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

ECM1 Protein (Transcript Variant 1) (Myc-DYKDDDDK Tag)

ECM1 宿主: 人 宿主: HEK-293 Cells Recombinant > 80 % as determined by SDS-PAGE and Coomassie blue staining AbP, STD
产品编号 ABIN2731598
发货至: 中国
  • 抗原 See all ECM1 蛋白
    ECM1 (Extracellular Matrix Protein 1 (ECM1))
    蛋白类型
    Recombinant
    产品特性
    Transcript Variant 1
    宿主
    • 5
    • 4
    • 1
    • 1
    资源
    • 5
    • 2
    • 2
    • 1
    • 1
    HEK-293 Cells
    标记
    This ECM1 protein is labelled with Myc-DYKDDDDK Tag.
    应用范围
    Antibody Production (AbP), Standard (STD)
    产品特性
    • Recombinant human Secretory component / ECM1 (transcript variant 1) protein expressed in HEK293 cells.
    • Produced with end-sequenced ORF clone
    纯度
    > 80 % as determined by SDS-PAGE and Coomassie blue staining
    Top Product
    Discover our top product ECM1 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 C-terminal.

    限制
    仅限研究用
  • 浓度
    50 μg/mL
    缓冲液
    25 mM Tris.HCl, pH 7.3, 100 mM glycine, 10 % glycerol.
    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
    ECM1 (Extracellular Matrix Protein 1 (ECM1))
    别名
    Secretory Component,ecm1 (ECM1 产品)
    别名
    URBWD Protein, ECM Protein, EMILIN4 Protein, GPIa* Protein, MMRN Protein, AI663821 Protein, p85 Protein, extracellular matrix protein 1 Protein, multimerin 1 Protein, ECM1 Protein, MMRN1 Protein, Ecm1 Protein
    背景
    This gene encodes a soluble protein that is involved in endochondral bone formation, angiogenesis, and tumor biology. It also interacts with a variety of extracellular and structural proteins, contributing to the maintenance of skin integrity and homeostasis. Mutations in this gene are associated with lipoid proteinosis disorder (also known as hyalinosis cutis et mucosae or Urbach-Wiethe disease) that is characterized by generalized thickening of skin, mucosae and certain viscera. Alternatively spliced transcript variants encoding distinct isoforms have been described for this gene.
    分子量
    58.8 kDa
    NCBI登录号
    NP_004416
You are here:
客服