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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
-15% Promotion 2026
$407.74
$479.69
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100 μL
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Quick Overview for NETO2 antibody (PE) (ABIN1428730)

Target

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

Reactivity

  • 43
  • 8
  • 8
  • 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
  • 11
  • 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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