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GSC2 Protein (His tag)

GSC2 宿主: 人 宿主: 大肠杆菌(E. Coli) Recombinant > 80 % as determined by SDS-PAGE and Coomassie blue staining AbP, STD
产品编号 ABIN5505649
发货至: 中国
  • 抗原 See all GSC2 蛋白
    GSC2 (Goosecoid Homeobox 2 (GSC2))
    蛋白类型
    Recombinant
    宿主
    • 1
    • 1
    资源
    • 1
    • 1
    大肠杆菌(E. Coli)
    标记
    This GSC2 protein is labelled with His tag.
    应用范围
    Antibody Production (AbP), Standard (STD)
    产品特性
    • Recombinant human Purified recombinant protein of Human goosecoid homeobox 2 (GSC2), full length, with N-terminal HIS tag, expressed in E. coli, 50 μg (full length, N-term HIS tag) protein expressed in E.coli.
    • Produced with end-sequenced ORF clone
    纯化方法
    Purified
    纯度
    > 80 % as determined by SDS-PAGE and Coomassie blue staining
    Top Product
    Discover our top product GSC2 蛋白
  • 应用备注
    Recombinant human proteins can be used for:
    Native antigens for optimized antibody production
    Positive controls in ELISA and other antibody assays
    说明

    The tag is located at the N-terminal.

    限制
    仅限研究用
  • 浓度
    50 μg/mL
    缓冲液
    25 mM Tris, pH 8.0, 150 mM NaCl, 10 % glycerol, 1 % Sarkosyl.
    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.
  • 抗原
    GSC2 (Goosecoid Homeobox 2 (GSC2))
    别名
    goosecoid homeobox 2 (GSC2 产品)
    别名
    Gscl Protein, GSCL Protein, 4930568H22Rik Protein, GSC-2 Protein, goosecoid homeobox 2 Protein, goosecoid homebox 2 Protein, Gsc2 Protein, GSC2 Protein
    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.
    分子量
    21.4 kDa
    NCBI登录号
    NP_005306
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