TPM2 抗体
Quick Overview for TPM2 抗体 (ABIN2856664)
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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交叉反应
- 人
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产品特性
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Rabbit polyclonal antibody to Tropomyosin 2 (tropomyosin 2 (beta))
Tropomyosin 2 antibody [N1C3] -
纯化方法
- Purified by antigen-affinity chromatography.
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免疫原
- Full length human Tropomyosin 2 Recombinant protein.
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亚型
- IgG
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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) (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
- WB: 1:500-1:3000. IHC-P: 1:100-1:1000. Optimal dilutions/concentrations should be determined by the researcher. Not tested in other applications.
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说明
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Positive Control: HeLa
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限制
- 仅限研究用
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状态
- Liquid
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浓度
- 0.66 mg/mL
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缓冲液
- 0.1M Tris-Glycine ( pH 7), 10 % Glycerol, 0.01 % Thimerosal
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储存液
- Thimerosal (Merthiolate)
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注意事项
- This product contains Thimerosal (Merthiolate): a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.
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储存条件
- 4 °C,-20 °C
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储存方法
- Store as concentrated solution. Centrifuge briefly prior to opening vial. For short-term storage (1-2 weeks), store at 4°C. For long-term storage, aliquot and store at -20°C or below. Avoid multiple freeze-thaw cycles.
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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.
Cellular Localization: Cytoplasm , cytoskeleton -
分子量
- 33 kDa
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基因ID
- 7169
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UniProt
- P07951
抗原
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