Comparison

gamma Catenin

Item no. 18-272-196270
Manufacturer GENWAY
Amount 0.5 ml
Category
Type Antibody
Applications WB, IP, IHC
Specific against other
ECLASS 10.1 32160702
ECLASS 11.0 32160702
UNSPSC 12352203
Alias GWB-77AF70
Similar products 18-272-196270
Available
Genway ID:
GWB-77AF70
Isotype:
IgG
Immunogen:
Synthetic peptide (Human) (C terminal).
Antigen Species:
Human
Positive Control:
Breast carcinoma
Target:
gamma Catenin
Localization:
Cytoplasmic
Concentration:
0. 2 mg/ml Storage
Buffer:
Phosphate-buffered saline pH 7. 4 containing 1% BSA and 0. 09% sodium azide
Application Note:
IHC-P: Use at a dilution of 1/100 for 10 minutes at RT. Staining of formalin fixed tissues requires boiling tissue sections in 10mM citrate buffer pH 6. 0 for 10 mins followed by cooling at RT for 20 min. Ab 15153 stains gamma catenin on the cell membrane and in the cytoplasm of breast carcinoma. IP: Use at an assay dependent dilution. WB: Use at an assay dependent dilution. Predicted
Molecular Weight:
82 kDa. Not tested in other applications. Optimal dilutions/concentrations should be determined by the end user. Cellular
Localization:
Cytoplasmic Gamma Catenin is a common junctional plaque protein. The membrane-associated plaques are architectural elements in an important strategic position to influence the arrangement and function of both the cytoskeleton and the cells within the tissue. The presence of gamma Catenin in both the desmosomes and in the intermediate junctions suggests that it plays a central role in the structure and function of submembranous plaques.
Function:
Common junctional plaque protein. The membrane-associated plaques are architectural elements in an important strategic position to influence the arrangement and function of both the cytoskeleton and the cells within the tissue. The presence of plakoglobin in both the desmosomes and in the intermediate junctions suggests that it plays a central role in the structure and function of submembranous plaques.
Subunit:
Homodimer. Interacts with MUC1.
Subcellular Location:
Cell junction adherens junction. Cell junction desmosome. Cytoplasm cytoskeleton. Membrane; Peripheral membrane protein. Note=Cytoplasmic in a soluble and membrane-associated form.
Disease:
Defects in JUP are the cause of Naxos disease (NXD) [MIM:601214]. NXD is an autosomal recessive disorder combining diffuse non-epidermolytic palmoplantar keratoderma with arrhythmogenic right ventricular dysplasia/cardiomyopathy and woolly hair.
Disease:
Defects in JUP are the cause of familial arrhythmogenic right ventricular dysplasia type 12 (ARVD12) [MIM:611528]; also called arrhythmogenic right ventricular cardiomyopathy type 12 (ARVC12). ARVD is an autosomal dominant disease characterized by partial degeneration of the myocardium of the right ventricle electrical instability and sudden death. It is clinically defined by electrocardiographic and angiographic criteria; pathologic findings replacement of ventricular myocardium with fatty and fibrous elements preferentially involve the right ventricular free wall.
Similarity:
Belongs to the beta-catenin family.
Similarity:
Contains 9 ARM repeats.

Note: The presented information and documents (Manual, Product Datasheet, Safety Datasheet and Certificate of Analysis) correspond to our latest update and should serve for orientational purpose only. We do not guarantee the topicality. We would kindly ask you to make a request for specific requirements, if necessary.

All products are intended for research use only (RUO). Not for human, veterinary or therapeutic use.

Amount: 0.5 ml
Available: In stock
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