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APC Antibody (Center) Blocking Peptide

Synthetic peptide

Product Information
Primary Accession P25054
Clone Names 110729003
Peptide ID 110729003
Additional Information
Gene ID 324
Other Names Adenomatous polyposis coli protein, Protein APC, Deleted in polyposis 25, APC, DP25
Format Synthetic peptide was lyophilized with 100% acetonitrile and is supplied as a powder. Reconstitute with 0.1 ml DI water for a final concentration of 1 mg/ml.
StorageMaintain refrigerated at 2-8°C for up to 6 months. For long term storage store at -20°C.
PrecautionsThis product is for research use only. Not for use in diagnostic or therapeutic procedures.
Protein Information
Name APC
Synonyms DP2.5
Function Tumor suppressor. Promotes rapid degradation of CTNNB1 and participates in Wnt signaling as a negative regulator. APC activity is correlated with its phosphorylation state. Activates the GEF activity of SPATA13 and ARHGEF4. Plays a role in hepatocyte growth factor (HGF)-induced cell migration. Required for MMP9 up-regulation via the JNK signaling pathway in colorectal tumor cells. Acts as a mediator of ERBB2-dependent stabilization of microtubules at the cell cortex. It is required for the localization of MACF1 to the cell membrane and this localization of MACF1 is critical for its function in microtubule stabilization.
Cellular Location Cell junction, adherens junction. Cytoplasm, cytoskeleton. Cell projection, lamellipodium. Cell projection, ruffle membrane. Cytoplasm. Cell membrane. Note=Associated with the microtubule network at the growing distal tip of microtubules Accumulates in the lamellipodium and ruffle membrane in response to hepatocyte growth factor (HGF) treatment. The MEMO1-RHOA-DIAPH1 signaling pathway controls localization of the phosophorylated form to the cell membrane
Tissue Location Expressed in a variety of tissues.
Research Areas
Citations (0)

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This gene encodes a tumor suppressor protein that acts asan antagonist of the Wnt signaling pathway. It is also involved inother processes including cell migration and adhesion,transcriptional activation, and apoptosis. Defects in this genecause familial adenomatous polyposis (FAP), an autosomal dominantpre-malignant disease that usually progresses to malignancy.Disease-associated mutations tend to be clustered in a small regiondesignated the mutation cluster region (MCR) and result in atruncated protein product.


Chung, K.H., et al. J Neurosurg Pediatr 6(4):372-376(2010)Rai, K., et al. Cell 142(6):930-942(2010)Poulogiannis, G., et al. Proc. Natl. Acad. Sci. U.S.A. 107(34):15145-15150(2010)Jaulin, F., et al. J. Cell Biol. 190(3):443-460(2010)Sugiyama, N., et al. Mol. Cell Proteomics 6(6):1103-1109(2007)

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$ 80.00
Cat# BP19274c
(40 western blots)
Availability: In Stock
Bulk Size
Seasonal Special on Bulk Order
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