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CD59 antibody

The Rabbit Polyclonal anti-CD59 antibody has been validated for IHC. It is suitable to detect CD59 in samples from Human, Mouse and Rat.
Catalog No. ABIN7259438

Quick Overview for CD59 antibody (ABIN7259438)

Target

See all CD59 Antibodies
CD59

Reactivity

  • 170
  • 16
  • 13
  • 10
  • 5
  • 5
  • 5
  • 1
  • 1
Human, Mouse, Rat

Host

  • 106
  • 95
  • 8
  • 6
Rabbit

Clonality

  • 118
  • 94
  • 1
Polyclonal

Conjugate

  • 106
  • 26
  • 14
  • 13
  • 8
  • 4
  • 3
  • 3
  • 3
  • 3
  • 3
  • 3
  • 3
  • 2
  • 2
  • 2
  • 2
  • 2
  • 2
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
This CD59 antibody is un-conjugated

Application

  • 107
  • 97
  • 85
  • 48
  • 46
  • 41
  • 33
  • 24
  • 16
  • 14
  • 13
  • 13
  • 11
  • 11
  • 11
  • 8
  • 3
  • 3
  • 3
  • 1
  • 1
  • 1
Immunohistochemistry (IHC)
  • Characteristics

    Polyclonal Antibody

    Purification

    Affinity purification

    Immunogen

    Recombinant protein of human CD59

    Isotype

    IgG
  • Application Notes

    IHC 1:50-1:200

    Restrictions

    For Research Use only
  • Format

    Liquid

    Concentration

    1 mg/mL

    Buffer

    PBS with 0.02 % sodium azide, 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

    CD59

    Alternative Name

    CD59

    Background

    This gene encodes a cell surface glycoprotein that regulates complement-mediated cell lysis, and it is involved in lymphocyte signal transduction. This protein is a potent inhibitor of the complement membrane attack complex, whereby it binds complement C8 and/or C9 during the assembly of this complex, thereby inhibiting the incorporation of multiple copies of C9 into the complex, which is necessary for osmolytic pore formation. This protein also plays a role in signal transduction pathways in the activation of T cells. Mutations in this gene cause CD59 deficiency, a disease resulting in hemolytic anemia and thrombosis, and which causes cerebral infarction. Multiple alternatively spliced transcript variants, which encode the same protein, have been identified for this gene.

    Gene ID

    966

    UniProt

    P13987

    Pathways

    Complement System
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