Actin 抗体 (Biotin)
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- 抗原 See all Actin (ACTA1) 抗体
- Actin (ACTA1) (Actin, alpha 1, Skeletal Muscle (ACTA1))
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适用
- 人, 小鼠, 大鼠
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宿主
- 小鼠
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克隆类型
- 单克隆
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标记
- This Actin antibody is conjugated to Biotin
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应用范围
- Western Blotting (WB), Immunohistochemistry (Paraffin-embedded Sections) (IHC (p))
- 交叉反应
- 人, 小鼠, 大鼠
- 纯化方法
- Purified by Protein A.
- 免疫原
- KLH conjugated synthetic peptide derived from human ACTA1
- 克隆位点
- 5F11
- 亚型
- IgG
- Top Product
- Discover our top product ACTA1 Primary Antibody
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anti-Actin, alpha 1, Skeletal Muscle (ACTA1) (AA 277-308), (C-Term) antibody
ACTA1 适用: 人, 小鼠, 大鼠 WB, IHC (p) 宿主: 兔 Polyclonal unconjugated
anti-Actin, alpha 1, Skeletal Muscle (ACTA1) antibodyACTA1 适用: 人, 大鼠, 兔, 斑马鱼, Pig, 小鸡, 猴 WB, ELISA, IHC, IHC (p), IHC (fro), IEM 宿主: 小鼠 Monoclonal HHF35 unconjugated
anti-Actin, alpha 1, Skeletal Muscle (ACTA1) (AA 346-375) antibodyACTA1 适用: 人 WB, ELISA, IHC, IF, FACS 宿主: 兔 Polyclonal unconjugated
anti-Actin, alpha 1, Skeletal Muscle (ACTA1) (AA 3-377) antibodyACTA1 适用: 人 WB, ELISA, IHC 宿主: 兔 Polyclonal unconjugated
anti-Actin, alpha 1, Skeletal Muscle (ACTA1) antibodyACTA1 适用: 人 WB, ELISA, IHC, IF, FACS 宿主: 兔 Monoclonal 25E3 unconjugated Recombinant Antibody
anti-Actin, alpha 1, Skeletal Muscle (ACTA1) (AA 1-129) antibodyACTA1 适用: 人, 斑马鱼, 鱼 WB, IHC, IHC (p) 宿主: 兔 Polyclonal unconjugated
anti-Actin, alpha 1, Skeletal Muscle (ACTA1) (AA 346-375), (C-Term) antibodyACTA1 适用: 人 WB, IHC (p), IF, FACS 宿主: 兔 Polyclonal RB35391 unconjugated
anti-Actin, alpha 1, Skeletal Muscle (ACTA1) antibodyACTA1 适用: 人 WB, IHC (p), FACS 宿主: 小鼠 Monoclonal 7C1 unconjugated
anti-Actin, alpha 1, Skeletal Muscle (ACTA1) (AA 7-377) antibodyACTA1 适用: 人 ELISA, IHC, IF 宿主: 兔 Polyclonal unconjugated
anti-Actin, alpha 1, Skeletal Muscle (ACTA1) antibodyACTA1 适用: 人, 小鼠, 大鼠 WB, ELISA, IHC 宿主: 兔 Polyclonal unconjugated
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- 应用备注
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WB 1:300-5000
IHC-P 1:200-400 - 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 for 12 months.
- 有效期
- 12 months
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- 抗原
- Actin (ACTA1) (Actin, alpha 1, Skeletal Muscle (ACTA1))
- 别名
- Actin, alpha skeletal muscle (ACTA1 产品)
- 别名
- ACTA antibody, ASMA antibody, CFTD antibody, CFTD1 antibody, CFTDM antibody, MPFD antibody, NEM1 antibody, NEM2 antibody, NEM3 antibody, acta antibody, asma antibody, cftd antibody, cftd1 antibody, cftdm antibody, mpfd antibody, nem1 antibody, AA959943 antibody, Acta-2 antibody, Acts antibody, Actsk-1 antibody, actc antibody, actc1 antibody, cfk antibody, hm:zeh0631 antibody, zeh0631 antibody, acta1 antibody, hm:zeh0293 antibody, zgc:112098 antibody, actin, alpha 1, skeletal muscle antibody, actin, alpha 1, skeletal muscle L homeolog antibody, actin, alpha 1b, skeletal muscle antibody, actin, muscle antibody, actin, alpha skeletal muscle antibody, actin, alpha 1a, skeletal muscle antibody, ACTA1 antibody, acta1.L antibody, acta1 antibody, Acta1 antibody, acta1b antibody, LOC100533357 antibody, LOC109479779 antibody, LOC109108280 antibody, acta1a antibody
- 背景
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Synonyms: ACTS_HUMAN, Actin, alpha skeletal muscle, Alpha-actin-1, ACTA1, ACTA, ASMA, CFTD, CFTD1, CFTDM, MPFD, NEM1, NEM2, NEM3, Actin alpha skeletal muscle, actin, alpha 1, skeletal muscle 1, actin, alpha 1, skeletal muscle, actina, actine, aktin, alpha Actin 1, alpha skeletal muscle Actin, alpha skeletal muscle, alpha-actin, Beta cytoskeletal actin, nemaline myopathy type 3.
Background: The product encoded by this gene belongs to the actin family of proteins, which are highly conserved proteins that play a role in cell motility, structure and integrity. Alpha, beta and gamma actin isoforms have been identified, with alpha actins being a major constituent of the contractile apparatus, while beta and gamma actins are involved in the regulation of cell motility. This actin is an alpha actin that is found in skeletal muscle. Mutations in this gene cause nemaline myopathy type 3, congenital myopathy with excess of thin myofilaments, congenital myopathy with cores, and congenital myopathy with fiber-type disproportion, diseases that lead to muscle fiber defects. [provided by RefSeq, Jul 2008]
- 基因ID
- 58
- UniProt
- P68133
- 途径
- Caspase Cascade in Apoptosis, Myometrial Relaxation and Contraction, Skeletal Muscle Fiber Development
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