AV38530
Anti-HDAC1 antibody produced in rabbit
IgG fraction of antiserum
Synonym(s):
Anti-Histone deacetylase 1
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About This Item
Recommended Products
biological source
rabbit
Quality Level
conjugate
unconjugated
antibody form
IgG fraction of antiserum
antibody product type
primary antibodies
clone
polyclonal
form
buffered aqueous solution
mol wt
55 kDa
species reactivity
dog, bovine, human, guinea pig, rat, mouse
concentration
0.5 mg - 1 mg/mL
technique(s)
western blot: suitable
NCBI accession no.
UniProt accession no.
shipped in
wet ice
storage temp.
−20°C
target post-translational modification
unmodified
Gene Information
human ... HDAC1(3065)
General description
Histone deacetylase 1 (HDAC1) is involved in the regulation of eukaryotic gene expression. HDAC1 is involved in the regulation of critical cell processes such as cell proliferation, differentiation and apoptosis. HDAC1 in association with other gene regulatory proteins regulates a wide range of specific gene cascades. For example HDAC1 is a regulator of retrotransposon expression in mouse embryonic stem cells. HDAC1 is the target of various histone deacetylase inhibitor under development as potential cancer therapeutic agent.
Specificity
Anti-HDAC1 polyclonal antibody reacts with canine, human, mouse, rat, and bovine histone deacetylase 1 proteins.
Immunogen
Synthetic peptide directed towards the C terminal region of human HDAC1
Application
Anti-HDAC1 polyclonal antibody is used to tag histone deacetylase 1 protein for detection and quantitation by Western blotting and in plasma by immunohistochemical (IHC) techniques. It is used as a probe to determine the roles of histone deacetylase 1 in a variety of gene activation cascades and cellular processes.
Biochem/physiol Actions
Histone acetylation and deacetylation, catalyzed by multisubunit complexes, play a key role in the regulation of eukaryotic gene expression. HDAC1 belongs to the histone deacetylase/acuc/apha family and is a component of the histone deacetylase complex. HDAC1 also interacts with retinoblastoma tumor-suppressor protein and this complex is a key element in the control of cell proliferation and differentiation. Together with metastasis-associated protein-2, HDAC1 deacetylates p53 and modulates its effect on cell growth and apoptosis.Histone acetylation and deacetylation, catalyzed by multisubunit complexes, play a key role in the regulation of eukaryotic gene expression. The protein encoded by this gene belongs to the histone deacetylase/acuc/apha family and is a component of the histone deacetylase complex. It also interacts with retinoblastoma tumor-suppressor protein and this complex is a key element in the control of cell proliferation and differentiation. Together with metastasis-associated protein-2, it deacetylates p53 and modulates its effect on cell growth and apoptosis.
Sequence
Synthetic peptide located within the following region: SDSEEEGEGGRKNSSNFKKAKRVKTEDEKEKDPEEKKEVTEEEKTKEEKP
Physical form
Purified antibody supplied in 1x PBS buffer with 0.09% (w/v) sodium azide and 2% sucrose.
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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Description
Pricing
Storage Class Code
10 - Combustible liquids
WGK
WGK 1
Flash Point(F)
Not applicable
Flash Point(C)
Not applicable
Certificates of Analysis (COA)
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Ilenia Aversa et al.
International journal of molecular sciences, 19(10) (2018-10-03)
Nuclear Factor-κB (NF-κB) is frequently activated in tumor cells contributing to aggressive tumor growth and resistance to chemotherapy. Here we demonstrate that Ferritin Heavy Chain (FHC) protein expression inversely correlates with NF-κB activation in cancer cell lines. In fact, FHC
Emma L Smith et al.
Nucleic acids research, 47(21), 11151-11163 (2019-10-11)
Phosphorylation of the NF-κB transcription factor is an important regulatory mechanism for the control of transcription. Here we identify serine 80 (S80) as a phosphorylation site on the p50 subunit of NF-κB, and IKKβ as a p50 kinase. Transcriptomic analysis
Fa-Xiu Chen et al.
International journal of biological sciences, 16(9), 1481-1494 (2020-04-01)
Inflammation and apoptosis are considered as two major pathological causes of human sarcopenia. The current understanding based on different models recognizes that apoptosis does not trigger inflammation, while emerging evidence indicates that inflammation can induce apoptosis. Here, we provide solid
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