NAC1 Antibody #4183
- WB
Supporting Data
REACTIVITY | M R |
SENSITIVITY | Endogenous |
MW (kDa) | 62 |
SOURCE | Rabbit |
Application Key:
- WB-Western Blotting
Species Cross-Reactivity Key:
- M-Mouse
- R-Rat
Product Information
Product Usage Information
Application | Dilution |
---|---|
Western Blotting | 1:1000 |
Storage
Protocol
Specificity / Sensitivity
NAC1 Antibody detects endogenous levels of total NAC1 protein in mouse and rat and weakly detects human NAC1 protein.
Species Reactivity:
Mouse, Rat
The antigen sequence used to produce this antibody shares 100% sequence homology with the species listed here, but reactivity has not been tested or confirmed to work by CST. Use of this product with these species is not covered under our Product Performance Guarantee.
Species predicted to react based on 100% sequence homology:
Human
Source / Purification
Polyclonal antibodies are produced by immunizing animals with a synthetic peptide corresponding to the amino acid sequence surrounding Ala321 of human NAC1 protein. Antibodies are purified by protein A and peptide affinity chromatography.
Background
NAC1 or nuclear accumbens-1 is a nuclear factor that belongs to the POZ/BTB (Pox virus and zinc finger/bric-a-brac tramtrack broad complex) domain family. Also known as BTBD14B, it was originally identified in a unique neuronal forebrain structure responsible for reward motivation and addictive behaviors (1,2). NAC1 recruits HDAC3 and HDAC4 to transcriptionally repress gene expression in neuronal cells (3) and specifically co-represses other POZ/BTB proteins in the central nervous system (4). NAC1 is upregulated in several tumor types, including breast, renal cell, and hepatocellular carcinoma, as well as high grade ovarian serous carcinoma, where it has long been suspected as a chemoresistance gene (5,6). The chemoresistance mechanism reportedly occurs through NAC1 negative regulation of the GADD45 pathway (7). NAC1 has also been described as part of the extended transcriptional network in pluripotent cells that involves Oct-4, Sox2, Nanog, Sall1, KLF4 and Sall4 (8).
- Kalivas, P.W. et al. (1999) Synapse 33, 153-9.
- Mackler, S.A. et al. (2000) J Neurosci 20, 6210-7.
- Korutla, L. et al. (2005) J Neurochem 94, 786-93.
- Korutla, L. et al. (2009) Neurochem Int 54, 245-52.
- Nakayama, K. et al. (2006) Proc Natl Acad Sci USA 103, 18739-44.
- Yeasmin, S. et al. (2008) Clin Cancer Res 14, 1686-91.
- Jinawath, N. et al. (2009) Oncogene 28, 1941-8.
- Kim, J. et al. (2008) Cell 132, 1049-61.
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