catalog number :
MBS8245445
products full name :
Anti-Axin-2 Antibody
products short name :
[Axin-2]
products name syn :
[Axin-2; Axin-like protein; Axil; Axis inhibition protein 2; Conductin]
other names :
[axin-2; Axin-2; axin-2; axin 2; Axin-like protein; Axil; Axis inhibition protein 2; Conductin]
products gene name :
[AXIN2]
other gene names :
[AXIN2; AXIN2; AXIL; ODCRCS; Axil]
uniprot entry name :
AXIN2_HUMAN
reactivity :
Human, Mouse, Rat
specificity :
Recognizes endogenous levels of Axin-2 protein.
purity :
The antibody was purified by immunogen affinity chromatography.
form :
Liquid in 0.42% Potassium phosphate, 0.87% Sodium chloride, pH 7.3, 30% glycerol, and 0.01% sodium azide.
storage stability :
Shipped at 4 degree C. Upon delivery aliquot and store at -20 degree C for one year. Avoid freeze/thaw cycles.
tested application :
Western Blot (WB), Immunofluorescence (IF), Immunocytochemistry (ICC)
app notes :
WB: 1/500 - 1/2000; IF/ICC: 1/50 - 1/200
image1 heading :
Western Blot (WB)
image2 heading :
Immunofluorescence (IF)
other info1 :
Source: Rabbit. Immunogen: Recombinant full length protein of human Axin-2
products description :
Rabbit polyclonal antibody to Axin-2
ncbi acc num :
NP_004646.3
ncbi gb acc num :
NM_004655.3
ncbi mol weight :
93,558 Da
ncbi pathways :
Basal Cell Carcinoma Pathway (83113); Basal Cell Carcinoma Pathway (525); Binding Of TCF/LEF:CTNNB1 To Target Gene Promoters Pathway (1269603); Canonical Wnt Signaling Pathway (138032); Colorectal Cancer Pathway (83106); Colorectal Cancer Pathway (518); Degradation Of AXIN Pathway (1269606); Endometrial Cancer Pathway (83109); Endometrial Cancer Pathway (521); Formation Of The Beta-catenin:TCF Transactivating Complex Pathway (1269602)
ncbi summary :
The Axin-related protein, Axin2, presumably plays an important role in the regulation of the stability of beta-catenin in the Wnt signaling pathway, like its rodent homologs, mouse conductin/rat axil. In mouse, conductin organizes a multiprotein complex of APC (adenomatous polyposis of the colon), beta-catenin, glycogen synthase kinase 3-beta, and conductin, which leads to the degradation of beta-catenin. Apparently, the deregulation of beta-catenin is an important event in the genesis of a number of malignancies. The AXIN2 gene has been mapped to 17q23-q24, a region that shows frequent loss of heterozygosity in breast cancer, neuroblastoma, and other tumors. Mutations in this gene have been associated with colorectal cancer with defective mismatch repair. [provided by RefSeq, Jul 2008]
uniprot summary :
axin 2: is a negative regulator of the Wnt pathway, which is critical in stem cell signaling, morphogenesis, the mesenchymal-epithelial transition, and many cancers. Axin functions as a tumor suppressor. Probably facilitates the phosphorylation of beta-catenin and APC by GSK3B, leading to their ubiquitination and subsequent proteolysis. Is downregulated during progression of esophageal squamous cell carcinoma. Axin1/2 mediate cross-talk between TGF-beta and Wnt signaling pathways. Protein type: Adaptor/scaffold. Chromosomal Location of Human Ortholog: 17q24.1. Cellular Component: beta-catenin destruction complex; cell cortex; centrosome; cytoplasm; cytoplasmic membrane-bound vesicle; cytoplasmic microtubule; cytosol; Golgi apparatus; microtubule cytoskeleton; nucleoplasm; nucleus; plasma membrane; postsynaptic density. Molecular Function: beta-catenin binding; enzyme binding; GTPase activator activity; protein binding; protein kinase binding; ubiquitin protein ligase binding. Biological Process: bone mineralization; cell proliferation; dorsal/ventral axis specification; intramembranous ossification; maintenance of DNA repeat elements; mRNA stabilization; negative regulation of cell proliferation; negative regulation of osteoblast differentiation; odontogenesis; positive regulation of GTPase activity; positive regulation of protein amino acid phosphorylation; regulation of mismatch repair; regulation of transcription, DNA-dependent; Wnt receptor signaling pathway. Disease: Oligodontia-colorectal Cancer Syndrome