
Thermo Fisher Scientific HAP1 Polyclonal Antibody
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Applications
Tested Dilution
Publications
Western Blot (WB)
1:300-1:2,000
Immunohistochemistry (IHC)
1:300-1:2,000
Miscellaneous PubMed (Misc)
-
View 2 publications 2 publications
Product Specifications
Species Reactivity
Mouse, Rat
Published species
Not Applicable
Host/Isotype
Rabbit / Ig
Class
Polyclonal
Type
Antibody
Immunogen
A synthetic peptide from the n-terminal of rat HAP 1 conjugated to blue carrier protein was used as the antigen if (typeof window.$mangular === undefined
|| !window.$mangular) { window.$mangular = {}; } $mangular.antigenJson = \[{
targetFamily:
HAP1,
uniProtId:
P54256-1,
ncbiNodeId:
10114,
antigenRange:
1,
antigenLength:
629,
antigenImageFileName:
OSH00008W-100UL_HAP1_P54256-1_Rabbit.svg,
antigenImageFileNamePDP:
OSH00008W-100UL_HAP1_P54256-1_Rabbit_PDP.jpeg,
sortOrder:
3}\]
; $mangular.isB2BCMGT = false
; $mangular.isEpitopesModalImageMultiSizeEnabled = true
;
View immunogen .st0{fill:#FFFFFF;} .st1{fill:#1E8AE7;}
Conjugate
Unconjugated Unconjugated Unconjugated
Form
Lyophilized
Concentration
Conc. Not Determined
Storage buffer
whole serum
Contains
no preservative
Storage conditions
Store at 4°C short term. For long term storage, store at -20°C, avoiding freeze/thaw cycles. Glycerol (1:1) may be added for added stability.
Shipping conditions
Ambient (domestic); Wet ice (international)
Product Specific Information
Reconstitute in 100 µL of sterile water. Centrifuge to remove any insoluble material.
The peptide shares 95% identity with mouse sequence.
Specificity of this antibody: HAP1.
Target Information
Huntington`s disease (HD), a neurodegenerative disorder characterized by loss of striatal neurons, is caused by an expansion of a polyglutamine tract in the HD protein huntingtin. HAP1 was initially identified through a two-hybrid library screening; the binding of HAP1 to huntingtin correlated with the expansion of the polyglutamine tract. HAP1 also interacts with two cytoskeletal proteins (dynactin and pericentriolar autoantigen protein 1), suggesting that HAP1 may play a role in vesicular trafficking or organelle transport. HAP1 is also involved with the huntingtin-enhanced BDNF transport along the cellular microtubles. Attenuation of this process led to the loss of neurotrophic support and neuronal toxicity, which suggests that loss of this function might contribute to pathogenesis. Several alternatively spliced isoforms have been described for HAP1.
For Research Use Only. Not for use in diagnostic procedures. Not for resale without express authorization.
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