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GSC2 Rabbit pAb

-YT2079

2 5
主要信息
Target

GSC2

Host Species

Rabbit

Reactivity

Human, Mouse

Applications

WB, ELISA

MW

25kD (Observed)

Conjugate/Modification

Unmodified

货号: YT2079
规格
价格
货期
数量
200μL
¥3,780.00
现货

0

100μL
¥2,300.00
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0

40μL
¥960.00
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详细信息
推荐稀释比
WB 1:500-1:2000; ELISA 1:20000; Not yet tested in other applications.
组成
Liquid in PBS containing 50% glycerol, 0.5% BSA and 0.02% sodium azide.
特异性
GSC2 Polyclonal Antibody detects endogenous levels of GSC2 protein.
纯化工艺
The antibody was affinity-purified from rabbit antiserum by affinity-chromatography using epitope-specific immunogen.
储存
-15°C to -25°C/1 year(Do not lower than -25°C)
浓度
1 mg/ml
实测条带
25kD
修饰
Unmodified
克隆性
Polyclonal
同种型
IgG
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抗原&靶点信息
免疫原:
The antiserum was produced against synthesized peptide derived from human GSC2. AA range:131-180
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特异性:
GSC2 Polyclonal Antibody detects endogenous levels of GSC2 protein.
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基因名称:
GSC2
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蛋白名称:
Homeobox protein goosecoid-2
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别名:
GSC2 ;
GSCL ;
Homeobox protein goosecoid-2 ;
GSC-2 ;
Homeobox protein goosecoid-like ;
GSC-L
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数据库链接:
Organism 基因 ID SwissProt
Human 2928; O15499;
Mouse P56916;
背景:
Goosecoidlike (GSCL), a homeodomain-containing gene, resides in the critical region for VCFS/DGS on 22q11. Velocardiofacial syndrome (VCFS) is a developmental disorder characterized by conotruncal heart defects, craniofacial anomalies, and learning disabilities. VCFS is phenotypically related to DiGeorge syndrome (DGS) and both syndromes are associated with hemizygous 22q11 deletions. Because many of the tissues and structures affected in VCFS/DGS derive from the pharyngeal arches of the developing embryo, it is believed that haploinsufficiency of a gene involved in embryonic development may be responsible for its etiology. The gene is expressed in a limited number of adult tissues, as well as in early human development. [provided by RefSeq, Jul 2008],
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功能:
developmental stage:Expressed in early human development as well as in a limited number of adult tissues.,Disease:May play a part in the etiology of the velocardiofacial/DiGeorge syndrome (VCFS/DGS), a developmental disorder characterized by structural and functional palate anomalies, conotruncal cardiac malformations, immunodeficiency, hypocalcemia, and typical facial anomalies. Most cases result from a deletion of chromosome 22q11.2 (the DiGeorge syndrome chromosome region, or DGCR).,Function:May have a role in development. May regulate its own transcription. May bind the bicoid consensus sequence TAATCC.,similarity:Belongs to the paired homeobox family. Bicoid subfamily.,similarity:Contains 1 homeobox DNA-binding domain.,tissue specificity:Detected in adult testis and pituitary, and in 9-10 week fetal tissue (thorax). Probably expressed in other tissues at low levels.,
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细胞定位:
Nucleus .
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组织表达:
Detected in adult testis and pituitary, and in 9-10 week fetal tissue (thorax). Probably expressed in other tissues at low levels.
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货号: YT2079
规格
价格
货期
数量
200μL
¥3,780.00
现货

0

100μL
¥2,300.00
现货

0

40μL
¥960.00
现货

0

加入购物车

已收藏

收藏

定制服务咨询

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