TPM2 抗体 (AA 1-254)
Quick Overview for TPM2 抗体 (AA 1-254) (ABIN1885852)
抗原
See all TPM2 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 1-254
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纯化方法
- Purified by antigen-affinity chromatography.
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免疫原
- Recombinant protein fragment contain a sequence corresponding to a region within amino acids 1 and 254 of Tropomyosin 2
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anti-Tropomyosin-2 (TPM2) antibody
TPM2 适用: 人 WB, IHC, IP, IF 宿主: 兔 Polyclonal unconjugated
anti-Tropomyosin-2 (TPM2) antibodyTPM2 适用: 人, 小鼠, 大鼠 WB, ELISA, IHC 宿主: 兔 Polyclonal unconjugated
anti-Tropomyosin-2 (TPM2) (AA 1-284) antibodyTPM2 适用: 人 WB, ELISA, IHC (p) 宿主: 小鼠 Monoclonal 3C8 unconjugated
anti-Tropomyosin-2 (TPM2) (C-Term) antibodyTPM2 适用: 人, 小鼠, 大鼠, Cow, 犬, 兔, 斑马鱼, 豚鼠, 马, Pig, 绵羊 WB, IHC 宿主: 兔 Polyclonal unconjugated
anti-Tropomyosin-2 (TPM2) (C-Term) antibodyTPM2 适用: 人, 小鼠, 大鼠 WB, ELISA, IHC 宿主: 兔 Polyclonal unconjugated
anti-Tropomyosin-2 (TPM2) (C-Term) antibodyTPM2 适用: 人, 小鼠, 大鼠, 小鸡, Cow, 犬, 兔, 斑马鱼, 猴, 非洲爪蟾 WB, IHC, IHC (p) 宿主: 兔 Polyclonal unconjugated
anti-Tropomyosin-2 (TPM2) antibodyTPM2 适用: 人 WB, IHC (p) 宿主: 兔 Polyclonal unconjugated
anti-Tropomyosin-2 (TPM2) (AA 11-130) antibodyTPM2 适用: 人, 小鼠 WB, ELISA, IF (cc), IF (p), IHC (p), IHC (fro) 宿主: 兔 Polyclonal unconjugated
anti-Tropomyosin-2 (TPM2) (AA 1-284) antibodyTPM2 适用: 人 WB, IHC, IP, ICC 宿主: 兔 Polyclonal unconjugated
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应用备注
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Suggested dilutions:
Western blotting: 1.500-1.3000
Immunohistochemistry: 1.100-1.500 -
限制
- 仅限研究用
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状态
- Liquid
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缓冲液
- 0.1 M Tris-buffered saline with 10 % Glycerol (pH 7.0).0.01 % Thimerosal was added as a preservative.
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储存液
- Thimerosal (Merthiolate)
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注意事项
- Biohazard Informations: This product contains thimerosal which is hazardous.
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储存条件
- 4 °C/-20 °C
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储存方法
- Store at -20 °C for long term preservation (recommended). Store at 4 °C for short term use.
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- TPM2 (Tropomyosin-2 (TPM2))
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别名
- Tropomyosin 2
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背景
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This gene encodes beta-tropomyosin, a member of the actin filament binding protein family, and mainly expressed in slow, type 1 muscle fibers.Mutations in this gene can alter the expression of other sarcomeric tropomyosin proteins, and cause cap disease, nemaline myopathy and distal arthrogryposis syndromes.Alternatively spliced transcript variants encoding different isoforms have been found for this gene.
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分子量
- 33 kDa
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基因ID
- 7169
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NCBI登录号
- NM_213674, NP_998839
抗原
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