电话:
400-7060-959
传真:
+86 10 56315212-8813
电子邮件:
orders@antibodies-online.cn

TACSTD2 Protein (His tag)

TACSTD2 宿主: 大鼠 宿主: HEK-293 Cells Recombinant > 95% as determined by Tris-Bis PAGE,> 95% as determined by HPLC
产品编号 ABIN7275798
发货至: 中国
  • 抗原 See all TACSTD2 蛋白
    TACSTD2 (Tumor-Associated Calcium Signal Transducer 2 (TACSTD2))
    蛋白类型
    Recombinant
    宿主
    • 23
    • 10
    • 3
    • 2
    • 2
    • 1
    • 1
    大鼠
    资源
    • 25
    • 6
    • 4
    • 2
    • 2
    • 1
    • 1
    HEK-293 Cells
    标记
    This TACSTD2 protein is labelled with His tag.
    序列
    Gln25-Gly270
    纯度
    > 95% as determined by Tris-Bis PAGE,> 95% as determined by HPLC
    过滤
    0.22 μm filtered
    内毒素水平
    Less than 1EU per μg by the LAL method.
    Top Product
    Discover our top product TACSTD2 蛋白
  • 限制
    仅限研究用
  • 状态
    Lyophilized
    溶解方式
    Centrifuge tubes before opening. Reconstituting to a concentration more than 100 μg/mL is recommended (usually we use 1 mg/mL solution for lyophilization). Dissolve the lyophilized protein in distilled water.
    缓冲液
    Lyophilized from 0.22μm filtered solution in PBS ( pH 7.4). Normally 5 % trehalose is added as protectant before lyophilization.
    储存条件
    4 °C,-80 °C
    储存方法
    Reconstituted protein stable at -80°C for 12 months, 4°C for 1 week. Use a manual defrost freezer and avoid repeated freeze-thaw cycles.
    有效期
    12 months
  • 抗原
    TACSTD2 (Tumor-Associated Calcium Signal Transducer 2 (TACSTD2))
    别名
    TROP-2 (TACSTD2 产品)
    别名
    EGP-1 Protein, EGP1 Protein, GA733-1 Protein, GA7331 Protein, GP50 Protein, M1S1 Protein, TROP2 Protein, C80403 Protein, Ly97 Protein, Prp1 Protein, tumor associated calcium signal transducer 2 Protein, tumor-associated calcium signal transducer 2 Protein, TACSTD2 Protein, Tacstd2 Protein
    背景
    EGP1, EGP-1, TROP2, GA733-1, gp50, T16, TACSTD2, TROP-2, M1S1, TACD2,Trop-2,also known as epithelial glycoprotein-1 antigen (EGP-1),is a protein that in humans is encoded by the TACSTD2 gene.Mutations of this gene result in gelatinous drop-like corneal dystrophy, an autosomal recessive disorder characterized by severe corneal amyloidosis leading to blindness.
    分子量
    28.9 kDa. Due to glycosylation, the protein migrates to 40-50 kDa based on Tris-Bis PAGE result.
    UniProt
    Q6P9Z6
You are here: