SIX Homeobox 1 抗体
Quick Overview for SIX Homeobox 1 抗体 (ABIN2457949)
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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纯化方法
- Antibody is purified by peptide affinity chromatography method.
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免疫原
- Antibody produced in rabbits immunized with a synthetic peptide corresponding a region of human SIX1.
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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) (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) (Internal Region) antibodySIX1 适用: 人, 小鼠 WB, ELISA, IF, ICC 宿主: 兔 Polyclonal unconjugated
anti-SIX Homeobox 1 (SIX1) (AA 60-270) antibodySIX1 适用: 人 WB 宿主: 兔 Polyclonal unconjugated
anti-SIX Homeobox 1 (SIX1) (N-Term) antibodySIX1 适用: 人, 小鼠 WB 宿主: 兔 Polyclonal unconjugated
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应用备注
- SIX1 antibody can be used for detection of SIX1 by ELISA at 1:1562500. SIX1 antibody can be used for detection of SIX1 by western blot at 1 μg/mL, and HRP conjugated secondary antibody should be diluted 1:50,000 - 100,000.
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限制
- 仅限研究用
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状态
- Lyophilized
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溶解方式
- Add 50 ?L of distilled water. Final antibody concentration is 1 mg/mL.
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浓度
- 1 mg/mL
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缓冲液
- Antibody is lyophilized in PBS buffer with 2 % sucrose.
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注意事项
- As with any antibody avoid repeat freeze-thaw cycles.
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储存条件
- 4 °C/-20 °C
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储存方法
- For short periods of storage (days) store at 4 °C. For longer periods of storage, store SIX1 antibody at -20 °C.
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- SIX Homeobox 1 (SIX1)
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别名
- SIX1
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背景
- SIX1 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).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). Sequence Note: This RefSeq record was created from transcript and genomic sequence data because no single transcript was available for the full length of the gene. The extent of this transcript is supported by transcript alignments. Publication Note: This RefSeq record includes a subset of the publications that are available for this gene. Please see the Entrez Gene record to access additional publications.
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分子量
- 32 kDa
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基因ID
- 6495
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NCBI登录号
- NP_005973
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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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