产品货号:
Z27395
中文名称:
SPRYD2/CMYA5抗体
英文名称:
Anti-SPRYD2/CMYA5 Antibody
产品规格:
0.1mg
发货周期:
1~3天
产品价格:
询价
抗体名称 | Anti-SPRYD2/CMYA5 Antibody |
指标别名 | SPRYD2,TRIM76,C5orf10,DTNBP2,SPRYD2,Cardiomyopathy-associated protein 5,Dystrobrevin-binding protein 2 |
克隆性 | Polyclonal |
检验物种 | human,mouse,rat |
应用范围 | ELISA,WB,IHC,IF |
基因名称 | CMYA5 |
抗体来源 | Rabbit |
抗体类型 | IgG |
免疫原 | SPRYD2 antibody was raised against an 18 amino acid synthetic peptide near the carboxy terminus of human SPRYD2.The immunogen is located within amino acids 3810 - 3860 of SPRYD2. |
计算分子量 | 449kDa |
成分 | SPRYD2 Antibody is supplied in PBS containing 0.02% sodium azide. |
纯化方式 | SPRYD2 Antibody is affinity chromatography purified via peptide column. |
浓度 | 1mg/mL |
产品形态 | 溶液 |
保存条件 | 4℃可保存3个月,-20℃可保存1年。 |
背景资料 | SPRYD2,also known as Myospryn,was originally identified as the muscle-specific partner of dysbindin and as a Mef-2 target gene.It is a large scaffolding protein localized to the Z-disc/costamere region of striated muscle.SPRYD2 includes a noncanonical tripartite motif (TRIM-like) that lacks the RING domain but consists of a B-box coiled coil (BBC),fibronectin 3 (FN3) repeats,and SPRY domains.SPRYD2 interacts with desmin and calcineurin,and it has been suggested to play a role in the biogenesis of lysosome and negatively regulates slow-fiber-type transformation and skeletal muscle regeneration.SPRYD2 is dysregulated in Duchenne muscular dystrophy. |
Uniprot ID | Q8N3K9 |
基因名全称 | Cardiomyopathy associated 5 |
蛋白名全称 | Cardiomyopathy associated 5 |
推荐稀释比 | SPRYD2 antibody can be used for detection of SPRYD2 by Western blot at 1 ~ 2μg/mL.Antibody can also be used for immunohistochemistry starting at 2.5μg/mL.For immunofluorescence start at 20μg/mL.Antibody validated:Western Blot in mouse samples;Immunohistochemistry in mouse samples and Immunofluorescence in mouse samples.All other applications and species not yet tested. |
相关搜索:SPRYD2/CMYA5抗体,SPRYD2抗体,CMYA5多抗,Anti-SPRYD2/CMYA5 Antibody