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Merck
모든 사진(2)

주요 문서

H6268

Sigma-Aldrich

Hide–Remazol Brilliant Blue R

protease substrate, powder

동의어(들):

Hide powder azure, Remazol Brilliant Blue R–Hide

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모든 사진(2)

About This Item

CAS Number:
37340-54-8
Beilstein:
5629635
MDL number:
MFCD00131326
UNSPSC 코드:
12352204
NACRES:
NA.32

product name

Hide–Remazol Brilliant Blue R, protease substrate

Quality Level

200

형태

powder

저장 온도

2-8°C

유사한 제품을 찾으십니까? 방문 제품 비교 안내

애플리케이션

Hide−Remazol Brilliant Blue R has been used:
  • to study the substrate specificity of a purified collagenase preparation from Clostridium histolyticum
  • to mix with cytotoxic samples for hide powder azure protease activity assay
  • as a high molecular weight substrate to test the inhibition of trypsin by the purified recombinant rat bikunin, α1-m/bikunin precursor, and α1-m
  • as a substrate to obtain the inhibition of snake venom protease activity by the addition of exogenous citrate

기타 정보

Hide powder covalently linked to Remazol Brilliant Blue R

기질

Chromogenic substrate for trypsin

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)

시험 성적서(COA)

제품의 로트/배치 번호를 입력하여 시험 성적서(COA)을 검색하십시오. 로트 및 배치 번호는 제품 라벨에 있는 ‘로트’ 또는 ‘배치’라는 용어 뒤에서 찾을 수 있습니다.

이 제품을 이미 가지고 계십니까?

문서 라이브러리에서 최근에 구매한 제품에 대한 문서를 찾아보세요.

문서 라이브러리 방문

Citrate inhibition of snake venom proteases
Odell G V, et al.
Toxicon, 36(12), 1801-1806 (1998)
Expression of a functional proteinase inhibitor capable of accepting xylose: bikunin
Falkenberg C, et al.
Archives of Biochemistry and Biophysics, 387(1), 99-106 (2001)
Soluble, dye-labelled substrates for a micro-plate assay of proteinase activity
Wolf G A and Wirth S J
Journal of Microbiological Methods, 25(3), 337-342 (1996)
J Melrose et al.
Archives of orthopaedic and trauma surgery, 114(3), 145-152 (1995-01-01)
Chemonucleolysis is a therapeutic procedure whereby a degradative enzyme is injected intradiscally to reduce disc height/width by depolymerisation of extracellular matrix components. This process is considered to diminish disc pressure on inflamed nerve roots, resulting in the alleviation of sciatic
S Mischke
Microbios, 87(352), 175-183 (1996-01-01)
Four chromogenic substrates were compared, and methods were developed for measuring protease activity from fungi. Digestion of azoalbumin, a water-soluble substrate, resulted in dye release most closely proportional to enzyme activity. Substrates insoluble in water were advantageous for time-course studies
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