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DPYSL2 antibody

The Rabbit Polyclonal anti-DPYSL2 antibody (ABIN7880629) specifically detects DPYSL2 in WB and IF. The antibody is reactive with Human, Mouse and Rat samples.
Catalog No. ABIN7880629
$625.62
Plus shipping costs $50.00
100 μg
Shipping to: United States
Delivery in 2 to 4 Business Days

Quick Overview for DPYSL2 antibody (ABIN7880629)

Target

See all DPYSL2 Antibodies
DPYSL2 (Dihydropyrimidinase-Like 2 (DPYSL2))

Reactivity

  • 138
  • 98
  • 91
  • 3
  • 2
  • 2
  • 2
  • 2
  • 2
  • 2
  • 1
  • 1
  • 1
  • 1
Human, Mouse, Rat

Host

  • 136
  • 4
Rabbit

Clonality

  • 116
  • 24
Polyclonal

Conjugate

  • 51
  • 7
  • 6
  • 6
  • 6
  • 6
  • 6
  • 6
  • 6
  • 4
  • 3
  • 3
  • 3
  • 3
  • 3
  • 3
  • 3
  • 3
  • 3
  • 3
  • 3
  • 1
  • 1
  • 1
This DPYSL2 antibody is un-conjugated

Application

  • 84
  • 40
  • 39
  • 39
  • 35
  • 27
  • 27
  • 15
  • 14
  • 13
  • 9
  • 1
  • 1
Western Blotting (WB), Immunofluorescence (IF)
  • Purpose

    CRMP2 Antibody / DPYSL2

    Purification

    Antigen affinity purified

    Immunogen

    Amio acids KDRFQLTDCQIYEVLSV were used as the immunogen for the CRMP2 antibody.

    Isotype

    IgG
  • Application Notes

    Optimal dilution of the CRMP2 antibody should be determined by the researcher.

    Restrictions

    For Research Use only
  • Format

    Lyophilized

    Buffer

    0.5 mg/mL if reconstituted with 0.2 mL sterile DI water

    Storage

    4 °C,-20 °C

    Storage Comment

    After reconstitution, the CRMP2 antibody can be stored for up to one month at 4oC. For long-term, aliquot and store at -20oC. Avoid repeated freezing and thawing.
  • Target

    DPYSL2 (Dihydropyrimidinase-Like 2 (DPYSL2))

    Alternative Name

    CRMP2

    Background

    Dihydropyrimidinase-related protein 2, also called Collapsin response mediator protein 2 (CRMP2), is an enzyme that in humans is encoded by the DPYSL2 gene. This gene encodes a member of the collapsin response mediator protein family. Collapsin response mediator proteins form homo- and hetero-tetramers and facilitate neuron guidance, growth and polarity. The encoded protein promotes microtubule assembly and is required for Sema3A-mediated growth cone collapse, and also plays a role in synaptic signaling through interactions with calcium channels. This gene has been implicated in multiple neurological disorders, and hyperphosphorylation of the encoded protein may play a key role in the development of Alzheimer's disease. Alternatively spliced transcript variants encoding multiple isoforms have been observed for this gene.

    UniProt

    Q16555

    Pathways

    Regulation of Cell Size
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