SNTG2 抗体 (AA 181-280) (Cy5)
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- 抗原 See all SNTG2 抗体
- SNTG2 (Syntrophin, gamma 2 (SNTG2))
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抗原表位
- AA 181-280
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适用
- 人
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宿主
- 兔
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克隆类型
- 多克隆
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标记
- This SNTG2 antibody is conjugated to Cy5
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应用范围
- Western Blotting (WB), Immunofluorescence (Paraffin-embedded Sections) (IF (p)), Immunofluorescence (Cultured Cells) (IF (cc))
- 预测反应
- Human,Mouse,Rat
- 纯化方法
- Purified by Protein A.
- 免疫原
- KLH conjugated synthetic peptide derived from human SNTG2
- 亚型
- IgG
- Top Product
- Discover our top product SNTG2 Primary Antibody
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anti-Syntrophin, gamma 2 (SNTG2) (C-Term) antibody
Verified SNTG2 适用: 人 WB, ELISA 宿主: 山羊 Polyclonal unconjugated
anti-Syntrophin, gamma 2 (SNTG2) (AA 143-324) antibodySNTG2 适用: 人 WB, ELISA, IHC 宿主: 兔 Polyclonal unconjugated
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- 应用备注
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IF(IHC-P) 1:50-200
IF(IHC-F) 1:50-200
IF(ICC) 1:50-200 - 限制
- 仅限研究用
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- 状态
- Liquid
- 浓度
- 1 μg/μL
- 缓冲液
- Aqueous buffered solution containing 0.01M TBS ( pH 7.4) with 1 % BSA, 0.03 % Proclin300 and 50 % Glycerol.
- 储存液
- ProClin
- 注意事项
- This product contains ProClin: 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. Aliquot into multiple vials to avoid repeated freeze-thaw cycles.
- 有效期
- 12 months
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- 抗原
- SNTG2 (Syntrophin, gamma 2 (SNTG2))
- 别名
- SNTG2/Syntrophin 5 (SNTG2 产品)
- 别名
- MGC84699 antibody, SNTG2 antibody, G2SYN antibody, SYN5 antibody, 2210008K22Rik antibody, 9530013L23 antibody, BB121248 antibody, syntrophin, gamma 2 L homeolog antibody, syntrophin gamma 2 antibody, syntrophin, gamma 2 antibody, sntg2.L antibody, SNTG2 antibody, Sntg2 antibody
- 背景
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Synonyms: G2SYN, Gamma2-syntrophin, SNTG2, SYN5, Syntrophin-5, Syntrophin5, Syntrophin 5, Syntrophin gamma 2, SNTG2_HUMAN.
Background: Syntrophins are cytoplasmic peripheral membrane proteins that bind to components of mechanosenstive sodium channels and the extreme carboxy-terminal domain of dystrophin and dystrophin-related proteins. The PDZ domain of this protein product interacts with a protein component of a mechanosensitive sodium channel that affects channel gating. Absence or reduction of this protein product has been associated with Duchenne muscular dystrophy.
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