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Versican antibody

The Rabbit Monoclonal anti-Versican antibody has been validated for WB, IHC and IF. It is suitable to detect Versican in samples from Human.
Catalog No. ABIN7271309

Quick Overview for Versican antibody (ABIN7271309)

Target

See all Versican (Vcan) Antibodies
Versican (Vcan)

Reactivity

  • 51
  • 47
  • 27
  • 4
  • 1
  • 1
  • 1
Human

Host

  • 56
  • 24
  • 1
  • 1
Rabbit

Clonality

  • 51
  • 31
Monoclonal

Conjugate

  • 39
  • 4
  • 3
  • 3
  • 3
  • 3
  • 3
  • 3
  • 2
  • 2
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
This Versican antibody is un-conjugated

Application

  • 41
  • 24
  • 19
  • 16
  • 13
  • 13
  • 13
  • 9
  • 7
  • 3
  • 1
  • 1
  • 1
Western Blotting (WB), Immunohistochemistry (IHC), Immunofluorescence (IF)
  • Purpose

    Versican Rabbit mAb

    Cross-Reactivity

    Human, Mouse, Rat

    Characteristics

    Monoclonal Antibodies

    Purification

    Affinity purification

    Immunogen

    A synthesized peptide derived from human Versican

    Isotype

    IgG
  • Application Notes

    WB,1:500 - 1:2000,IHC,1:50 - 1:200,IF,1:50 - 1:200

    Restrictions

    For Research Use only
  • Format

    Liquid

    Buffer

    PBS with 0.02 % sodium azide,0.05 % BSA,50 % glycerol, pH 7.3.

    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 -20°C. Avoid freeze / thaw cycles.
  • Target

    Versican (Vcan)

    Alternative Name

    VCAN

    Background

    This gene is a member of the aggrecan/versican proteoglycan family. The protein encoded is a large chondroitin sulfate proteoglycan and is a major component of the extracellular matrix. This protein is involved in cell adhesion, proliferation, proliferation, migration and angiogenesis and plays a central role in tissue morphogenesis and maintenance. Mutations in this gene are the cause of Wagner syndrome type 1. Multiple transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Aug 2009],CSPG2, ERVR, GHAP, PG-M, WGN, WGN1,Cell Biology & Developmental Biology,Cytoskeleton,Extracellular Matrix,Signal Transduction,VCAN

    Molecular Weight

    373kDa

    Gene ID

    1462

    UniProt

    P13611

    Pathways

    Glycosaminoglycan Metabolic Process
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