SHOX2 抗体
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北京 101111
Quick Overview for SHOX2 抗体 (ABIN7264337)
抗原
See all SHOX2 抗体适用
宿主
克隆类型
标记
应用范围
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产品特性
- Polyclonal Antibody
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纯化方法
- Affinity purification
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免疫原
- Recombinant fusion protein of human SHOX2 (NP_003021.3).
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亚型
- IgG
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anti-Short Stature Homeobox 2 (SHOX2) (AA 117-204) antibody
SHOX2 适用: 人 WB, ELISA, RNAi 宿主: 小鼠 Monoclonal 1D1 unconjugated
anti-Short Stature Homeobox 2 (SHOX2) (AA 96-355) antibodySHOX2 适用: 人 WB 宿主: 兔 Polyclonal unconjugated
anti-Short Stature Homeobox 2 (SHOX2) (AA 72-331) antibodySHOX2 适用: 人 ELISA, IHC 宿主: 兔 Polyclonal unconjugated
anti-Short Stature Homeobox 2 (SHOX2) (AA 117-204) antibodySHOX2 适用: 人 WB, ELISA 宿主: 小鼠 Polyclonal unconjugated
anti-Short Stature Homeobox 2 (SHOX2) (AA 1-355) antibodySHOX2 适用: 人 IP 宿主: 兔 Polyclonal unconjugated
anti-Short Stature Homeobox 2 (SHOX2) (AA 1-355) antibodySHOX2 适用: 人 WB 宿主: 小鼠 Polyclonal unconjugated
anti-Short Stature Homeobox 2 (SHOX2) (AA 180-229) antibodySHOX2 适用: 人, 大鼠, 小鼠, Cow, 犬, 豚鼠, 斑马鱼, 马, 兔, 猴, Pig WB 宿主: 兔 Polyclonal unconjugated
anti-Short Stature Homeobox 2 (SHOX2) (AA 108-157) antibodySHOX2 适用: 人, 大鼠, Cow, 豚鼠, 猴, Pig WB 宿主: 兔 Polyclonal unconjugated
anti-Short Stature Homeobox 2 (SHOX2) (N-Term) antibodySHOX2 适用: 人, 大鼠, 小鼠, Cow, 犬, 豚鼠, 猴 WB 宿主: 兔 Polyclonal unconjugated
anti-Short Stature Homeobox 2 (SHOX2) (N-Term) antibodySHOX2 适用: 人, 大鼠, 小鼠, Cow, 犬, 豚鼠, 斑马鱼 WB 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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浓度
- 1 mg/mL
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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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- SHOX2 (Short Stature Homeobox 2 (SHOX2))
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别名
- SHOX2
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背景
- This gene is a member of the homeobox family of genes that encode proteins containing a 60-amino acid residue motif that represents a DNA binding domain. Homeobox genes have been characterized extensively as transcriptional regulators involved in pattern formation in both invertebrate and vertebrate species. Several human genetic disorders are caused by aberrations in human homeobox genes. This locus represents a pseudoautosomal homeobox gene that is thought to be responsible for idiopathic short stature, and it is implicated in the short stature phenotype of Turner syndrome patients. This gene is considered to be a candidate gene for Cornelia de Lange syndrome. Alternative splicing results in multiple transcript variants.
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分子量
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Observed_MW: 30 kDa
Calculated_MW: 33 kDa/34 kDa/37 kDa
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基因ID
- 6474
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UniProt
- O60902
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途径
- Regulation of Muscle Cell Differentiation, Skeletal Muscle Fiber Development
抗原
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