Anti-HTT Monoclonal Antibody (3B5H10)

Anti-HTT Monoclonal Antibody (3B5H10)

Cat No: ASPC007

Summary
Host Species:
Mouse
Species Reactivity:
Human
Applications:
Immunoprecipitation, Immunofluorescence, Electron Microscopy, Immunohistochemistry, Inhibition, Western Blot
Clone ID:
3B5H10
Clonality:
Monoclonal

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Product Information
Subcat Description Isotype Antibody Modification Conjugate Size Price Availability Quantity
ASPC007 Anti-HTT Antibody (3B5H10) Mouse IgG1, Lambda None $460 4-6 weeks
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ASPC007-2 Anti-HTT Antibody (3B5H10), scFv fragment Mouse scFv His tag None $460 In stock
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ASPC007-P Anti-HTT Antibody (3B5H10), PE Mouse IgG1, Lambda PE $1,180 2-3 weeks
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ASPC007-A Anti-HTT Antibody (3B5H10), APC Mouse IgG1, Lambda APC $980 2-3 weeks
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ASPC007-H Anti-HTT Antibody (3B5H10), HRP Mouse IgG1, Lambda HRP $600 2-3 weeks
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ASPC007-B Anti-HTT Antibody (3B5H10), Biotin Mouse IgG1, Lambda Biotin $680 2-3 weeks
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Custom Antibody We can also offer conjugation antibodies (Alexa Fluor, Cy, APC, etc.) and other format antibodies (low endotoxin, Fab, scFv, etc.)

  • Anti-HTT Monoclonal Antibody (3B5H10)
    • Product Description:
      3B5H10 specifically binds to polyglutamine (polyQ) tracts. These expanded polyQ tracts are associated with the pathogenesis of Huntington's disease and other polyglutamine disorders. This antibody does not recognize normal, non-pathogenic forms of huntingtin, making it particularly useful for detecting disease-relevant protein forms.
      Applications:
      Immunoprecipitation, Immunofluorescence, Electron Microscopy, Immunohistochemistry, Inhibition, Western Blot
      Source:
      Mouse
      Target:
      HTT
      Target Species:
      Human
      Specificity:
      This antibody recognizes extended polyglutamine repeats (polyQ) in mutant huntingtin.
      Immunogen:
      A fragment of human Huntingtin, consisting of the N-terminal 1-171 amino acids, with a polyglutamine stretch of 68 residues.
      Clonality:
      Monoclonal
      Clone ID:
      3B5H10
      Isotype:
      Mouse IgG1, Lambda
      Purification:
      The antibody was purified by Protein A.
      Purity:
      >95% as determined by SDS-PAGE
      Aggregation:
      <5% as determined by SEC
      Concentration:
      1 mg/mL
      Form:
      Liquid
      Endotoxin:
      Please contact us for more information.
      Formulation:
      Contact us for customized product form or formulation.
      Preservative:
      BSA and Azide free.
      Stabilizer:
      None
      Shipping:
      Shipped at 4°C.
      Storage:
      This antibody can be store at 2°C-8°C for one month. Upon delivery aliquot. For longer storage, store at -20°C. Avoid repeated freeze-thaw cycles.
  • Anti-HTT Monoclonal Antibody (3B5H10) Applications
    • Note:
      Optimal dilutions/concentrations should be determined by the end user.
Gene Symbol
HTT
Protein Name
Huntingtin
Introduction
Huntingtin is a disease gene linked to Huntington's disease, a neurodegenerative disorder characterized by loss of striatal neurons. This is thought to be caused by an expanded, unstable trinucleotide repeat in the huntingtin gene, which translates as a polyglutamine repeat in the protein product. A fairly broad range of trinucleotide repeats (9-35) has been identified in normal controls, and repeat numbers in excess of 40 have been described as pathological. The huntingtin locus is large, spanning 180 kb and consisting of 67 exons. The huntingtin gene is widely expressed and is required for normal development. It is expressed as 2 alternatively polyadenylated forms displaying different relative abundance in various fetal and adult tissues. The larger transcript is approximately 13.7 kb and is expressed predominantly in adult and fetal brain whereas the smaller transcript of approximately 10.3 kb is more widely expressed. The genetic defect leading to Huntington's disease may not necessarily eliminate transcription, but may confer a new property on the mRNA or alter the function of the protein. One candidate is the huntingtin-associated protein-1, highly expressed in brain, which has increased affinity for huntingtin protein with expanded polyglutamine repeats. This gene contains an upstream open reading frame in the 5' UTR that inhibits expression of the huntingtin gene product through translational repression.
Alternative Names
Huntingtin; Huntington Disease Protein; IT15; HD; Huntingtin (Huntington Disease); HD Protein; LOMARS
Gene ID
UniProt
Related Disease
Huntington disease (HD)
Subcellular Location
Nucleoplasm,Cytosol
Tissue Specificity
Expressed in the brain cortex (at protein level). Widely expressed with the highest level of expression in the brain (nerve fibers, varicosities, and nerve endings). In the brain, the regions where it can be mainly found are the cerebellar cortex, the neocortex, the striatum, and the hippocampal formation.
Cell Type
B cells, T cells, Thymocytes, Tregs
Function
May play a role in microtubule-mediated transport or vesicle function.
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