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Huntingtin Antibody

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Product Details

Summary
Product Discontinued
View other related Huntingtin Primary Antibodies

Order Details


    • Catalog Number
      NBP1-03377
    • Availability
      Product Discontinued

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Huntingtin Antibody Summary

Immunogen
A synthetic peptide from internal part of rat Huntingtin (Huntington disease protein homolog, Htt, HD protein homolog) conjugated to an immunogenic carrier protein was used as the immunogen. The antigen shares 87% identity with mouse and human sequences.
Localization
subcellular location: cytoplasm. nucleus. tissue specificity: expressed to a high degree in all the regions of the brain of adults and in meiotic cells of the testis.
Specificity
Huntingtin.
Clonality
Polyclonal
Host
Rabbit
Gene
HTT
Purity
Unpurified
Innovator's Reward
Test in a species/application not listed above to receive a full credit towards a future purchase.

Applications/Dilutions

Dilutions
  • Immunocytochemistry/ Immunofluorescence 1:10-1:500
  • Immunohistochemistry 1:10-1:500
  • Immunohistochemistry-Frozen 1:10-1:500
  • Immunohistochemistry-Paraffin 1:10-1:500
  • Western Blot 1:300-1:1000

Reactivity Notes

Rat and Mouse.

Packaging, Storage & Formulations

Storage
Store at 4C short term. Aliquot and store at -20C long term. Avoid freeze-thaw cycles.
Buffer
Whole antisera
Preservative
No Preservative
Concentration
LYOPH
Purity
Unpurified
Reconstitution Instructions
Reconstitute with 0.1 ml sterilized water to desired concentration.

Alternate Names for Huntingtin Antibody

  • HD protein
  • HD
  • HTT
  • huntingtin (Huntington disease)
  • Huntingtin
  • IT15
  • IT15HDHuntington disease protein

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.

Limitations

This product is for research use only and is not approved for use in humans or in clinical diagnosis. Primary Antibodies are guaranteed for 1 year from date of receipt.

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Product General Protocols

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Video Protocols

WB Video Protocol
ICC/IF Video Protocol

FAQs for Huntingtin Antibody (NBP1-03377) (0)

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Secondary Antibodies

 

Isotype Controls

Additional Huntingtin Products

Research Areas for Huntingtin Antibody (NBP1-03377)

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Blogs on Huntingtin.

Mechanisms of Neurodegeneration: Protein aggregation and failure of autophagy
By Michalina Hanzel, PhDIn a series of three blog posts I will briefly explore the major cellular mechanisms responsible for many neurodegenerative disorders. The first, and perhaps the most apparent, is the accumulat...  Read full blog post.

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Bioinformatics

Gene Symbol HTT
Entrez
Uniprot