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MYH3 Polyclonal Antibody

说明书

BYab-05772

  • 20UL ¥460 50UL ¥945 100UL ¥1350
  • 货期: 3天左右

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宿主
反应性
应用
WB;ELISA
分子量(DA)
213kD
免疫原
Synthesized peptide derived from human protein . at AA range: 1770-1850
特异性
MYH3 Polyclonal Antibody detects endogenous levels of protein.
来源
Polyclonal, Rabbit,IgG
组成(Formulation)
Liquid in PBS containing 50% glycerol, and 0.02% sodium azide.
稀释比例
WB 1:500-2000 ELISA 1:5000-20000
纯化工艺(Immunogen)
The antibody was affinity-purified from rabbit antiserum by affinity-chromatography using epitope-specific immunogen.
浓度
1 mg/ml
背景(Background)
Myosin is a major contractile protein which converts chemical energy into mechanical energy through the hydrolysis of ATP. Myosin is a hexameric protein composed of a pair of myosin heavy chains (MYH) and two pairs of nonidentical light chains. This gene is a member of the MYH family and encodes a protein with an IQ domain and a myosin head-like domain. Mutations in this gene have been associated with two congenital contracture (arthrogryposis) syndromes, Freeman-Sheldon syndrome and Sheldon-Hall syndrome. [provided by RefSeq, Jul 2008],
功能
developmental stage:Abundantly present in fetal skeletal muscle and not present or barely detectable in heart and adult skeletal muscle.,disease:Defects in MYH3 are the cause of distal arthrogryposis type 2A (DA2A) [MIM:193700]; also known as Freeman-Sheldon syndrome (FSS). Distal arthrogryposis is a clinically and genetically heterogeneous group of disorders characterized by bone anomalies and joint contractures of the hands and feet, causing medially overlapping fingers, clenched fists, ulnar deviation of fingers, camptodactyly and positional foot deformities. It is a disorder of primary limb malformation without primary neurologic or muscle disease. DA2A is the most severe form of distal arthrogryposis. Affected individuals have contractures of the orofacial muscles, characterized by microstomia with pouting lips, H-shaped dimpling of the chin, deep nasolabial folds, and blepharophimo
基因名称(Gene Name)
MYH3
蛋白名称
Myosin-3 (Muscle embryonic myosin heavy chain) (Myosin heavy chain 3) (Myosin heavy chain, fast skeletal muscle, embryonic) (SMHCE)
简称
MYH3
其他名称
Fields
人基因ID
4621
人蛋白质序列数据库
P11055
小鼠基因ID
小鼠蛋白质序列数据库
P13541
大鼠基因ID
大鼠蛋白质序列数据库
P12847
细胞定位
Cytoplasm, myofibril. Thick filaments of the myofibrils.
组织表达
Expressed in fetal bone, thymus, placenta, heart, brain, and liver.
储存(Storage)
-20°C/1 year

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MYH3 Polyclonal Antibody

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