|Immunohistochemistry (Paraffin) (IHC (P))||1:100|
|Tested Species reactivity||Human, Mouse|
|Host / Isotype||Rabbit / IgG|
|Immunogen||Synthetic peptide corresponding to the C-terminal region of the human protein.|
|Purification||Antigen affinity chromatography|
|Storage buffer||PBS, pH 7.4, with 1% BSA|
|Contains||0.09% sodium azide|
|Storage conditions||4° C, do not freeze|
PA1-21004 detects APC in Human and Mouse samples.
PA1-21004 has been successfully used in Immunohistochemistry (Paraffin) procedures.
PA1-21004 immunogen corresponds to Synthetic peptide corresponding to the C-terminal region of the human protein. .
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.
For Research Use Only. Not for use in diagnostic procedures. Not for resale without express authorization.
Protein Aliases: adenomatosis polyposis coli tumor suppressor; Adenomatous Polyposis Coli; Adenomatous polyposis coli protein; APC; Deleted in polyposis 2.5; DP2; DP2.5; DP3; FPC; multiple intestinal neoplasia; Protein APC; protein phosphatase 1, regulatory subunit 46; truncated adenomatosis polyposis coli; WNT signaling pathway regulator
Gene Aliases: AI047805; APC; AU020952; AW124434; BTPS2; CC1; DP2; DP2.5; DP3; GS; mAPC; Min; PPP1R46
UniProt ID: (Human) P25054
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