PMAIP1

The following PMAIP1 reagents supplied by CUSABIO are manufactured under a strict quality control system. Multiple applications have been validated and solid technical support is offered.

PMAIP1 Antibodies

PMAIP1 Antibodies for Homo sapiens (Human)

PMAIP1 Antibodies for Mus musculus (Mouse)

PMAIP1 Proteins

PMAIP1 Proteins for Rattus norvegicus (Rat)

PMAIP1 Proteins for Mus musculus (Mouse)

PMAIP1 Proteins for Homo sapiens (Human)

PMAIP1 Proteins for Canis lupus familiaris (Dog) (Canis familiaris)

PMAIP1 Background

Phorbol-12-myristate-13-acetate-induced protein 1 is a protein in humans that is encoded by PMAIP1 gene [1]. It is also known as Noxa [2]. PMAIP1/Noxa is a pro-apoptotic member of the Bcl-2 protein family [3]. Bcl-2 family members can form hetero- or homodimers, and they act as anti- or pro-apoptotic regulators that are involved in a wide variety of cellular activities. The expression of Noxa is regulated by the tumor suppressor p53, and Noxa has been shown to be involved in p53-mediated apoptosis. PMAIP1/Noxa promotes mitochondrial membrane changes and efflux of apoptogenic proteins from the mitochondria and contributes to p53/TP53-dependent apoptosis after radiation exposure. It also facilitates proteasomal degradation of MCL1. Through competition with BAK1 for binding to MCL1, PMAIP1/Noxa can displace BAK1 from its binding site on MCL1 (By similarity). Hyunhee Do et al. observed that overexpressed TFAP2C resulted in inhibition of GADD45B and PMAIP1 expressions at both the mRNA and protein levels in NSCLC cells. In addition, downregulation of GADD45B and PMAIP1 by TFAP2C promoted cell proliferation and cell motility, which are closely associated with NSCLC tumorigenesis [4].

[1] Hijikata M, Kato N, Sato T, Kagami Y, Shimotohno K (October 1990). "Molecular cloning and characterization of a cDNA for a novel phorbol-12-myristate-13-acetate-responsive gene that is highly expressed in an adult T-cell leukemia cell line". J Virol. 64 (10): 4632–9.
[2] Jansson AK, Emterling AM, Arbman G, Sun XF (July 2003). "Noxa in colorectal cancer: a study on DNA, mRNA and protein expression". Oncogene. 22 (30): 4675–8.
[3] Oda E, Ohki R, Murasawa H, Nemoto J, Shibue T, Yamashita T, Tokino T, Taniguchi T, Tanaka N (May 2000). "Noxa, a BH3-only member of the Bcl-2 family and candidate mediator of p53-induced apoptosis". Science. 288 (5468): 1053–1058.
[4] Hyunhee Do, Dain Kim et, al. TFAP2C increases cell proliferation by downregulating GADD45B and PMAIP1 in non-small cell lung cancer cells [J]. Biological Research volume 52, Article number: 35 (2019).

icon of phone
Call us
301-363-4651 (Available 9 a.m. to 5 p.m. CST from Monday to Friday)
icon of address
Address
7505 Fannin St., Ste 610, Room 7 (CUBIO Innovation Center), Houston, TX 77054, USA
icon of social media
Join us with

Subscribe newsletter

Leave a message

* To protect against spam, please pass the CAPTCHA test below.
CAPTCHA verification
© 2007-2024 CUSABIO TECHNOLOGY LLC All rights reserved. 鄂ICP备15011166号-1