Technical Data

H7959-86
Clone Type
Monoclonal
Host
Mouse
Source
Human
Isotype
IgG1,k
Clone Number
1B11
Applications
WB
Crossreactivity
Hu
Shipping Temp
Blue Ice
Storage Temp
-20°C
Mouse Anti-Huntingtin Interacting Protein 1 (HIP1, HIP I, ILWEQ, MGC126506)

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.

Cellular Localization: Localization: Cytoplasmic
Applications
Suitable for use in Western Blot. Other applications not tested.
Recommended Dilution
Optimal dilutions to be determined by the researcher.
Storage and Stability
May be stored at 4°C for short-term only. For long-term storage and to avoid repeated freezing and thawing, aliquot Store at -20°C. Aliquots are stable for at least 12 months at -20°C. For maximum recovery of product, centrifuge the original vial after thawing and prior to removing the cap. Further dilutions can be made in assay buffer.
Immunogen
Human 3'-HIP1 (~65 kDa).
Form
As reported
Purity
Ascites
Specificity
Specific for human HIP1. Does not crossreact with HIP1r. It does not appear to work in rat. Other species have not been tested.

Intended for research use only. Not for use in human, therapeutic, or diagnostic applications.

References
1. Rao, et al Mol. Cell. Bio. 21:7796-7806 (2001)|2. Saint-Dic, et al JBC. 276:21192-21198 (2001)|3. Rao, et al Can. Cell. 3:471-482 (2003)
USBio References
No references available
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