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- 抗原 See all TNNT1 抗体
- TNNT1 (Slow Skeletal Troponin T (TNNT1))
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适用
- 人, 小鼠
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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 TNNT1 antibody is un-conjugated
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应用范围
- Western Blotting (WB), ELISA
- 纯化方法
- Antibody is purified by peptide affinity chromatography method.
- 免疫原
- Antibody produced in rabbits immunized with a synthetic peptide corresponding a region of human TNNT1.
- Top Product
- Discover our top product TNNT1 Primary Antibody
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anti-Slow Skeletal Troponin T (TNNT1) (AA 1-261) antibody
TNNT1 适用: 小鼠 WB, IHC, IP, ICC 宿主: 兔 Polyclonal unconjugated
anti-Slow Skeletal Troponin T (TNNT1) (AA 1-259) antibodyTNNT1 适用: 人 WB, IHC, IP, ICC 宿主: 兔 Polyclonal unconjugated
anti-Slow Skeletal Troponin T (TNNT1) antibodyTNNT1 适用: 人, 小鼠 WB, IHC, ELISA 宿主: 兔 Polyclonal unconjugated
anti-Slow Skeletal Troponin T (TNNT1) (AA 1-251) antibodyTNNT1 适用: 人 WB 宿主: 小鼠 Polyclonal unconjugated
anti-Slow Skeletal Troponin T (TNNT1) (AA 1-228) antibodyTNNT1 适用: 大鼠 WB, IHC, ICC 宿主: 兔 Polyclonal unconjugated
anti-Slow Skeletal Troponin T (TNNT1) antibodyTNNT1 适用: 兔 WB, IHC (p), IHC (fro) 宿主: 小鼠 Monoclonal JLT-12 unconjugated
anti-Slow Skeletal Troponin T (TNNT1) (AA 1-251) antibodyTNNT1 适用: 人 WB 宿主: 兔 Polyclonal unconjugated
anti-Slow Skeletal Troponin T (TNNT1) (N-Term) antibodyTNNT1 适用: 人, 小鼠, 大鼠 WB, ELISA, ICC, IF 宿主: 兔 Polyclonal unconjugated
anti-Slow Skeletal Troponin T (TNNT1) (Internal Region) antibodyVerified TNNT1 适用: 人 WB, IHC, ELISA 宿主: 山羊 Polyclonal unconjugated
anti-Slow Skeletal Troponin T (TNNT1) (C-Term) antibodyTNNT1 适用: 人, 小鼠, 大鼠, Cow, 犬, 豚鼠, 马, Pig, 猴 WB 宿主: 兔 Polyclonal unconjugated
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- 应用备注
- TNNT1 antibody can be used for detection of TNNT1 by ELISA at 1:312500. TNNT1 antibody can be used for detection of TNNT1 by western blot at 1 μg/mL, and HRP conjugated secondary antibody should be diluted 1:50,000 - 100,000.
- 限制
- 仅限研究用
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- 状态
- Lyophilized
- 溶解方式
- Add 50 ?L of distilled water. Final antibody concentration is 1 mg/mL.
- 浓度
- 1 mg/mL
- 缓冲液
- Antibody is lyophilized in PBS buffer with 2 % sucrose.
- 注意事项
- As with any antibody avoid repeat freeze-thaw cycles.
- 储存条件
- 4 °C/-20 °C
- 储存方法
- For short periods of storage (days) store at 4 °C. For longer periods of storage, store TNNT1 antibody at -20 °C.
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- 抗原
- TNNT1 (Slow Skeletal Troponin T (TNNT1))
- 别名
- TNNT1 (TNNT1 产品)
- 别名
- ANM antibody, NEM5 antibody, STNT antibody, TNT antibody, TNTS antibody, TNNI1 antibody, AW146156 antibody, Tnt antibody, sTnT antibody, ssTnT antibody, Fang2 antibody, tnTs antibody, Tnnt antibody, zgc:193831 antibody, zgc:193865 antibody, troponin T1, slow skeletal type antibody, troponin I1, slow skeletal type antibody, troponin T1, skeletal, slow antibody, troponin T1, slow skeletal type S homeolog antibody, troponin T type 1 (skeletal, slow) antibody, TNNT1 antibody, TNNI1 antibody, Tnnt1 antibody, tnnt1.S antibody, tnnt1 antibody
- 背景
- TNNT1 is a protein that is a subunit of troponin, which is a regulatory complex located on the thin filament of the sarcomere. This complex regulates striated muscle contraction in response to fluctuations in intracellular calcium concentration. This complex is composed of three subunits: troponin C, which binds calcium, troponin T, which binds tropomyosin, and troponin I, which is an inhibitory subunit. This protein is the slow skeletal troponin T subunit. Mutations in this gene cause nemaline myopathy type 5, also known as Amish nemaline myopathy, a neuromuscular disorder characterized by muscle weakness and rod-shaped, or nemaline, inclusions in skeletal muscle fibers which affects infants, resulting in death due to respiratory insufficiency, usually in the second year.This gene encodes a protein that is a subunit of troponin, which is a regulatory complex located on the thin filament of the sarcomere. This complex regulates striated muscle contraction in response to fluctuations in intracellular calcium concentration. This complex is composed of three subunits: troponin C, which binds calcium, troponin T, which binds tropomyosin, and troponin I, which is an inhibitory subunit. This protein is the slow skeletal troponin T subunit. Mutations in this gene cause nemaline myopathy type 5, also known as Amish nemaline myopathy, a neuromuscular disorder characterized by muscle weakness and rod-shaped, or nemaline, inclusions in skeletal muscle fibers which affects infants, resulting in death due to respiratory insufficiency, usually in the second year. Multiple transcript variants encoding different isoforms have been found for this gene.
- 分子量
- 33 kDa
- 基因ID
- 7138
- NCBI登录号
- NP_003274
- UniProt
- P13805
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