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SCRN2 抗体

SCRN2 适用: 人, 小鼠, 大鼠 WB, IHC, ELISA 宿主: 兔 Polyclonal unconjugated
产品编号 ABIN7246619
发货至: 中国
  • 抗原 See all SCRN2 抗体
    SCRN2 (Secernin 2 (SCRN2))
    适用
    • 17
    • 13
    • 13
    • 2
    • 2
    • 2
    • 2
    • 2
    • 1
    • 1
    • 1
    • 1
    • 1
    人, 小鼠, 大鼠
    宿主
    • 15
    • 2
    克隆类型
    • 17
    多克隆
    标记
    • 10
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    This SCRN2 antibody is un-conjugated
    应用范围
    • 10
    • 4
    • 3
    • 2
    • 2
    • 2
    • 1
    • 1
    Western Blotting (WB), Immunohistochemistry (IHC), ELISA
    产品特性
    Polyclonal Antibody
    纯化方法
    Antigen affinity purification
    免疫原
    Fusion protein of human SCRN2
    亚型
    IgG
    Top Product
    Discover our top product SCRN2 Primary Antibody
  • 应用备注
    WB 1:500-1:2000, IHC 1:50-1:300, ELISA 1:5000-1:10000
    限制
    仅限研究用
  • 状态
    Liquid
    浓度
    1.08 mg/mL
    缓冲液
    PBS with 0.05 % Sodium azide and 40 % Glycerol, pH 7.4
    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
    Store at -20°C. Avoid freeze / thaw cycles.
  • 抗原
    SCRN2 (Secernin 2 (SCRN2))
    别名
    SCRN2 (SCRN2 产品)
    别名
    MGC147610 antibody, si:ch211-184m19.2 antibody, Ses2 antibody, AV001119 antibody, D11Moh48 antibody, SES2 antibody, secernin 2 antibody, secernin 2 S homeolog antibody, SCRN2 antibody, scrn2 antibody, scrn2.S antibody, Scrn2 antibody
    背景
    The SCRN (Secernin) gene family has three vertebrate paralogs, i.e. SCRN1, SCRN2 and SCRN3, which are closely linked to human HOXA, HOXB and HOXD cluster, respectively. SCRN2 (secernin-2) is a 425 amino acid protein that belongs to the peptidase C69 family and the Secernin subfamily. Vertebrate SCRN genes showed a topology of the form (A)(BC), i.e. (Hsa2 Hsa7)(Hsa17), with SCRN2 falling outside the SCRN3-SCRN1 cluster. The SCRN2 gene is conserved in dog, cow, mouse, rat and zebrafish, and maps to human chromosome 17q21.32. Chromosome 17 makes up over 2.5 % of the human genome with about 81 million bases encoding over 1,200 genes. Chromosome 17 is linked to neurofibromatosis, a condition characterized by neural and epidermal lesions, and dysregulated Schwann cell growth. Alexander disease, Birt-Hogg-Dube syndrome and Canavan disease are also associated with chromosome 17.
    分子量

    Observed_MW: Refer to figures

    Calculated_MW: 47 kDa

    UniProt
    Q96FV2
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