Huntingtin (HTT) Mouse Monoclonal Antibody [Clone ID: HDB4E10]

CAT#: SM1661

Huntingtin (HTT) mouse monoclonal antibody, clone HDB4E10, Purified

Product Images

Total protein extract of normal human cerebral cortex separated as a strip on a 3- 12.5% gradient SDS-PAGE gel and Western blotted. The blot was probed with.

Specifications

Product Data

• Clone Name: HDB4E10
• Applications: IHC, IP, WB
• Recommended Dilution: Western blot: Clone HDB4E10 detects a 350KD band on western blots but also detects smaller degradation products of huntingtin.
  Immunoprecipitation.
  Immunohistochemistry on Frozen Sections: Increased cytoplasmic staining, relative to nuclear, has been reported using formaldehyde as a fixative compared with acetone/methanol, See Wilkinson et al.
  Recommended Positive Control tissue: Brain.
• Reactivities: Human, Mouse, Rabbit
• Host: Mouse
• Isotype: IgG1
• Clonality: Monoclonal
• Immunogen: Recombinant protein corresponding to amino acids 1844-2131 of Huntingtin
• Specificity: This antibody reacts with an epitope corresponding to the HDB region (amino acids 1844-2131) of the Huntingtin protein.
  The combined use of Clone HDB4E10 (Cat.-No SM1661), HDC8A4 (Cat.-No SM1662) and HDA3E10 (Cat.-No SM1660) demonstrate that huntingtin is enriched in neuronal cells in the brain.
• Formulation: PBS
  State: Purified
  State: Liquid purified IgG fraction
  Preservative: 0.09% Sodium Azide
• Concentration: lot specific
• Conjugation: Unconjugated
• Storage: Store undiluted at 2-8°C for one month or (in aliquots) at -20°C for longer.
  Avoid repeated freezing and thawing.
• Stability: Shelf life: one year from despatch.
• Gene Name: huntingtin
• Database Link:
  Entrez Gene 3064 Human
  UniProt ID P42858
• Background: 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. The HD gene product is widely expressed in human tissues, with the highest level of expression in the brain. The huntingtin gene product is expressed at similar levels in patients and controls, which suggests that the expansion of the polyglutamine repeat induces a toxic gain of function perhaps through interactions with other cellular proteins. Using yeast two-hybrid system, HAP1 (huntingtin associated protein 1) has been identified, that associates with huntingtin protein. The In vitro data suggest that the association between HAP1 and huntingtin is enhanced by increasing length of glutamine repeat.
• Synonyms: Huntington Disease Protein, HD, IT15, HTT