immunoblotting: 3-6 μg/mL using lysates of HeLa or SW620 cells. immunohistochemistry: 10-20 μg/mL using formalin-fixed, paraffin-embedded human colon or duodenum. indirect immunofluorescence: 2-4 μg/mL using Caco-2 cells.
immunoblotting: 3-6 μg/mL using lysates of HeLa or SW620 cells. immunohistochemistry: 10-20 μg/mL using formalin-fixed, paraffin-embedded human colon or duodenum. indirect immunofluorescence: 2-4 μg/mL using Caco-2 cells.
Adenomatous Polyposis Coli (APC) is a tumor suppressor gene. The APC gene encodes a large multifunctional protein that has critical functions in cell migration, adhesion and proliferation. It is a shuttling nucleo-cytoplasmic protein expressed in various tissues and its expression in the colorectal epithelium contributes to its normal growth and differentiation.
免疫原
synthetic peptide corresponding to a sequence at the C-terminal region of human APC, conjugated to KLH. The corresponding sequence is identical in human APC isoform b and highly conserved (single amino acid substitution) in rat and mouse APC.
應用
Anti-APC (C-terminal) antibody produced in rabbit has been used in:
immunoblotting
immunofluorescence
immunohistochemistry
生化/生理作用
Adenomatous Polyposis Coli (APC) has a key role in the proteasome-mediated degradation of β-catenin. APC mutations cause accumulation of β-catenin in the nucleus leading to activation of LEF-1 and/or TCF, and the induction of target genes such as the oncogene c-myc. It is involved in regulation of mitotic chromosome separation and stability.
外觀
Solution in 0.01 M phosphate buffered saline, pH 7.4, containing 15 mM sodium azide.
免責聲明
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.
The molecular biological mechanisms underlying the evolutionary biologic changes leading to carcinogenesis remain unclear. The main objective of our study was to explore the evolution of the microbiota community and molecules related with CRC in the dynamic transition from normal
Adenomatous polyposis coli (APC): a multi-functional tumor suppressor gene
Aoki K and Taketo MM
Journal of Cell Science, 120(19), 3327-3335 (2007)