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NETO2 antibody (PE)

This Rabbit Polyclonal antibody specifically detects NETO2 in FACS. It exhibits reactivity toward Human, Mouse and Rat.
Catalog No. ABIN1428730

Quick Overview for NETO2 antibody (PE) (ABIN1428730)

Target

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

Reactivity

  • 43
  • 7
  • 7
  • 4
  • 4
  • 4
  • 3
  • 2
  • 2
  • 2
  • 1
  • 1
Human, Mouse, Rat

Host

  • 40
  • 4
Rabbit

Clonality

  • 42
  • 2
Polyclonal

Conjugate

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

Application

  • 25
  • 21
  • 13
  • 13
  • 12
  • 10
  • 4
  • 3
  • 3
  • 1
  • 1
Flow Cytometry (FACS)
  • Purification

    Purified by Protein A.

    Immunogen

    KLH conjugated synthetic peptide derived from human NETO2

    Isotype

    IgG
  • Application Notes

    FCM(1:20-100)

    Comment

    Exitation/Emission: 480,565nm/578nm

    Restrictions

    For Research Use only
  • Format

    Liquid

    Concentration

    1 μg/μL

    Buffer

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

    Preservative

    Sodium azide

    Precaution of Use

    This product contains Sodium azide: a POISONOUS AND HAZARDOUS SUBSTANCE, which should be handled by trained staff only.

    Storage

    -20 °C

    Storage Comment

    Store at 4°C

    Expiry Date

    12 months
  • Target

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

    Alternative Name

    Neto2

    Background

    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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