SGCA 抗体 (AA 60-290)
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北京 101111
Quick Overview for SGCA 抗体 (AA 60-290) (ABIN1682687)
抗原
See all SGCA 抗体适用
宿主
克隆类型
标记
应用范围
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抗原表位
- AA 60-290
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序列
- ITYHAHLQGH PDLPRWLRYT QRSPHHPGFL YGSATPEDRG LQVIEVTAYN RDSFDTTRQR LVLEIGDPEG PLLPYQAEFL VRSHDAEEVL PSTPASRFLS ALGGLWEPGE LQLLNVTSAL DRGGRVPLPI EGRKEGVYIK VGSASPFSTC LKMVASPDSH ARCAQGQPPL LSCYDTLAPH FRVDWCNVTL VDKSVPEPAD EVPTPGDGIL EHDPFFCPPT EAPDRDFLVD A
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交叉反应
- 人, 小鼠, 大鼠
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产品特性
- Polyclonal Antibodies
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免疫原
- Recombinant fusion protein containing a sequence corresponding to amino acids 60-290 of human alpha Sarcoglycan (alpha Sarcoglycan (SGCA)) (NP_000014.1).
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亚型
- IgG
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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) (Internal Region) antibodySGCA 适用: 人, 小鼠, 大鼠 WB, ELISA, IHC, IF, ICC 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) antibodySGCA 适用: 人 WB, FACS 宿主: 兔 Monoclonal 24GB1460 unconjugated Recombinant Antibody
anti-Sarcoglycan, alpha (50kDa Dystrophin-Associated Glycoprotein) (SGCA) antibodySGCA 适用: 人, 小鼠, 大鼠 WB 宿主: 兔 Polyclonal unconjugated
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应用备注
- WB,1:500 - 1:2000,IF,1:50 - 1:200
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限制
- 仅限研究用
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缓冲液
- PBS with 0.02 % sodium azide,50 % glycerol, pH 7.3.
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储存液
- Sodium azide
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注意事项
- This product contains Sodium azide: a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.
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储存条件
- -20 °C
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储存方法
- Store at -20°C. Avoid freeze / thaw cycles.
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- SGCA (Sarcoglycan, alpha (50kDa Dystrophin-Associated Glycoprotein) (SGCA))
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别名
- SGCA
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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.,SGCA,50DAG,ADL,DAG2,DMDA2,LGMD2D,SCARMD1,adhalin,Signal Transduction,Cell Biology & Developmental Biology,Cytoskeleton,Extracellular Matrix,SGCA
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分子量
- 29 kDa/42 kDa
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基因ID
- 6442
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UniProt
- Q16586
抗原
-
