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LOXL1 抗体

This anti-LOXL1 antibody is a 兔 多克隆 antibody detecting LOXL1 in WB 和 ELISA. Suitable for 人, 小鼠 和 大鼠.
产品编号 ABIN7115988
发货至: 中国

Quick Overview for LOXL1 抗体 (ABIN7115988)

抗原

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

适用

  • 48
  • 18
  • 7
  • 4
  • 4
  • 3
  • 3
  • 2
  • 2
  • 1
人, 小鼠, 大鼠

宿主

  • 49
  • 6

克隆类型

  • 51
  • 4
多克隆

标记

  • 26
  • 10
  • 9
  • 4
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
This LOXL1 antibody is un-conjugated

应用范围

  • 35
  • 17
  • 15
  • 9
  • 8
  • 8
  • 3
  • 1
  • 1
Western Blotting (WB), ELISA
  • 纯化方法

    Immunogen affinity purified

    纯度

    ≥95 % as determined by SDS-PAGE

    免疫原

    lysyl oxidase-like 1

    亚型

    IgG
  • 应用备注

    WB: 1:500 - 1:2000

    限制

    仅限研究用
  • 状态

    Liquid

    缓冲液

    PBS with 0.02 % sodium azide and 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

    -20°C for 12 months (Avoid repeated freeze / thaw cycles.)

    有效期

    12 months
  • 抗原

    LOXL1 (Lysyl Oxidase-Like 1 (LOXL1))

    别名

    LOXL1

    背景

    Synonyms:LOL, LOXL, LOXL1, Lysyl oxidase homolog 1, lysyl oxidase like 1, Lysyl oxidase like protein 1 Background: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

    70kDa

    基因ID

    4016

    UniProt

    Q08397
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