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LOXL1 抗体

This 兔 多克隆 anti-LOXL1 antibody specifically detects LOXL1 in IF. The antibody is reactive with 人, 小鼠 和 大鼠 samples.
产品编号 ABIN7255189
发货至: 中国
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Tel +86 (0512) 65829739 传真 +86 (010) 6788 5057

Quick Overview for LOXL1 抗体 (ABIN7255189)

抗原

See all LOXL1 抗体
LOXL1 (Lysyl Oxidase-Like 1 (LOXL1))

适用

  • 49
  • 19
  • 8
  • 4
  • 4
  • 3
  • 3
  • 2
  • 2
  • 1
人, 小鼠, 大鼠

宿主

  • 50
  • 6

克隆类型

  • 52
  • 4
多克隆

标记

  • 27
  • 10
  • 9
  • 4
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
This LOXL1 antibody is un-conjugated

应用范围

  • 36
  • 18
  • 15
  • 9
  • 8
  • 7
  • 3
  • 1
  • 1
Immunofluorescence (IF)
  • 产品特性

    Polyclonal Antibody

    纯化方法

    Affinity purification

    免疫原

    Recombinant fusion protein of human LOXL1 (NP_005567.2).

    亚型

    IgG
  • 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

    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.

    基因ID

    4016

    UniProt

    Q08397
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