아미노 산1119-1168 mapping near the C-terminus of WWC2 of human 의하고 기원한다
안티-WWC2 항체 (H-1)는 WB, IP, IF and ELISA으로 mouse, rat and human유래의 WWC2 를 감지하는 데에 추천한다.
IP를 위해 agarose ;WB, IHC(P) and ELISA를 위해 HRP ;또는 IF, IHC(P) and FCM를 위해 phycoerythrin or FITC 에 결합된 Anti-WWC2 항체 (H-1)를 제공한다.
WB (RGB), IF, IHC(P) 와FCM, RGB fluorescent imaging systems, such as iBright™ FL1000, FluorChem™, Typhoon, Azure and other comparable systems에 사용가능한 Alexa Fluor® 488, Alexa Fluor® 546, Alexa Fluor® 594 or Alexa Fluor® 647결합제품도 있습니다.
WB (NIR), IF와FCM,Near-Infrared (NIR) detection systems, such as LI-COR®Odyssey®, iBright™ FL1000, FluorChem™, Typhoon, Azure and other comparable systems에 사용가능한 Alexa Fluor® 680 or Alexa Fluor® 790 결합제품도 있습니다.
m-IgG2b BP-HRP and m-IgGκ BP-HRP are the preferred secondary detection reagents for WWC2 Antibody (H-1) for WB applications. These reagents are now offered in bundles with WWC2 Antibody (H-1) (see ordering information below).
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WWC2 Antibody (H-1) is a high quality monoclonal WWC2 antibody (also designated WWC2 antibody) suitable for the detection of the WWC2 protein of mouse, rat and human origin. WWC2 Antibody (H-1) is available as both the non-conjugated anti-WWC2 antibody form, as well as multiple conjugated forms of anti-WWC2 antibody, including agarose, HRP, PE, FITC and multiple Alexa Fluor® conjugates. WWC2 (WW and C2 domain containing 2), also known as BOMB (BH-3-only member B), is a 1,192 amino acid protein belonging to the WWC family. Containing one C2 domain and two WW domains, WWC2 exists as seven alternatively spliced isoforms and is encoded by a gene located on human chromosome 4q35.1. Representing approximately 6% of the human genome, chromosome 4 contains nearly 900 genes. Notably, the Huntingtin gene, which is found to encode an expanded glutamine tract in cases of Huntington′s disease, located on chromosome 4. FGFR-3 is also encodedby a gene that maps to chromosome 4 and has been associated with thanatophoric dwarfism, achondroplasia, Muenke syndrome and bladder cancer. Chromosome 4 is also tied to Ellis-van Creveld syndrome, methylmalonic acidemia and polycystic kidney disease. Chromosome 4 reportedly contains the largest gene deserts (regions of the genome with no protein encoding genes) and has one of the two lowest recombination frequencies of the human chromosomes.
For Research Use Only. Not Intended for Diagnostic or Therapeutic Use.
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