SIX Homeobox 1 抗体 (AA 60-270)
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Quick Overview for SIX Homeobox 1 抗体 (AA 60-270) (ABIN6147805)
抗原
See all SIX Homeobox 1 (SIX1) 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 60-270
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序列
- RGNFRELYKI LESHQFSPHN HPKLQQLWLK AHYVEAEKLR GRPLGAVGKY RVRRKFPLPR TIWDGEETSY CFKEKSRGVL REWYAHNPYP SPREKRELAE ATGLTTTQVS NWFKNRRQRD RAAEAKEREN TENNNSSSNK QNQLSPLEGG KPLMSSSEEE FSPPQSPDQN SVLLLQGNMG HARSSNYSLP GLTASQPSHG LQTHQHQLQD S
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交叉反应
- 人, 大鼠
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产品特性
- Polyclonal Antibodies
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免疫原
- Recombinant fusion protein containing a sequence corresponding to amino acids 60-270 of human SIX1 (NP_005973.1).
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亚型
- IgG
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anti-SIX Homeobox 1 (SIX1) antibody
SIX1 适用: 人, 小鼠, 大鼠 WB, IHC, IF 宿主: 兔 Polyclonal unconjugated
anti-SIX Homeobox 1 (SIX1) (Middle Region) antibodySIX1 适用: 人, 小鼠, 大鼠, 犬, 豚鼠, 马, 兔, Cow, 绵羊 WB, IHC 宿主: 兔 Polyclonal unconjugated
anti-SIX Homeobox 1 (SIX1) (AA 144-262) antibodySIX1 适用: 人 WB, ELISA, IHC 宿主: 兔 Polyclonal unconjugated
anti-SIX Homeobox 1 (SIX1) (AA 69-102) antibodySIX1 适用: 人, 小鼠 WB 宿主: 兔 Polyclonal RB53311 unconjugated
anti-SIX Homeobox 1 (SIX1) (Internal Region) antibodySIX1 适用: 人, 小鼠 WB, ELISA, IF, ICC 宿主: 兔 Polyclonal unconjugated
anti-SIX Homeobox 1 (SIX1) (C-Term) antibodySIX1 适用: 人, 小鼠, 大鼠, 犬, 豚鼠, 马, Cow, 绵羊, Pig, Bat, Hamster, 猴 WB 宿主: 兔 Polyclonal unconjugated
anti-SIX Homeobox 1 (SIX1) (AA 1-284) antibodySIX1 适用: 人 ELISA 宿主: 小鼠 Monoclonal 3C7 unconjugated
anti-SIX Homeobox 1 (SIX1) (N-Term) antibodySIX1 适用: 人, 小鼠 WB 宿主: 兔 Polyclonal unconjugated
anti-SIX Homeobox 1 (SIX1) (N-Term) antibodySIX1 适用: 人, 小鼠, 大鼠, 犬, 豚鼠, 马, 兔, Cow, 绵羊, 斑马鱼 WB, IHC 宿主: 兔 Polyclonal unconjugated
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应用备注
- WB,1:500 - 1:2000
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限制
- 仅限研究用
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状态
- Liquid
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缓冲液
- PBS with 0.02 % sodium azide,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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储存条件
- -20 °C
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储存方法
- Store at -20°C. Avoid freeze / thaw cycles.
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- SIX Homeobox 1 (SIX1)
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别名
- SIX1
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背景
- The protein encoded by this gene is a homeobox protein that is similar to the Drosophila 'sine oculis' gene product. This gene is found in a cluster of related genes on chromosome 14 and is thought to be involved in limb development. Defects in this gene are a cause of autosomal dominant deafness type 23 (DFNA23) and branchiootic syndrome type 3 (BOS3).,SIX1,BOS3,DFNA23,TIP39,SIX1
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分子量
- 32 kDa
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基因ID
- 6495
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UniProt
- Q15475
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途径
- Sensory Perception of Sound, Regulation of Muscle Cell Differentiation, Tube Formation, Skeletal Muscle Fiber Development
抗原
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