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MuSK (phospho Tyr755) Rabbit Polyclonal Antibody

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产品基本信息

产品货号
BD-PP0510
产品名称
MuSK (phospho Tyr755) Rabbit Polyclonal Antibody
别名
MUSK; Muscle; skeletal receptor tyrosine-protein kinase; Muscle-specific tyrosine-protein kinase receptor; MuSK; Muscle-specific kinase receptor
类别
常规抗体
基因名称
MUSK
蛋白名称
Muscle, skeletal receptor tyrosine-protein kinase
推荐应用
WB
反应种属
Human,Mouse,Rat
浓度
1 mg/ml
存储缓冲液
Liquid in PBS containing 50% glycerol, 0.5% BSA and 0.02% New type preservative N.
Human Gene ID
4593
Human Gene Link
http://www.ncbi.nlm.nih.gov/sites/entrez?db=gene&term=4593
Human Swissprot No.
O15146
Human Swissprot Link
http://www.uniprot.org/uniprotkb/O15146/entry
Mouse Gene ID
18198
Mouse Gene Link
http://www.ncbi.nlm.nih.gov/sites/entrez?db=gene&term=18198
Mouse Swissprot No.
Q61006
Mouse Swissprot Link
http://www.uniprot.org/uniprot/Q61006
Rat Gene ID
81725
Rat Gene Link
http://www.ncbi.nlm.nih.gov/sites/entrez?db=gene&term=81725
Rat Swissprot No.
Q62838
Rat Swissprot Link
http://www.uniprot.org/uniprot/Q62838
免疫原
Synthesized phospho-peptide around the phosphorylation site of human MuSK (phospho Tyr755)
特异性
Phospho-MuSK (Y755) Polyclonal Antibody detects endogenous levels of MuSK protein only when phosphorylated at Y755.
稀释度
WB 1:500-2000;IHC-p 1:50-300; ELISA 2000-20000
预测分子量
97kD
运输及保存条件
-20°C/1 year
宿主
Polyclonal, Rabbit,IgG
背景介绍
This gene encodes a muscle-specific tyrosine kinase receptor. The encoded protein may play a role in clustering of the acetylcholine receptor in the postsynaptic neuromuscular junction. Mutations in this gene have been associated with congenital myasthenic syndrome. Alternatively spliced transcript variants have been described.[provided by RefSeq, Oct 2009],
细胞定位
Cell junction, synapse, postsynaptic cell membrane ; Single-pass type I membrane protein . Colocalizes with acetylcholine receptors (AChR) to the postsynaptic cell membrane of the neuromuscular junction. .
功能
catalytic activity:ATP + a [protein]-L-tyrosine = ADP + a [protein]-L-tyrosine phosphate.,disease:Defects in MUSK is a cause of autosomal recessive congenital myasthenic syndrome (CMS) [MIM:608931]. Congenital myasthenic syndromes are inherited disorders of neuromuscular transmission that stem from mutations in presynaptic, synaptic, or postsynaptic proteins. MUSK mutations lead to decreased agrin-dependent AChR aggregation, a critical step in the formation of the neuromuscular junction.,function:Receptor tyrosine kinase that is a key mediator of agrin's action and is involved in neuromuscular junction (NMJ) organization.,online information:MuSK entry,similarity:Belongs to the protein kinase superfamily. Tyr protein kinase family.,similarity:Contains 1 FZ (frizzled) domain.,similarity:Contains 1 protein kinase domain.,similarity:Contains 3 Ig-like C2-type (immunoglobulin-like) domains.,subunit:Interacts with DOK7, which probably regulates its activity.,
期货
现货
纯化
The antibody was affinity-purified from rabbit antiserum by affinity-chromatography using epitope-specific immunogen.

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