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H7960-01 Mouse Anti-Huntingtin Protein, aa2703-2911 (Huntington Disease)

Specifications
References
Clone Type
Monoclonal
Host
Mouse
Source
Human
Swiss Prot
P42858
Isotype
IgG1
Clone Number
3H2241 (HDC8A4)
Grade
Affinity Purified
Applications
IHC IP WB
Crossreactivity
Hu Mo Rb
Shipping Temp
Blue Ice
Storage Temp
-20°C

Huntington's disease (HD) is a neurodegenerative disorder caused by an expanding polyglutamine repeat in the huntingtin gene. HD is a mid-life onset autosomal dominant neurodegeneative disease that is characterized by psychiatric disorders, dementia, and involuntary movements (chorea), leading to death in 10-20 years.

Applications
Suitable for use in Immunohistochemistry, Immunoprecipitation and Western Blot. Other applications not tested.
Recommended Dilutions
Immunohistochemistry: Frozen. Increased cytoplasmic staining, relative to nuclear, has been reported using formaldehyde as a fixative compared with acetone/methanol. Optimal dilutions to be determined by the researcher.
Recommended Positive Control Tissue
Brain
Recommended Secondary Antibody
I1904-65W: IgG, F(ab’)2 (HRP) Pab Rb x Mo
Storage and Stability
May be stored at 4°C for short-term only. Aliquot to avoid repeated freezing and thawing. Store at -20°C. Aliquots are stable for 12 months after receipt. For maximum recovery of product, centrifuge the original vial after thawing and prior to removing the cap.
Immunogen
Recombinant protein corresponding to aa2703-2911 of human Huntingtin Protein.
Form
Supplied as a liquid in PBS, 0.09% sodium azide.
Purity
Purified by Protein G affinity chromatography.
Specificity
Recognizes an epitope corresponding to the human HDC region (aa2703-2911) of the Huntingtin protein. Detects a 350kD band on Western Blots but also detects smaller degradation products of Huntingtin. Recognizes both denatured and native Huntingtin in human brain. The combined use of H7960-01, H7960 and H7960-01A demonstrate that huntingtin is enriched in neuronal cells in the brain. Species Crossreactivity: rabbit and mouse.
References
1. Wilkinson, F.L., et al., Molecular Brain Research. 69: 10-20 (1999). 2. Yao Y et al. (2015) A striatal-enriched intronic GPCR modulates huntingtin levels and toxicity. Elife. 4: 4. 3. Jones, A.L. (1999) The localization and interactions of huntingtin. Philos Trans R Soc Lond B Biol Sci. 354 (1386): 1021-7. 4. Lazzeroni G et al. (2013) A phenotypic screening assay for modulators of huntingtin-induced transcriptional dysregulation. J Biomol Screen. 18 (9): 984-96. 5. Li X et al. (2008) A function of huntingtin in guanine nucleotide exchange on Rab11. Neuroreport. 19 (16): 1643-7.
USBio References
No references available
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