SHOX2 抗体 (AA 96-355)
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- 抗原 See all SHOX2 抗体
- SHOX2 (Short Stature Homeobox 2 (SHOX2))
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抗原表位
- AA 96-355
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适用
- 人
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宿主
- 兔
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克隆类型
- 多克隆
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标记
- This SHOX2 antibody is un-conjugated
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应用范围
- Western Blotting (WB)
- 序列
- ELDMGAAERS REPGSPRLTE GRRKPTKAEV QATLLLPGEA FRFLVSPELK DRKEDAKGME DEGQTKIKQR RSRTNFTLEQ LNELERLFDE THYPDAFMRE ELSQRLGLSE ARVQVWFQNR RAKCRKQENQ LHKGVLIGAA SQFEACRVAP YVNVGALRMP FQQDSHCNVT PLSFQVQAQL QLDSAVAHAH HHLHPHLAAH APYMMFPAPP FGLPLATLAA DSASAASVVA AAAAAKTTSK NSSIADLRLK AKKHAAALGL
- 交叉反应
- 人, 小鼠, 大鼠
- 产品特性
- Polyclonal Antibodies
- 免疫原
- Recombinant fusion protein containing a sequence corresponding to amino acids 96-355 of human SHOX2 (NP_003021.3).
- 亚型
- IgG
- Top Product
- Discover our top product SHOX2 Primary Antibody
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- 应用备注
- WB,1:500 - 1:2000
- 说明
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HIGH QUALITY
- 限制
- 仅限研究用
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- 状态
- Liquid
- 缓冲液
- PBS with 0.02 % sodium azide,50 % glycerol, pH 7.3.
- 储存液
- Sodium azide
- 注意事项
- This product contains Sodium azide: 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. Avoid freeze / thaw cycles.
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- 抗原
- SHOX2 (Short Stature Homeobox 2 (SHOX2))
- 别名
- SHOX2 (SHOX2 产品)
- 别名
- SHOX2 antibody, og12 antibody, shot antibody, og12x antibody, ogi2x antibody, OG12 antibody, OG12X antibody, SHOT antibody, 6330543G17Rik antibody, Og12x antibody, Prx3 antibody, zgc:65884 antibody, zgc:77344 antibody, short stature homeobox 2 antibody, SHOX2 antibody, shox2 antibody, Shox2 antibody
- 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.,SHOX2,OG12,OG12X,SHOT,Epigenetics & Nuclear Signaling,Transcription Factors,SHOX2
- 分子量
- 33 kDa/34 kDa/37 kDa
- 基因ID
- 6474
- UniProt
- O60902
- 途径
- Regulation of Muscle Cell Differentiation, Skeletal Muscle Fiber Development
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