathrin coats to lipid membranes and it may also factor in tumorigenesis by allowing the survival of precancerous and cancerous cells. Since HIP-1 expression is significantly associated with prostate and colon cancer metastasis, HIP-1 can serve as a putative prognostic factor for prostate and colon cancers.
⚠WARNING: This product can expose you to chemicals including mercury, which is known to the State of California to cause birth defects or other reproductive harm. For more information go to www.P65Warnings.ca.gov.
For Research Use Only. Not for use in diagnostic procedures. Not for resale without express authorization.
Protein Aliases: HIP-12; HIP1-related protein; huntingtin interacting protein 12; Huntingtin-interacting protein 1-related protein; Huntingtin-interacting protein 12
Gene Aliases: AA410023; HIP12; HIP1R; HIP3; ILWEQ; KIAA0655; mKIAA0655
UniProt ID: (Human) O75146, (Mouse) Q9JKY5
Entrez Gene ID: (Human) 9026, (Mouse) 29816, (Rat) 81917
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