추천 제품
Quality Level
분석
≥97.5%
품질
for spectrophotometric det. of Se
기술
UV/Vis spectroscopy: suitable
SMILES string
O.Cl.Cl.Cl.Cl.Nc1ccc(cc1N)-c2ccc(N)c(N)c2
InChI
1S/C12H14N4.4ClH.H2O/c13-9-3-1-7(5-11(9)15)8-2-4-10(14)12(16)6-8;;;;;/h1-6H,13-16H2;4*1H;1H2
InChI key
DXWSCXIZIHILNP-UHFFFAOYSA-N
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일반 설명
3,3′-diaminobenzidine-tetrahydrochloride-dihydrate (DAB) is toxic in nature, and is one of the most potent marker being used in immunochemistry, mostly at the electron and light microscope levels.
애플리케이션
3,3′-diaminobenzidine-tetrahydrochloride-dihydrate (DAB) was used as a chromogen, for detecting the antigen-antibody complex.
기타 정보
Reagent for the spectrophotometric determination of selenium; Peroxidase stain. Differentiation between two classes of mycobacterial catalase in polyacrylamide electrophoresis gels; Specific indication of hemoproteins in polyacrylamide gels by double staining
신호어
Danger
유해 및 위험 성명서
Hazard Classifications
Acute Tox. 4 Oral - Carc. 1B - Eye Irrit. 2 - Muta. 2
Storage Class Code
6.1C - Combustible acute toxic Cat.3 / toxic compounds or compounds which causing chronic effects
WGK
WGK 3
Flash Point (°F)
Not applicable
Flash Point (°C)
Not applicable
개인 보호 장비
Eyeshields, Gloves, type N95 (US)
이미 열람한 고객
HistoGreen: a new alternative to 3, 3'-diaminobenzidine-tetrahydrochloride-dihydrate (DAB) as a peroxidase substrate in immunohistochemistry"
Brain Research, 14 (2), 107-118 (2005)
Interleukin-8 in the Human Endometrium 1.
J. Clin. Endocr., 83 (5), 1783-1787 (1998)
Analytical Chemistry, 30, 1370-1370 (1958)
Analytical biochemistry, 157(1), 89-92 (1986-08-15)
Mycobacteria produce two classes of catalase, designated T and M. Only the T-catalase also has a peroxidase-like function. When a 3,3'-diaminobenzidine (DAB) peroxidase stain was applied to polyacrylamide gel electrophoresis gels, followed by a ferricyanide negative stain for catalase, isoenzymes
Analytical biochemistry, 136(2), 509-514 (1984-02-01)
Hemoproteins were revealed in polyacrylamide gels in the presence of sodium dodecyl sulfate by staining with different benzidine derivatives. When the protein samples were treated with either beta-mercaptoethanol or dithiothreitol, a significant decrease in peroxidase activity of the proteins possessing
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