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LOXL1 抗体

LOXL1 适用: 人, 小鼠, 大鼠 IF 宿主: 兔 Polyclonal unconjugated
产品编号 ABIN6566806
发货至: 中国
  • 抗原 See all LOXL1 抗体
    LOXL1 (Lysyl Oxidase-Like 1 (LOXL1))
    适用
    • 48
    • 22
    • 8
    • 4
    • 4
    • 3
    • 3
    • 2
    • 2
    • 1
    人, 小鼠, 大鼠
    宿主
    • 53
    • 6
    克隆类型
    • 55
    • 4
    多克隆
    标记
    • 27
    • 11
    • 10
    • 5
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    This LOXL1 antibody is un-conjugated
    应用范围
    • 35
    • 22
    • 13
    • 10
    • 9
    • 8
    • 3
    • 2
    • 1
    • 1
    • 1
    Immunofluorescence (IF)
    纯化方法
    Affinity purification
    免疫原
    Recombinant fusion protein of human LOXL1 (NP_005567.2).
    亚型
    IgG
    Top Product
    Discover our top product LOXL1 Primary Antibody
  • 应用备注
    IF 1:50-1:200
    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
    LOXL1 (Lysyl Oxidase-Like 1 (LOXL1))
    别名
    LOXL1 (LOXL1 产品)
    别名
    LOL antibody, LOXL antibody, Loxl antibody, si:ch211-238c15.1 antibody, lol antibody, loxl antibody, loxl-1 antibody, oxl-1 antibody, lysyl oxidase like 1 antibody, lysyl oxidase-like 1 antibody, lysyl oxidase like 1 L homeolog antibody, LOXL1 antibody, loxl1 antibody, Loxl1 antibody, loxl1.L antibody
    背景
    This gene encodes a member of the lysyl oxidase family of proteins. The prototypic member of the family is essential to the biogenesis of connective tissue, encoding an extracellular copper-dependent amine oxidase that catalyzes the first step in the formation of crosslinks in collagen and elastin. The encoded preproprotein is proteolytically processed to generate the mature enzyme. A highly conserved amino acid sequence at the C-terminus end appears to be sufficient for amine oxidase activity, suggesting that each family member may retain this function. The N-terminus is poorly conserved and may impart additional roles in developmental regulation, senescence, tumor suppression, cell growth control, and chemotaxis to each member of the family. Mutations in this gene are associated with exfoliation syndrome.
    分子量

    Observed_MW: 80kDa

    Calculated_MW: 63kDa

    基因ID
    4016
    UniProt
    Q08397
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