Anti-Myosin heavy chain Antibody (CAB4963)

(No reviews yet) Write a Review
SKU:
CAB4963
Product type:
Antibody
Antibody Type:
Monoclonal Antibody
Reactivity:
Mouse
Reactivity:
Rat
Host Species:
Rabbit
Isotype:
IgG
Synonyms:
CMD1S
Synonyms:
CMH1
Synonyms:
MPD1
Synonyms:
MYHCB
Synonyms:
SPMD
Synonyms:
SPMM
€0.00
Frequently bought together:

Description

I抗体名:Myosin heavy chain Rabbit mAb
抗体コード:CAB4963
サイズ:20uL, 50uL, 100uL
同義語:CMD1S, CMH1, MPD1, MYHCB, SPMD, SPMM
申し込み:WB, IHC, IF
反応性:Mouse, Rat
宿主種:Rabbit
免疫原:A synthesized peptide derived from human Myosin heavy chain
申し込み:WB, IHC, IF
推奨される希釈:WB 1:500 - 1:2000 IHC 1:50 - 1:200 IF 1:50 - 1:200
反応性:Mouse, Rat
ポジティブサンプル:Mouse lung, Mouse skeletal muscle, Rat heart
免疫原:A synthesized peptide derived from human Myosin heavy chain
精製方法:Affinity purification
保管所:Store at -20°C. Avoid freeze / thaw cycles. Buffer: PBS with 0.02% sodium azide, 0.05% BSA, 50% glycerol, pH7.3.
アイソタイプ:IgG
順序:Email for sequence
遺伝子ID:4625/4624
Uniprot:P12883/P13533
セルラーロケーション:Cytoplasm, myofibril
計算された分子量:224kDa
観察された分子量:250KDa
UniProt Protein Function:MYH7: Muscle contraction. Defects in MYH7 are the cause of familial hypertrophic cardiomyopathy type 1 (CMH1). Familial hypertrophic cardiomyopathy is a hereditary heart disorder characterized by ventricular hypertrophy, which is usually asymmetric and often involves the interventricular septum. The symptoms include dyspnea, syncope, collapse, palpitations, and chest pain. They can be readily provoked by exercise. The disorder has inter- and intrafamilial variability ranging from benign to malignant forms with high risk of cardiac failure and sudden cardiac death. Defects in MYH7 are the cause of myopathy myosin storage (MYOMS). In this disorder, muscle biopsy shows type 1 fiber predominance and increased interstitial fat and connective tissue. Inclusion bodies consisting of the beta cardiac myosin heavy chain are present in the majority of type 1 fibers, but not in type 2 fibers. Defects in MYH7 are the cause of scapuloperoneal myopathy MYH7-related (SPMM); also known as scapuloperoneal syndrome myopathic type. SPMM is a progressive muscular atrophia beginning in the lower legs and affecting the shoulder region earlier and more severely than distal arm. Defects in MYH7 are a cause of cardiomyopathy dilated type 1S (CMD1S). Dilated cardiomyopathy is a disorder characterized by ventricular dilation and impaired systolic function, resulting in congestive heart failure and arrhythmia. Patients are at risk of premature death. Defects in MYH7 are the cause of myopathy distal type 1 (MPD1). MPD1 is a muscular disorder characterized by early-onset selective weakness of the great toe and ankle dorsiflexors, followed by weakness of the finger extensors. Mild proximal weakness occasionally develops years later after the onset of the disease.
UniProt Protein Details:

Protein type:Motility/polarity/chemotaxis; Motor

Chromosomal Location of Human Ortholog: 14q12

Cellular Component: nucleoplasm; sarcomere; focal adhesion; cytoplasm; stress fiber; muscle myosin complex; myosin complex; Z disc

Molecular Function:microfilament motor activity; calmodulin binding; protein binding; ATPase activity; actin-dependent ATPase activity; actin binding; ATP binding

Biological Process: adult heart development; striated muscle contraction; muscle contraction; regulation of heart rate; metabolic process; ventricular cardiac muscle morphogenesis; regulation of the force of heart contraction; muscle filament sliding

Disease: Myopathy, Distal, 1; Scapuloperoneal Myopathy, Myh7-related; Myopathy, Myosin Storage; Cardiomyopathy, Dilated, 1s; Cardiomyopathy, Familial Hypertrophic, 1; Myopathy, Myosin Storage, Autosomal Recessive; Myopathy, Congenital, With Fiber-type Disproportion

NCBI Summary:Muscle myosin is a hexameric protein containing 2 heavy chain subunits, 2 alkali light chain subunits, and 2 regulatory light chain subunits. This gene encodes the beta (or slow) heavy chain subunit of cardiac myosin. It is expressed predominantly in normal human ventricle. It is also expressed in skeletal muscle tissues rich in slow-twitch type I muscle fibers. Changes in the relative abundance of this protein and the alpha (or fast) heavy subunit of cardiac myosin correlate with the contractile velocity of cardiac muscle. Its expression is also altered during thyroid hormone depletion and hemodynamic overloading. Mutations in this gene are associated with familial hypertrophic cardiomyopathy, myosin storage myopathy, dilated cardiomyopathy, and Laing early-onset distal myopathy. [provided by RefSeq, Jul 2008]
UniProt Code:P12883
NCBI GenInfo Identifier:83304912
NCBI Gene ID:4625
NCBI Accession:P12883.5
UniProt Secondary Accession:P12883,Q14836, Q14837, Q14904, Q16579, Q2M1Y6, Q92679 Q9H1D5, Q9UDA2, Q9UMM8, A2TDB6, B6D424,
UniProt Related Accession:P12883
Molecular Weight:223,097 Da
NCBI Full Name:Myosin-7
NCBI Synonym Full Names:myosin, heavy chain 7, cardiac muscle, beta
NCBI Official Symbol:MYH7  
NCBI Official Synonym Symbols:CMH1; MPD1; SPMD; SPMM; CMD1S; MYHCB  
NCBI Protein Information:myosin-7
UniProt Protein Name:Myosin-7
UniProt Synonym Protein Names:Myosin heavy chain 7; Myosin heavy chain slow isoform; MyHC-slow; Myosin heavy chain, cardiac muscle beta isoform; MyHC-beta
Protein Family:Myosin
UniProt Gene Name:MYH7  
UniProt Entry Name:MYH7_HUMAN
View AllClose

View AllClose

Related Products