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GSC2 抗体 (AA 100-180)

This anti-GSC2 antibody is a 兔 多克隆 antibody detecting GSC2 in WB 和 ELISA. Suitable for 人 和 小鼠.
产品编号 ABIN7215174
发货至: 中国

Quick Overview for GSC2 抗体 (AA 100-180) (ABIN7215174)

抗原

See all GSC2 抗体
GSC2 (Goosecoid Homeobox 2 (GSC2))

适用

  • 9
  • 6
  • 2
  • 2
  • 1
  • 1
  • 1
  • 1
  • 1
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  • 1
人, 小鼠

宿主

  • 9

克隆类型

  • 9
多克隆

标记

  • 9
This GSC2 antibody is un-conjugated

应用范围

  • 8
  • 4
  • 2
  • 2
  • 1
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Western Blotting (WB), ELISA
  • 抗原表位

    • 6
    • 1
    • 1
    AA 100-180

    原理

    GSC2 Polyclonal Antibody

    特异性

    GSC2 Polyclonal Antibody detects endogenous levels of GSC2 protein.

    纯化方法

    The antibody was affinity-purified from rabbit antiserum by affinity-chromatography using epitope-specific immunogen

    免疫原

    Synthesized peptide derived from the C-terminal region of human GSC2 at AA range: 100-180

    亚型

    IgG
  • 应用备注

    Optimal working dilutions should be determined experimentally by the investigator. Suggested starting dilutions are as follows: WB (1:500-1:2000), ELISA (1:20000). Not yet tested in other applications.

    说明

    Primary Antibody

    限制

    仅限研究用
  • 状态

    Liquid

    浓度

    1 mg/mL

    缓冲液

    PBS containing 50 % Glycerol, 0.5 % BSA and 0.02 % Sodium Azide.

    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

    Stable for one year at -20°C from date of shipment. For maximum recovery of product, centrifuge the original vial after thawing and prior to removing the cap. Aliquot to avoid repeated freezing and thawing.
  • 抗原

    GSC2 (Goosecoid Homeobox 2 (GSC2))

    别名

    GSC2

    背景

    Rabbit Anti-GSC2 Polyclonal Antibody,GSC2, GSCL, Homeobox protein goosecoid-2, GSC-2, Homeobox protein goosecoid-like, GSC-L,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. GSC2 is expressed in a limited number of adult tissues, as well as in early human development.,Homeobox protein goosecoid-2

    分子量

    observerd band 25kDa

    基因ID

    2928

    UniProt

    O15499
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