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Myosin IIa (Phospho Ser1943) rabbit pAb
货 号:
YM-A16339
规 格:
50μL;100μL
种属反应:
Human,Rat,Mouse,
实验应用:
WB,IHC
产品详情
产品名称
Myosin IIa (Phospho Ser1943) rabbit pAb
产品货号
YM-A16339
规格
50μL;100μL
种属反应
Human,Rat,Mouse,
实验应用
WB,IHC
分子量
215kD
宿主
Rabbit
同种型
IgG
修饰
Phospho
推荐稀释比
WB 1:500-2000;IHC 1:50-300
组成
Liquid in PBS containing 50% glycerol, 0.5% BSA and 0.02% sodium azide.
纯化工艺
The antibody was affinity-purified from rabbit serum by affinity-chromatography using specific immunogen.
储存
-15°C to -25°C/1 year(Do not lower than -25°C)
浓度
1 mg/ml
克降性
Polyclonal
克隆号
免疫原
Synthesized phosho peptide around human Myosin IIa (Ser1943)
特异性
This antibody detects endogenous levels of Human Myosin IIa (phospho-Ser1943)
基因名称
MYH9
蛋白名称
Myosin IIa (Ser1943)
别名
Myosin-9;Cellular myosin heavy chain, type A;Myosin heavy chain 9;Myosin heavy chain, non-muscle IIa;Non-muscle myosin heavy chain A;NMMHC-A;Non-muscle myosin heavy chain IIa;NMMHC II-a;NMMHC-IIA;
基因ID-1
4627
SwissProt
P35579
背景
This gene encodes a conventional non-muscle myosin; this protein should not be confused with the unconventional myosin-9a or 9b (MYO9A or MYO9B). The encoded protein is a myosin IIA heavy chain that contains an IQ domain and a myosin head-like domain which is involved in several important functions, including cytokinesis, cell motility and maintenance of cell shape. Defects in this gene have been associated with non-syndromic sensorineural deafness autosomal dominant type 17, Epstein syndrome, Alport syndrome with macrothrombocytopenia, Sebastian syndrome, Fechtner syndrome and macrothrombocytopenia with progressive sensorineural deafness. [provided by RefSeq, Dec 2011],
细胞定位
Cytoplasm, cytoskeleton . Cytoplasm, cell cortex . Cytoplasmic vesicle, secretory vesicle, Cortical granule . Colocalizes with actin filaments at lamellipodia margins and at the leading edge of migrating cells (PubMed:20052411). In retinal pigment epithelial cells, predominantly localized to stress fiber-like structures with some localization to cytoplasmic puncta (PubMed:27331610). .
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