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Key Documents

A5968

Sigma-Aldrich

Anti-AP-1 antibody produced in rabbit

affinity isolated antibody, buffered aqueous solution

Synonym(s):

Ap-1 Antibody, Ap1 Antibody, Ap1 Antibody - Anti-AP-1 antibody produced in rabbit, Anti-c-Jun

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About This Item

MDL number:
UNSPSC Code:
12352203
NACRES:
NA.41

biological source

rabbit

conjugate

unconjugated

antibody form

affinity isolated antibody

antibody product type

primary antibodies

clone

polyclonal

form

buffered aqueous solution

mol wt

antigen 39 kDa

species reactivity

human

technique(s)

immunohistochemistry (formalin-fixed, paraffin-embedded sections): 1:200 using formalin-fixed, paraffin-embedded sections of human colon carcinoma
microarray: suitable
western blot: 1:200 using HeLa nuclear extract

UniProt accession no.

shipped in

dry ice

storage temp.

−20°C

target post-translational modification

unmodified

Gene Information

human ... JUN(3725)

General description

Activation Protein transcription factor 1 (AP-1) is a leucine zipper transcription factor that recognizes a specific palindromic sequence present in several promoters and enhancers. AP-1 can be induced by several growth and apoptosis-related signaling pathways. Jun proteins are also involved in metastatic, inflammatory and stress responses.
Anti-AP-1/c-Jun recognizes an epitope located on the c-Jun DNA binding domain. This epitope is highly conserved in c-Jun, Jun B and Jun D proteins of chicken, mouse, rat, and human. By immunoblotting, the antibody reacts specifically with AP-1/c-Jun (a single band or occasionally a doublet at 39kDa region). Additional bands of lower molecular weight may be observed. Staining of AP-1/c-Jun band(s) is inhibited by the AP-1/c-Jun immunizing peptide (amino acid residues 246-263).
Activation Protein transcription factor 1 (AP-1) is a regulatory leucine zipper transcription factor. AP-1 is composed of either a homodimer of two Jun protein molecules or a heterodimer of one Jun and one Fos (Proto-oncogenes) molecules.

Immunogen

synthetic peptide corresponding to amino acids 246-263 of human c-Jun with N-terminally added lysine, conjugated to KLH.

Application

Anti-AP-1 antibody has been used in
  • immunohistochemistry
  • immunochemistry
  • western blotting

Immunofluorescence of Hela cells was performed using monoclonal anti-AP1 (clone 100/3) as the primary antibody.

Biochem/physiol Actions

Activation Protein transcription factor 1 (AP-1) recognizes a specific sequence (TPA response element, a palindromic TRE sequence TGA(C/G) TCA or related sequences) present in many promoter and enhancer gene regions. Regulation of AP-1 is achieved by changes in the expression of Jun and Fos proteins in the dimer, by phosphorylation at both Ser63 and Ser73 by c-Jun N-terminal kinases (JNK) and by interaction with a variety of transcriptional coactivators like C-Jun activation domain-binding protein-1 (JAB1). AP-1 is induced by a variety of signals including those eliciting proliferation, differentiation and apoptosis.

Physical form

Solution in 0.01 M phosphate buffered saline, pH 7.4, containing 1% bovine serum albumin and 15 mM 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 Code

10 - Combustible liquids

WGK

WGK 3

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable


Certificates of Analysis (COA)

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P Angel et al.
Nature, 332(6160), 166-171 (1988-03-10)
Proto-oncogenes encode proteins with three main sites of action: the cell-surface membrane, the cytoplasm and the nucleus. Although the exact biochemical function of most proto-oncogene products is not understood, several of them are known to be involved in signal transduction.
Samuel Jang et al.
Cancer medicine, 6(9), 2142-2152 (2017-08-05)
Notch signaling is minimally active in neuroendocrine (NE) cancer cells. While histone deacetylase inhibitors (HDACi) suppress NE cancer growth by inducing Notch, the molecular mechanism underlying this interplay has not yet been defined. NE cancer cell lines BON, H727, and
Jiping Da et al.
Critical care medicine, 35(1), 26-32 (2006-11-11)
Nitric oxide inhibits the expression of many genes involved in inflammatory diseases. Glucocorticoids inhibit similar transcription factors. We hypothesized that there may be an interaction between nitric oxide and glucocorticoids, with the potential to enhance the anti-inflammatory effect when administered
AP-1 function and regulation
Karin M, et al.
Current Opinion in Cell Biology, 9(2), 240-246 (1997)
Twelve hours of heat stress induces inflammatory signaling in porcine skeletal muscle
Ganesan S, et al.
The American Journal of Physiology, 310(11), R1288-R1296 (2016)

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