-
- 抗原 See all SGCA 抗体
- SGCA (Sarcoglycan, alpha (50kDa Dystrophin-Associated Glycoprotein) (SGCA))
-
适用
- 人, 小鼠, 大鼠
-
宿主
- 兔
-
克隆类型
- 多克隆
-
标记
- This SGCA antibody is un-conjugated
-
应用范围
- Western Blotting (WB)
- 产品特性
- Polyclonal Antibody
- 纯化方法
- Affinity purification
- 免疫原
- Recombinant fusion protein of human SGCA (NP_000014.1).
- 亚型
- IgG
- Top Product
- Discover our top product SGCA Primary Antibody
-
anti-Sarcoglycan, alpha (50kDa Dystrophin-Associated Glycoprotein) (SGCA) (AA 24-290) antibody
SGCA 适用: 人 WB, ELISA, IHC, IF 宿主: 兔 Polyclonal unconjugated
anti-Sarcoglycan, alpha (50kDa Dystrophin-Associated Glycoprotein) (SGCA) (AA 60-290) antibodySGCA 适用: 人 WB, IF 宿主: 兔 Polyclonal unconjugated
anti-Sarcoglycan, alpha (50kDa Dystrophin-Associated Glycoprotein) (SGCA) (AA 26-133) antibodySGCA 适用: 人 WB, ELISA 宿主: 小鼠 Monoclonal 3C4 unconjugated
anti-Sarcoglycan, alpha (50kDa Dystrophin-Associated Glycoprotein) (SGCA) (Internal Region) antibodySGCA 适用: 人, 小鼠, 大鼠 WB, ELISA, IHC, IF, ICC 宿主: 兔 Polyclonal unconjugated
-
- 应用备注
- WB 1:500-1:2000
- 限制
- 仅限研究用
-
- 状态
- Liquid
- 浓度
- 1 mg/mL
- 缓冲液
- PBS with 0.02 % sodium azide, 50 % glycerol, pH 7.3
- 储存液
- Sodium azide
- 注意事项
- This product contains Sodium azide: a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.
- 储存条件
- -20 °C
- 储存方法
- Store at -20°C. Avoid freeze / thaw cycles.
-
- 抗原
- SGCA (Sarcoglycan, alpha (50kDa Dystrophin-Associated Glycoprotein) (SGCA))
- 别名
- SGCA (SGCA 产品)
- 别名
- Sgca antibody, 50-DAG antibody, A2 antibody, ADL antibody, DAG2 antibody, DMDA2 antibody, LGMD2D antibody, SCARMD1 antibody, adhalin antibody, 50DAG antibody, Asg antibody, sarcoglycan alpha antibody, sarcoglycan, alpha (dystrophin-associated glycoprotein) antibody, sarcoglycan, alpha antibody, SGCA antibody, Sgca antibody
- 背景
- This gene encodes a component of the dystrophin-glycoprotein complex (DGC), which is critical to the stability of muscle fiber membranes and to the linking of the actin cytoskeleton to the extracellular matrix. Its expression is thought to be restricted to striated muscle. Mutations in this gene result in type 2D autosomal recessive limb-girdle muscular dystrophy. Multiple transcript variants encoding different isoforms have been found for this gene.
- 分子量
-
Observed_MW: 43 kDa
Calculated_MW: 29 kDa/42 kDa
- 基因ID
- 6442
- UniProt
- Q16586
-
You are here:
