추천 제품
제품명
Ponceau BS, Dye content ≥55 %
양식
powder
Quality Level
구성
Dye content, ≥55%
기술
microbe id | staining: suitable
색상
red to brown
solubility
ethanol: 1 mg/mL
H2O: >30 mg/mL
εmax
≥19000 at 510 nm
응용 분야
diagnostic assay manufacturing
hematology
histology
저장 온도
room temp
SMILES string
[Na+].[Na+].Oc1ccc2ccccc2c1\N=N\c3ccc(cc3S([O-])(=O)=O)\N=N\c4ccc(cc4)S([O-])(=O)=O
InChI
1S/C22H16N4O7S2.2Na/c27-20-12-5-14-3-1-2-4-18(14)22(20)26-25-19-11-8-16(13-21(19)35(31,32)33)24-23-15-6-9-17(10-7-15)34(28,29)30;;/h1-13,27H,(H,28,29,30)(H,31,32,33);;/q;2*+1/p-2/b24-23+,26-25+;;
InChI key
VVAVKBBTPWYADW-RVTJCSDESA-L
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애플리케이션
Ponceau BS has been used in Masson′s trichrome stain for the staining of collagen. It has also been used for eosinophil staining.
생화학적/생리학적 작용
Ponceau BS is used in Masson′s trichrome staining procedure, along with acid fuchsin, for the labeling of collagen and muscle red.
Storage Class Code
11 - Combustible Solids
WGK
WGK 3
Flash Point (°F)
Not applicable
Flash Point (°C)
Not applicable
개인 보호 장비
Eyeshields, Gloves, type N95 (US)
이미 열람한 고객
Principles & Interpretation of Laboratory Practices in Surgical Pathology (2016)
Interleukin-4 has basophilic and eosinophilic cell growth-promoting activity on cord blood cells.
Blood, 75, 67-67 (1990)
Amino acids, 36(2), 251-260 (2008-03-28)
We studied the non-specific interactions of two azo compounds: biebrich scarlet (BS) and naphthochrome green (NG), with four model proteins: bovine serum albumin, ovalbumin, poly-L-lysine and hemoglobin by UV-VIS spectrometry, fluorophotometry and circular dichroism melting technique. The optimal acidities of
Development of a bone reconstruction technique using a solid free-form fabrication (SFF)-based drug releasing scaffold and adipose-derived stem cells.
Journal of Biomedical Materials Research Part A, 101, 1865-1865 (2013)
The journal of histochemistry and cytochemistry : official journal of the Histochemistry Society, 51(2), 253-257 (2003-01-21)
Here we describe a simple histochemical technique that provides an improved approach to identifying eosinophil components in tissues through the formation of photoreactive complexes that produce stable fluorescent emissions. This method worked readily with histological tissue sections 6-60 microm thick
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