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Merck
모든 사진(1)

문서

C6607

Sigma-Aldrich

Caspase 10 human

>90% (SDS-PAGE), recombinant, expressed in E. coli, lyophilized powder, 8,000 units/mg protein (Bradford)

동의어(들):

Flice2, Mch4

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About This Item

MDL number:
UNSPSC 코드:
12352200
NACRES:
NA.32

재조합

expressed in E. coli

Quality Level

분석

>90% (SDS-PAGE)

형태

lyophilized powder

특이 활성도

8,000 units/mg protein (Bradford)

분자량

~30 kDa

solubility

PBS: soluble

UniProt 수납 번호

배송 상태

dry ice

저장 온도

−70°C

유전자 정보

human ... CASP10(843)

생화학적/생리학적 작용

Caspase 10 has two death effector domains (DEDs) that bind to the DED in the adapter molecule FADD and recruits both TNFR1 and CD95 to form complexes with these receptors. Caspase 10 cleaves and activates caspases 3, 4, 6, 7, 8 and 9 which causes the proteolytic cleavage of many key proteins such as PARP. Based on gene expression studies, caspase 10 may be crucial in embryonic development. In view of its structural homology to caspase 8, the initiator caspase in death receptor-mediated apoptosis, caspase 10 may function in a similar and redundant manner.

단위 정의

One unit will hydrolyze 1 nmol of the caspase substrate IETD-pNA to IETD and p-nitroaniline per hour at pH 7.2 at 37 °C.

물리적 형태

Lyophilized powder containing 0.052% ammonium sulfate, 0.158% Tris−HCl, and 0.76% sodium chloride.

Storage Class Code

10 - Combustible liquids

WGK

nwg

Flash Point (°F)

Not applicable

Flash Point (°C)

Not applicable


시험 성적서(COA)

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문서 라이브러리 방문

Caspases: the executioners of apoptosis.
Cohen, G.M.
Biochemistry, 326 (part 1), 1-1 (1997)
Marcin Poreba et al.
Nature protocols, 12(10), 2189-2214 (2017-09-22)
Many biologically and chemically based approaches have been developed to design highly active and selective protease substrates and probes. It is, however, difficult to find substrate sequences that are truly selective for any given protease, as different proteases can demonstrate
Marcin Poreba et al.
Nature protocols, 12(10), 2189-2214 (2017-09-22)
Many biologically and chemically based approaches have been developed to design highly active and selective protease substrates and probes. It is, however, difficult to find substrate sequences that are truly selective for any given protease, as different proteases can demonstrate

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