human origin의 TBC1D19에서 에 가까운129-161의 아미노산사이에 위치한 항원결정부와 특정결합합니다.
TBC1D19 항체 (E-6)는 WB, IP, IF, IHC(P) and ELISA으로mouse, rat, human and avian유래의 TBC1D19 를 감지하는 데에 추천한다 ; 이외에, equine, canine, bovine, porcine and avian등 species와 반응할수 있습니다
IP를 위해 agarose ;WB, IHC(P) and ELISA를 위해 HRP ;또는 IF, IHC(P) and FCM를 위해 phycoerythrin or FITC 에 결합된 Anti-TBC1D19 항체 (E-6)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-IgGκ BP-HRP (mouse IgGκ binding protein-HRP) is the preferred secondary detection reagent for TBC1D19 Antibody (E-6) for WB and IHC(P) applications. This reagent is now offered in a bundle with TBC1D19 Antibody (E-6) (see ordering information below). For additional m-IgGκ BP conjugates see our complete list of Mouse IgG Binding Proteins.
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Ships via FedEx Ground to Contiguous US, Alaska, Canada, Monday through Friday. This method is used for less temperature sensitive items such as lab ware and animal
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TBC1D19 Antibody (E-6) is a high quality monoclonal TBC1D19 antibody (also designated TBC1D19 antibody) suitable for the detection of the TBC1D19 protein of mouse, rat and human origin. TBC1D19 Antibody (E-6) is available as both the non-conjugated anti-TBC1D19 antibody form, as well as multiple conjugated forms of anti-TBC1D19 antibody, including agarose, HRP, PE, FITC and multiple Alexa Fluor® conjugates. TBC1D19 (TBC1 domain family member 19) is a 526 amino acid protein that contains one Rab-GAP TBC domain and may act as a GTPase-activating protein for Rab family proteins. The gene that encodes TBC1D19 contains 178,915 bases and maps to human chromosome 4p15.2. Chromosome 4 represents approximately 6% of the human genome and contains nearly 900 genes. Notably, the Huntingtin gene, which is found to encode an expanded glutamine tract in cases of Huntington′s disease, is on chromosome 4. FGFR-3 is also encoded by a gene located on chromosome 4 and has been associated with thanatophoric dwarfism, achondroplasia, Muenke syndrome and bladder cancer. Chromosome 4 is tied to Ellis-van Creveld syndrome, methylmalonic acidemia and polycystic kidney disease.
For Research Use Only. Not Intended for Diagnostic or Therapeutic Use.
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