추천 제품
분석
≥98.0% (TLC)
형태
powder or crystals
mp
223 °C (lit.)
solubility
DMF: soluble
DMSO: soluble
alcohols: soluble
형광
λex 500 nm; λem 593 nm in 0.1 M phosphate pH 8.0 (chymotrypsin)
λex 540 nm; λem 590 nm in DMSO
λex 571 nm; λem 584 nm (Reaction product)
적합성
suitable for fluorescence
저장 온도
2-8°C
SMILES string
CC(=O)Oc1ccc2N=C3C=CC(=O)C=C3Oc2c1
InChI
1S/C14H9NO4/c1-8(16)18-10-3-5-12-14(7-10)19-13-6-9(17)2-4-11(13)15-12/h2-7H,1H3
InChI key
UJWKHDKBOVPINX-UHFFFAOYSA-N
유사한 제품을 찾으십니까? 방문 제품 비교 안내
애플리케이션
suitable as fluorogenic substrate for hydrolytic enzymes (cellulases, chymotrypsin)
기타 정보
Studies on the esterase activity of cytosolic aldehyde dehydrogenase
신호어
Warning
유해 및 위험 성명서
Hazard Classifications
Acute Tox. 4 Oral - Eye Irrit. 2 - Skin Irrit. 2
Storage Class Code
11 - Combustible Solids
WGK
WGK 3
Flash Point (°F)
Not applicable
Flash Point (°C)
Not applicable
개인 보호 장비
dust mask type N95 (US), Eyeshields, Gloves
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.
이미 열람한 고객
Organic letters, 12(7), 1468-1471 (2010-03-13)
The acetate derivatives of fluorescein and resorufin exhibited a prominent turn-on type signaling behavior toward BO(3)(-) ions over other common anions. Signaling is based on the selective deprotection of acetate groups by perborate, which resulted in significant chromogenic and fluorogenic
The action of cytosolic aldehyde dehydrogenase on resorufin acetate.
Advances in experimental medicine and biology, 414, 201-208 (1997-01-01)
Biochimica et biophysica acta, 1385(1), 43-52 (1998-06-19)
Resorufin bromoacetate is a substrate that is rapidly hydrolysed by chymotrypsin. The reaction shows a pre-steady-state burst phase that may be observed by stopped flow spectrophotometry if precautions are taken against spontaneous hydrolysis of the substrate. The strongly activating effect
The Biochemical journal, 322 ( Pt 3), 701-708 (1997-03-15)
Resorufin acetate is a very good substrate for sheep liver cytosolic aldehyde dehydrogenase, both from the point of view of practical spectrophotometry and in terms of information provided about the nature of the catalysis shown by this enzyme. p-Nitrophenyl (PNP)
Chembiochem : a European journal of chemical biology, 18(13), 1204-1215 (2017-02-22)
This report describes the metabolic glycoengineering (MGE) of intracellular esterase activity in human colon cancer (LS174T) and Chinese hamster ovary (CHO) cells. In silico analysis of carboxylesterases CES1 and CES2 suggested that these enzymes are modified with sialylated N-glycans, which
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