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About This Item
NACRES:
NA.41
UNSPSC Code:
12352203
Conjugate:
unconjugated
Clone:
polyclonal
Application:
ELISA (i), IHC, WB
Citations:
6
biological source
rabbit
conjugate
unconjugated
antibody form
saturated ammonium sulfate (SAS) precipitated
antibody product type
primary antibodies
clone
polyclonal
form
buffered aqueous solution
species reactivity
human
technique(s)
immunohistochemistry: 1:50-1:100, indirect ELISA: 1:1000, western blot: 1:100-1:500
NCBI accession no.
shipped in
dry ice
storage temp.
−20°C
target post-translational modification
unmodified
Gene Information
human ... CHIP(10273)
General description
CHIP (C-terminus of HSP70-interacting protein) gene is located in human chromosome 16p13.3. This gene codes for a E3 ubiquitin ligase. The bioactive site of the protein includes three tandem repeats of the tetratricopeptide motif at the N-terminal, a C-terminal U-box domain and a charged coiled-coil region in between the two. CHIP is ubiquitously expressed.
CHIP is an E3 ligase for nNOS whose action is facilitated by (and possibly requires) its interaction with nNOS-bound hsp70. Co-chaperone CHIP, possibly with another E3 ligase(s), modulates the ubiquitylation of mutant Cu/Zn-superoxide dismutase and renders them more susceptible for proteasomal degradation. CHIP functions as a negative regulator of AR transcriptional activity by promoting AR degradation. CHIP-Hsc70 complex ubiquitinates phosphorylated tau and enhances cell survival. CHIP can interact with the Smad1/Smad4 proteins and block BMP signal transduction through the ubiquitin-mediated degradation of Smad proteins. CHIP E3 controls both the association of Hsp70/Hsp90 chaperones with ErbB2 and the down-regulation of ErbB2 induced by inhibitors of Hsp90. CHIP is associated with Parkin and enhances its ubiquitin ligase activity related to Parkinson′s disease.
Immunogen
CHIP (Q969U2, 208-242)
This antibody is generated from rabbits immunized with a KLH conjugated synthetic peptide at the C-term of human CHIP (STUB1).
This antibody is generated from rabbits immunized with a KLH conjugated synthetic peptide at the C-term of human CHIP (STUB1).
Biochem/physiol Actions
CHIP (C-terminus of HSP70-interacting protein) induces ubiquitination and proteasomal degradation of proteins sent by chaperone partners for removal via endocytic-lysosomal machinery. CHIP interacts with molecular chaperones and degradation machineries to maintain protein homeostasis within the cell. Lack of CHIP increases the process of aging, indicating that the gene might mediate long living. CHIP prevents the accumulation of protein aggregates in age-related disease conditions. CHIP is responsible for the degradation of CD166, a cancer stem-like cell (CSC) marker in head and neck cancer. Therefore, CHIP is suggested as an option for the diagnosis of head and neck cancer.
Physical form
Purified polyclonal antibody supplied in PBS with 0.09% (W/V) sodium azide.
Disclaimer
Unless otherwise stated in our catalog or other company documentation accompanying the product(s), our products are intended for research use only and are not to be used for any other purpose, which includes but is not limited to, unauthorized commercial uses, in vitro diagnostic uses, ex vivo or in vivo therapeutic uses or any type of consumption or application to humans or animals.
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Storage Class
10 - Combustible liquids
wgk
nwg
flash_point_f
Not applicable
flash_point_c
Not applicable
Regulatory Information
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Find documentation for the products that you have recently purchased in the Document Library.
Molecular Chaperone HSP90 Is Necessary to Prevent Cellular Senescence via Lysosomal Degradation of p14ARF.
Han SY
Cancer Research, 77(2), 343-354 (2017)
BAG2 Interferes with CHIP-Mediated Ubiquitination of HSP72.
Schonbuhler B
International Journal of Molecular Sciences, 18(1), 1-10 (2016)
Cancer stem-like cell related protein CD166 degrades through E3 ubiquitin ligase CHIP in head and neck cancer.
Xiao M
Experimental Cell Research, 353(1), 46-53 (2017)
The Ubiquitin Ligase CHIP Integrates Proteostasis and Aging by Regulation of Insulin Receptor Turnover.
Tawo R
Cell, 169(3), 470-482 (2017)
Identification of CHIP as a novel causative gene for autosomal recessive cerebellar ataxia.
Shi Y
PLoS ONE, 101, 236-244 (2013)
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