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NETO2 抗体 (PE)

This 兔 多克隆 antibody specifically detects NETO2 in FACS. It exhibits reactivity toward 人, 小鼠 和 大鼠.
产品编号 ABIN1428730
发货至: 中国
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Quick Overview for NETO2 抗体 (PE) (ABIN1428730)

抗原

See all NETO2 抗体
NETO2 (Neuropilin (NRP) and Tolloid (TLL)-Like 2 (NETO2))

适用

  • 43
  • 8
  • 8
  • 4
  • 4
  • 4
  • 3
  • 2
  • 2
  • 2
  • 1
  • 1
人, 小鼠, 大鼠

宿主

  • 40
  • 4

克隆类型

  • 42
  • 2
多克隆

标记

  • 20
  • 4
  • 3
  • 3
  • 2
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
This NETO2 antibody is conjugated to PE

应用范围

  • 25
  • 21
  • 13
  • 13
  • 11
  • 10
  • 4
  • 3
  • 3
  • 1
  • 1
Flow Cytometry (FACS)
  • 纯化方法

    Purified by Protein A.

    免疫原

    KLH conjugated synthetic peptide derived from human NETO2

    亚型

    IgG
  • 应用备注

    FCM(1:20-100)

    说明

    Exitation/Emission: 480,565nm/578nm

    限制

    仅限研究用
  • 状态

    Liquid

    浓度

    1 μg/μL

    缓冲液

    Aqueous buffered solution containing 1 % BSA, 50 % glycerol and 0.09 % sodium azide.

    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 4°C

    有效期

    12 months
  • 抗原

    NETO2 (Neuropilin (NRP) and Tolloid (TLL)-Like 2 (NETO2))

    别名

    Neto2

    背景

    NETO2 is a 525 amino acid single-pass type I membrane protein that contains two CUB domains and one LDL-receptor class A domain. Expressed as multiple alternatively spliced isoforms, NETO2 is thought to play a role in the development and maintenance of neuronal circuitry, possibly playing a role in proper brain function. The gene encoding NETO2 maps to human chromosome 16, which is associated with a variety of genetic disorders, encodes over 900 genes and comprises nearly 3 % of the human genome. The GAN gene is located on chromosome 16 and, with mutation, may lead to giant axonal neuropathy, a nervous system disorder characterized by increasing malfunction with growth. The rare disorder Rubinstein-Taybi syndrome is associated with chromosome 16, as is Crohn's disease, which is a gastrointestinal inflammatory condition.

    Subcellular location: Extracellular


    Synonyms: Brain specic transmembrane protein, Brain specic transmembrane protein containing 2 CUB and 1 LDL receptor class A domains protein 2, Brain-specic transmembrane protein containing 2 CUB and 1 LDL-receptor class A domains protein 2, BTCL2, FLJ10430, FLJ14724, FLJ90456, NEOT2, NETO 2, Neto2, NETO2_HUMAN, Neuropilin NRP and tolloid TLL like 2, Neuropilin and tolloid like protein 2, Neuropilin and tolloid-like protein 2.
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