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Fibulin 5 抗体

FBLN5 适用: 人, 小鼠 WB, IF 宿主: 兔 Polyclonal unconjugated
产品编号 ABIN6572097
发货至: 中国
  • 抗原 See all Fibulin 5 (FBLN5) 抗体
    Fibulin 5 (FBLN5)
    适用
    • 53
    • 30
    • 23
    • 1
    人, 小鼠
    宿主
    • 52
    • 6
    • 1
    克隆类型
    • 53
    • 8
    多克隆
    标记
    • 28
    • 8
    • 6
    • 4
    • 2
    • 2
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    This Fibulin 5 antibody is un-conjugated
    应用范围
    • 56
    • 32
    • 15
    • 5
    • 4
    • 3
    • 3
    • 1
    Western Blotting (WB), Immunofluorescence (IF)
    纯化方法
    Affinity purification
    免疫原
    Recombinant fusion protein of human FBLN5 (NP_006320.2).
    亚型
    IgG
    Top Product
    Discover our top product FBLN5 Primary Antibody
  • 应用备注
    WB 1:500-1:2000 IF 1:50-1:100
    限制
    仅限研究用
  • 状态
    Liquid
    浓度
    1 mg/mL
    缓冲液
    PBS with 0.02 % sodium azide, 50 % glycerol, pH 7.3
    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
    Fibulin 5 (FBLN5)
    别名
    FBLN5 (FBLN5 产品)
    别名
    zgc:103575 antibody, FBLN5 antibody, MGC108414 antibody, Fibulin-5 antibody, DKFZp469K0327 antibody, ADCL2 antibody, ARCL1A antibody, ARMD3 antibody, DANCE antibody, EVEC antibody, FIBL-5 antibody, UP50 antibody, A55 antibody, fibulin 5 antibody, fbln5 antibody, FBLN5 antibody, Fbln5 antibody
    背景
    The protein encoded by this gene is a secreted, extracellular matrix protein containing an Arg-Gly-Asp (RGD) motif and calcium-binding EGF-like domains. It promotes adhesion of endothelial cells through interaction of integrins and the RGD motif. It is prominently expressed in developing arteries but less so in adult vessels. However, its expression is reinduced in balloon-injured vessels and atherosclerotic lesions, notably in intimal vascular smooth muscle cells and endothelial cells. Therefore, the protein encoded by this gene may play a role in vascular development and remodeling. Defects in this gene are a cause of autosomal dominant cutis laxa, autosomal recessive cutis laxa type I (CL type I), and age-related macular degeneration type 3 (ARMD3).
    分子量

    Observed_MW: 70kDa

    Calculated_MW: 50kDa

    基因ID
    10516
    UniProt
    Q9UBX5
    途径
    SARS-CoV-2 Protein Interactome
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