APC Antibody (Ali 12-28) - BSA Free

This gene encodes a tumor suppressor protein that includes among its many intracellular functions one of nuclear export. Defects in this gene cause familial adenomatous polyposis (FAP), an autosomal dominant pre-malignant disease that usually progresses to malignancy. Disease-associated mutations tend to be clustered in a small region designated the mutation cluster region (MCR) and result in a truncated protein product.

This product is for research use only and is not approved for use in humans or in clinical diagnosis. Primary Antibodies are guaranteed for 1 year from date of receipt.

We have publications tested in 1 confirmed species: Human.

We have publications tested in 2 applications: IHC-P, WB.

Showing Publications 1 - 3 of 3.

Publications using NB100-667	Applications	Species
Awadalla A, Aboelenin H, Hemmaid KZ. Pattern of DNA Hypermethylation of APC, P16, P73, P16, O 6 MMGT, CD99 and CDH1 Genes in Bladder Cancer with Hepatitis C Viral (HCV) Infection International Journal of Cancer Research 2015-08-06 (IHC-P, Human)	IHC-P	Human
Ranes M, Zaleska M, Sakalas S Et al. Reconstitution of the destruction complex defines roles of AXIN polymers and APC in beta-catenin capture, phosphorylation, and ubiquitylation Molecular cell 2021-08-19 [PMID: 34352208] (WB, Human)	WB	Human
Abutaily AS et al. Cadherins, catenins APC in pleural malignant mesothelioma. J Pathol 201:355-62. 2003-01-01 [PMID: 14595746]

Array NB100-667

• APC Antibodies
• APC Lysate
• APC Proteins