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Merck
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문서

MAB1628

Sigma-Aldrich

Anti-Myosin Antibody, slow muscle, clone NOQ7.5.4D

clone NOQ7.5.4D, Chemicon®, from mouse

동의어(들):

Anti-CMD1S, Anti-CMH1, Anti-MPD1, Anti-MYHCB, Anti-SPMD, Anti-SPMM

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About This Item

UNSPSC 코드:
12352203
eCl@ss:
32160702
NACRES:
NA.41

생물학적 소스

mouse

Quality Level

항체 형태

purified immunoglobulin

항체 생산 유형

primary antibodies

클론

NOQ7.5.4D, monoclonal

종 반응성

rat, feline, human

제조업체/상표

Chemicon®

기술

immunohistochemistry: suitable
radioimmunoassay: suitable
western blot: suitable

동형

IgG

NCBI 수납 번호

UniProt 수납 번호

배송 상태

wet ice

타겟 번역 후 변형

unmodified

유전자 정보

human ... MYH7B(57644)

특이성

Slow myosin heavy chain. Clearly identifies Type 1 fibers. Within skeletal muscle MAB1628 is specific for slow myosin heavy chain in a wide variety of species. It reacts strongly with rat and feline slow myosin heavy chain. MAB1628 also identifies beta (slow) myosin heavy chain in heart ventricles.

면역원

Epitope: slow muscle
Myosin purified from myofibrils isolated from histochemically mixed human skeletal muscle.

애플리케이션

Anti-Myosin Antibody, slow muscle, clone NOQ7.5.4D is an antibody against Myosin for use in RIA, WB, IH.
Immunohistochemistry: frozen and formalin fixed sections.

Immunoblotting

RIA

Optimal working dilutions must be determined by end user.

물리적 형태

Format: Purified

기타 정보

Concentration: Please refer to the Certificate of Analysis for the lot-specific concentration.

법적 정보

CHEMICON is a registered trademark of Merck KGaA, Darmstadt, Germany

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Storage Class Code

10 - Combustible liquids

WGK

WGK 2

Flash Point (°F)

Not applicable

Flash Point (°C)

Not applicable


시험 성적서(COA)

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문서 라이브러리 방문

Linda L Kusner et al.
Investigative ophthalmology & visual science, 51(1), 192-200 (2009-08-08)
Extraocular muscle (EOM) has a distinct skeletal muscle phenotype. The hypothesis for the study was that fibroblasts support the unique EOM phenotype and that perimysial fibroblasts derived from EOM have properties that distinguish them from fibroblasts derived from other skeletal
Lipid in skeletal muscle myotubes is associated to the donors' insulin sensitivity and physical activity phenotypes.
Bajpeyi, S; Myrland, CK; Covington, JD; Obanda, D; Cefalu, WT; Smith, SR; Rustan, AC; Ravussin, E
Obesity (Silver Spring, Md.) null
Jenny Lund et al.
Scientific reports, 8(1), 9814-9814 (2018-07-01)
Once assumed only to be a waste product of anaerobe glycolytic activity, lactate is now recognized as an energy source in skeletal muscles. While lactate metabolism has been extensively studied in vivo, underlying cellular processes are poorly described. This study
Camila Silva Foresto et al.
Journal of applied physiology (Bethesda, Md. : 1985), 121(3), 646-660 (2016-07-23)
Muscle loss occurs following injury and immobilization in adulthood and childhood, which impairs the rehabilitation process; however, far fewer studies have been conducted analyzing atrophic response in infants. This work investigated first the morphological and molecular mechanisms involved in immobilization-induced
Christian M Girgis et al.
Journal of cachexia, sarcopenia and muscle, 10(6), 1228-1240 (2019-06-22)
It has long been recognized that vitamin D deficiency is associated with muscle weakness and falls. Vitamin D receptor (VDR) is present at very low levels in normal muscle. Whether vitamin D plays a direct role in muscle function is

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