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Merck

C3535

Complement C8 from human serum

suitable for radioiodination, RIA, ≥85% (SDS-PAGE), ≥125,000 C8H50 units/mg protein (using C8 deficient serum)

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크기 선택

0.1 MG
₩561,904

₩561,904


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제품정보 (DICE 배송 시 비용 별도)

CAS 번호:
MDL number:
UNSPSC 코드:
12352202
NACRES:
NA.61

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기술 서비스
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도움 문의

생물학적 소스

human

Quality Level

분석

≥85% (SDS-PAGE)

양식

solution

특이 활성도

≥125,000 C8H50 units/mg protein (using C8 deficient serum)

농도

1 mg/mL in PBS, pH 7.2

기술

immunoelectrophoresis: suitable

적합성

suitable for radioiodination, RIA

UniProt 수납 번호

배송 상태

dry ice

저장 온도

−70°C

유전자 정보

human ... C8A(731)

유사한 품목 비교

전체 비교 보기

차이점 표시

1 of 4

이 품목
C3660C2910C3160
assay

≥85% (SDS-PAGE)

assay

≥85% (SDS-GE)

assay

≥85% (SDS-GE)

assay

≥90% (SDS-PAGE)

technique(s)

immunoelectrophoresis: suitable

technique(s)

-

technique(s)

activity assay: suitable

technique(s)

activity assay: suitable

biological source

human

biological source

human

biological source

human

biological source

human serum

concentration

1 mg/mL in PBS, pH 7.2

concentration

-

concentration

-

concentration

1 mg/mL in PBS, pH 7.2

suitability

suitable for radioiodination, RIA

suitability

-

suitability

-

suitability

-

form

solution

form

solution

form

solution

form

solution

애플리케이션

Complement C8 is one of the end terminals of the complement system contained in the membrane attack complex (MAC). In the (MAC), C8 initiates and coordinates MAC pore formation. It has been used in research to investigate the mechanisms of how C8-C9 and C9-C9 interactions facilitate folding of the membrane attack complex perforin (MACPF) domain to form the circular pore.

생화학적/생리학적 작용

C8 is one of the components of the terminal complement complex and is required for a functional complement system. It is composed of disulfide-linked C8α and C8γ and a noncovalently associated C8β chain. During formation of the membrane-attack complex, a domain on C8α induces C9 to polymerize and form a pore-like structure.

분석 메모

Functionally pure by a sensitive hemolytic assay using depleted sera.

기타 정보

면책조항

RESEARCH USE ONLY. This product is regulated in France when intended to be used for scientific purposes, including for import and export activities (Article L 1211-1 paragraph 2 of the Public Health Code). The purchaser (i.e. enduser) is required to obtain an import authorization from the France Ministry of Research referred in the Article L1245-5-1 II. of Public Health Code. By ordering this product, you are confirming that you have obtained the proper import authorization.

Storage Class Code

10 - Combustible liquids

WGK

WGK 3

Flash Point (°F)

Not applicable

Flash Point (°C)

Not applicable


가장 최신 버전 중 하나를 선택하세요:

시험 성적서(COA)

Lot/Batch Number

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문서 라이브러리에서 최근에 구매한 제품에 대한 문서를 찾아보세요.

문서 라이브러리 방문

Daniel J Slade et al.
Biochemistry, 45(16), 5290-5296 (2006-04-19)
Human C8 is one of five components of the membrane attack complex of complement (MAC). It contains three subunits (C8alpha, C8beta, C8gamma) arranged as a disulfide-linked C8alpha-gamma dimer that is noncovalently associated with C8beta. C8alpha, C8beta, and complement components C6
Leslie L Lovelace et al.
The Journal of biological chemistry, 286(20), 17585-17592 (2011-04-02)
C8 is one of five complement proteins that assemble on bacterial membranes to form the lethal pore-like "membrane attack complex" (MAC) of complement. The MAC consists of one C5b, C6, C7, and C8 and 12-18 molecules of C9. C8 is
Doryen Bubeck et al.
Journal of molecular biology, 405(2), 325-330 (2010-11-16)
Complement component C8 plays a pivotal role in the formation of the membrane attack complex (MAC), an important antibacterial immune effector. C8 initiates membrane penetration and coordinates MAC pore formation. High-resolution structures of C8 subunits have provided some insight into
Zhexu Chi et al.
Molecular cell, 80(1), 43-58 (2020-09-17)
Immune cell function depends on specific metabolic programs dictated by mitochondria, including nutrient oxidation, macromolecule synthesis, and post-translational modifications. Mitochondrial adaptations have been linked to acute and chronic inflammation, but the metabolic cues and precise mechanisms remain unclear. Here we

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