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0512-67156496
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商品描述
β-Catenin (phospho-Ser675) rabbit pAb
- Catalog No.:YP1558
- Applications:WB
- Reactivity:Human,Mouse,Rat
- Data Sheet
- MSDS
- Support
- Description
- References ( 0 )
- Protocol
- Gene Name:
- CTNNB1 CTNNB OK/SW-cl.35 PRO2286
- Protein Name:
- β-Catenin (Ser675)
- Human Gene Id:
- 1499
- Human Swiss Prot No:
- P35222
- Mouse Gene Id:
- 12387
- Mouse Swiss Prot No:
- Q02248
- Rat Gene Id:
- 84353
- Rat Swiss Prot No:
- Q9WU82
- Immunogen:
- Synthesized phosho peptide around human β-Catenin (Ser675)
- Specificity:
- This antibody detects endogenous levels ofHuman Mouse Rat β-Catenin (phospho-Ser675)
- Formulation:
- Liquid in PBS containing 50% glycerol, 0.5% BSA and 0.02% sodium azide.
- Source:
- Rabbit
- Dilution:
- WB 1:1000-2000
- Purification:
- The antibody was affinity-purified from rabbit serum by affinity-chromatography using specific immunogen.
- Concentration:
- 1 mg/ml
- Storage Stability:
- -20°C/1 year
- Other Name:
- Catenin beta-1 (Beta-catenin)
- Observed Band(KD):
- 100
- Background:
- catenin beta 1(CTNNB1)Homo sapiensThe protein encoded by this gene is part of a complex of proteins that constitute adherens junctions (AJs). AJs are necessary for the creation and maintenance of epithelial cell layers by regulating cell growth and adhesion between cells. The encoded protein also anchors the actin cytoskeleton and may be responsible for transmitting the contact inhibition signal that causes cells to stop dividing once the epithelial sheet is complete. Finally, this protein binds to the product of the APC gene, which is mutated in adenomatous polyposis of the colon. Mutations in this gene are a cause of colorectal cancer (CRC), pilomatrixoma (PTR), medulloblastoma (MDB), and ovarian cancer. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Aug 2016],
- Function:
- disease:A chromosomal rearrangement involving CTNNB1 may be a cause of salivary gland pleiomorphic adenomas (PA) [181030]. Pleiomorphic adenomas are the most common benign epithelial tumors of the salivary gland. Translocation t(3;8)(p21;q12) with PLAG1.,disease:Activating mutations in CTNNB1 have oncogenic activity resulting in tumor development. Somatic mutations are found in various tumor types, including colon cancers, ovarian and prostate carcinomas, hepatoblastoma (HB), hepatocellular carcinoma (HCC). HBs are malignant embryonal tumors mainly affecting young children in the first three years of life.,disease:Defects in CTNNB1 are a cause of medulloblastoma (MDB) [MIM:155255]. MDB is a malignant, invasive embryonal tumor of the cerebellum with a preferential manifestation in children.,disease:Defects in CTNNB1 are a cause of pilomatrixoma (PTR) [MIM:132600]; a common benign skin tum
- Subcellular Location:
- spindle pole,nucleus,nucleoplasm,transcription factor complex,nuclear euchromatin,cytoplasm,centrosome,cytosol,plasma membrane,cell-cell junction,adherens junction,cell-cell adherens junction,fascia adherens,bicell
- Expression:
- Brain,Colon adenocarcinoma,Epithelium,Fetal liver,Placenta,Skin,
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