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GP6 antibody (Biotin)

This Human Chimeric antibody specifically detects GP6 in FACS. It exhibits reactivity toward Human.
Catalog No. ABIN7608232
-15% Promotion 2026
$223.29
$262.70
save $39.41 (-15 %)
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10 μg
Shipping to: United States
Delivery in 20 to 21 Business Days

Quick Overview for GP6 antibody (Biotin) (ABIN7608232)

Target

See all GP6 Antibodies
GP6 (Glycoprotein VI (Platelet) (GP6))

Reactivity

  • 62
  • 21
  • 19
Human

Host

  • 56
  • 6
  • 1
Human, Rabbit

Clonality

  • 55
  • 7
  • 1
Chimeric

Conjugate

  • 20
  • 6
  • 6
  • 4
  • 3
  • 3
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
This GP6 antibody is conjugated to Biotin

Application

  • 44
  • 18
  • 13
  • 13
  • 8
  • 6
  • 3
  • 2
  • 2
  • 2
  • 2
  • 1
Flow Cytometry (FACS)

Clone

DMC427
  • Purpose

    Biotinylated Anti-GP6 antibody(DMC427), IgG1 Chimeric mAb

    Purification

    Purified from cell culture supernatant by affinity chromatography

    Isotype

    IgG1
  • Application Notes

    Flow Cyt 1:100

    Restrictions

    For Research Use only
  • Format

    Lyophilized

    Buffer

    Lyophilized from sterile PBS, pH 7.4. Normally 5 % - 8 % trehalose is added as protectants before lyophilization.

    Storage

    -20 °C,-80 °C

    Storage Comment

    Store at -20°C to -80°C for 12 months in lyophilized form. After reconstitution, if not intended for use within a month, aliquot and store at -80°C (Avoid repeated freezing and thawing). Lyophilized proteins are shipped at ambient temperature.

    Expiry Date

    12 months
  • Target

    GP6 (Glycoprotein VI (Platelet) (GP6))

    Alternative Name

    GP6

    Background

    This gene encodes a platelet membrane glycoprotein of the immunoglobulin superfamily. The encoded protein is a receptor for collagen and plays a critical role in collagen-induced platelet aggregation and thrombus formation. The encoded protein forms a complex with the Fc receptor gamma-chain that initiates the platelet activation signaling cascade upon collagen binding. Mutations in this gene are a cause of platelet-type bleeding disorder-11 (BDPLT11). Alternatively spliced transcript variants encoding multiple isoforms have been observed for this gene.

    UniProt

    Q9HCN6
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