TPM3 抗体
Quick Overview for TPM3 抗体 (ABIN5698646)
抗原
See all TPM3 抗体适用
宿主
克隆类型
标记
应用范围
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免疫原
- tropomyosin 3
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亚型
- IgG
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anti-Tropomyosin 3 (TPM3) (AA 1-284) antibody
TPM3 适用: 人 WB, IF 宿主: 兔 Polyclonal unconjugated
anti-Tropomyosin 3 (TPM3) (AA 1-248) antibodyTPM3 适用: 人 WB, ELISA 宿主: 小鼠 Polyclonal unconjugated
anti-Tropomyosin 3 (TPM3) (AA 1-248) antibodyTPM3 适用: 人 WB, ELISA, IHC (p) 宿主: 小鼠 Monoclonal 2E4 unconjugated
anti-Tropomyosin 3 (TPM3) (AA 18-224) antibodyTPM3 适用: 人 IHC, ELISA, IF 宿主: 兔 Polyclonal unconjugated
anti-Tropomyosin 3 (TPM3) (AA 1-249) antibodyTPM3 适用: 人 WB, IHC, ELISA, IHC (p) 宿主: 小鼠 Monoclonal 2E4 unconjugated
anti-Tropomyosin 3 (TPM3) antibodyTPM3 适用: 人, 小鼠, 大鼠 WB, IF 宿主: 兔 Polyclonal unconjugated
anti-Tropomyosin 3 (TPM3) (N-Term) antibodyTPM3 适用: 人, 小鼠, 大鼠 WB, IHC, ELISA, IF, ICC 宿主: 兔 Polyclonal unconjugated
anti-Tropomyosin 3 (TPM3) (AA 6-248) antibodyTPM3 适用: 小鼠 WB, IHC, IP, ICC 宿主: 兔 Polyclonal unconjugated
anti-Tropomyosin 3 (TPM3) antibodyTPM3 适用: 人, 小鼠, 大鼠 WB, IHC, IF, IC 宿主: 兔 Polyclonal unconjugated
anti-Tropomyosin 3 (TPM3) antibodyTPM3 适用: 人, 小鼠 WB 宿主: 小鼠 Monoclonal 9C3 unconjugated
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应用备注
- Optimal working dilution should be determined by the investigator.
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说明
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mouse skeletal muscle tissue were subjected to SDS PAGE followed by western blot with FNab08890(TPM3 antibody) at dilution of 1:800
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限制
- 仅限研究用
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缓冲液
- PBS with 0.02 % sodium azide and 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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注意事项
- Avoid repeated freeze / thaw cycles.
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储存条件
- -20 °C
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有效期
- 12 months
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- TPM3 (Tropomyosin 3 (TPM3))
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别名
- TPM3
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背景
- Synonyms:CAPM1, CFTD, HEL-189, HEL-S-82p, hscp30,NEM1, OK/SW-cl.5, TM-5,TM3, TM30, TM30nm, TM5, TPMsk3, TRK Background:This gene encodes a member of the tropomyosin family of actin-binding proteins. Tropomyosins are dimers of coiled-coil proteins that provide stability to actin filaments and regulate access of other actin-binding proteins. Mutations in this gene result in autosomal dominant nemaline myopathy and other muscle disorders. This locus is involved in translocations with other loci, including anaplastic lymphoma receptor tyrosine kinase (ALK) and neurotrophic tyrosine kinase receptor type 1 (NTRK1), which result in the formation of fusion proteins that act as oncogenes. There are numerous pseudogenes for this gene on different chromosomes. Alternative splicing results in multiple transcript variants.
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基因ID
- 7169
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UniProt
- P06753
抗原
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