Abnova

SHOX2 Polyclonal Antibody, MaxPab™

Name: SHOX2 Polyclonal Antibody, MaxPab\u2122
Brand: Abnova
SKU: H00006474-B01P

查看其他6个SHOX2抗体

说明书

实验方案

问题与答案

技术支持

说明书

实验方案

问题与答案

技术支持

说明书

实验方案

问题与答案

技术支持

抗体检测数据 (1)

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SHOX2 Antibody (H00006474-B01P) in WB

Western Blot analysis of SHOX2 expression in transfected 293T cell line by SHOX2 MaxPab polyclonal antibody. Lane 1: SHOX2 transfected lysate(39.05 KDa). Lane 2: Non-transfected lysate. .

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产品信息

H00006474-B01P

应用

建议稀释比

已发表文章

免疫印迹 (WB)

1:500-1:1,000

产品规格

种属反应

Human

宿主/亚型

Mouse / IgG

分类

Polyclonal

类型

Antibody

抗原

SHOX2 (AAH08829.1, 1 a.a. approximately 355 a.a) full-length human protein.

偶联物

Unconjugated Unconjugated Unconjugated

形式

Liquid

浓度

0.5 mg/mL

纯化类型

Protein A

保存液

PBS, pH 7.4

内含物

no preservative

保存条件

-20°C, Avoid Freeze/Thaw Cycles

运输条件

Ambient (domestic); Wet ice (international)

产品详细信息

Product may be used with Western Blot (Transfected lysate).

The Isotype of this product is composed of an IgG Mixture.

Immunogen sequence: MEELTAFVSK SFDQKVKEKK EAITYREVLE SGPLRGAKEP TGCTEAGRDD RSSPAVRAAG GGGGGGGGGG GGGGGGGVGG GGAGGGAGGG RSPVRELDMG AAERSREPGS PRLTEGRRKP TKAEVQATLL LPGEAFRFLV SPELKDRKED AKGMEDEGQT KIKQRRSRTN FTLEQLNELE RLFDETHYPD AFMREELSQR LGLSEARVQV WFQNRRAKCR KQENQLHKGV LIGAASQFEA CRVAPYVNVG ALRMPFQQDS HCNVTPLSFQ VQAQLQLDSA VAHAHHHLHP HLAAHAPYMM FPAPPFGLPL ATLAADSASA ASVVAAAAAA KTTSKNSSIA DLRLKAKKHA AALGL

靶标信息

SHOX2 is a member of the homeo box family of genes that encode proteins containing a 60-amino acid residue motif that represents a DNA binding domain. Homeo box 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 homeo box genes. SHOX is a pseudoautosomal homeo box gene that is thought to be responsible for idiopathic short stature and implicated to play a role in the short stature phenotype of Turner syndrome patients. This gene is a member of the homeo box family of genes that encode proteins containing a 60-amino acid residue motif that represents a DNA binding domain. Homeo box 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 homeo box genes. SHOX is a pseudoautosomal homeo box gene that is thought to be responsible for idiopathic short stature and implicated to play a role 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 has been observed at this locus and two variants, each encoding a distinct isoform, have been identified.

仅用于科研。不用于诊断过程。未经明确授权不得转售。