SHOX2 Protein (Transcript Variant 3) (Myc-DYKDDDDK Tag)
SHOX2
宿主: 人
宿主: HEK-293 Cells
Recombinant
> 80 % as determined by SDS-PAGE and Coomassie blue staining
AbP, STD
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- 抗原 See all SHOX2 蛋白
- SHOX2 (Short Stature Homeobox 2 (SHOX2))
- 蛋白类型
- Recombinant
- 产品特性
- Transcript Variant 3
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宿主
- 人
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资源
- HEK-293 Cells
- 标记
- This SHOX2 protein is labelled with Myc-DYKDDDDK Tag.
- 应用范围
- Antibody Production (AbP), Standard (STD)
- 产品特性
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- Recombinant human SHOX2 / SHOT (transcript variant 3) protein expressed in HEK293 cells.
- Produced with end-sequenced ORF clone
- 纯度
- > 80 % as determined by SDS-PAGE and Coomassie blue staining
- Top Product
- Discover our top product SHOX2 蛋白
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Short Stature Homeobox 2 (SHOX2) (AA 117-204) protein (GST tag)
SHOX2 宿主: 人 宿主: 小麦胚 Recombinant ELISA, WB, AP, AA
Short Stature Homeobox 2 (SHOX2) (AA 1-355) protein (GST tag)SHOX2 宿主: 人 宿主: 小麦胚 Recombinant ELISA, WB, AP, AA
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- 应用备注
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Recombinant human proteins can be used for:
Native antigens for optimized antibody production
Positive controls in ELISA and other antibody assays - 说明
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The tag is located at the C-terminal.
- 限制
- 仅限研究用
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- 浓度
- 50 μg/mL
- 缓冲液
- 25 mM Tris.HCl, pH 7.3, 100 mM glycine, 10 % glycerol.
- 储存条件
- -80 °C
- 储存方法
- Store at -80°C. Thaw on ice, aliquot to individual single-use tubes, and then re-freeze immediately. Only 2-3 freeze thaw cycles are recommended.
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- 抗原
- SHOX2 (Short Stature Homeobox 2 (SHOX2))
- 别名
- Shox2,shot (SHOX2 产品)
- 别名
- SHOX2 Protein, og12 Protein, shot Protein, og12x Protein, ogi2x Protein, OG12 Protein, OG12X Protein, SHOT Protein, 6330543G17Rik Protein, Og12x Protein, Prx3 Protein, zgc:65884 Protein, zgc:77344 Protein, short stature homeobox 2 Protein, SHOX2 Protein, shox2 Protein, Shox2 Protein
- 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.
- 分子量
- 33.4 kDa
- NCBI登录号
- NP_001157150
- 途径
- Regulation of Muscle Cell Differentiation, Skeletal Muscle Fiber Development
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