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FANCD2 antibody

This Rabbit Monoclonal antibody specifically detects FANCD2 in WB. It exhibits reactivity toward Human.
Catalog No. ABIN7267126

Quick Overview for FANCD2 antibody (ABIN7267126)

Target

See all FANCD2 Antibodies
FANCD2 (Fanconi Anemia, Complementation Group D2 (FANCD2))

Reactivity

  • 68
  • 25
  • 22
  • 1
  • 1
  • 1
  • 1
Human

Host

  • 68
  • 1
Rabbit

Clonality

  • 59
  • 10
Monoclonal

Conjugate

  • 29
  • 5
  • 3
  • 3
  • 3
  • 3
  • 3
  • 3
  • 3
  • 2
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
This FANCD2 antibody is un-conjugated

Application

  • 25
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  • 19
  • 14
  • 14
  • 14
  • 7
  • 7
  • 7
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  • 4
  • 1
  • 1
Western Blotting (WB)
  • Purpose

    FANCD2 Rabbit mAb

    Cross-Reactivity

    Human, Mouse, Rat

    Characteristics

    Monoclonal Antibodies

    Purification

    Affinity purification

    Immunogen

    A synthesized peptide derived from human FANCD2.

    Isotype

    IgG
  • Application Notes

    WB,1:500 - 1:2000

    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

    FANCD2 (Fanconi Anemia, Complementation Group D2 (FANCD2))

    Alternative Name

    FANCD2

    Background

    The Fanconi anemia complementation group (FANC) currently includes FANCA, FANCB, FANCC, FANCD1 (also called BRCA2), FANCD2, FANCE, FANCF, FANCG, FANCI, FANCJ (also called BRIP1), FANCL, FANCM and FANCN (also called PALB2). The previously defined group FANCH is the same as FANCA. Fanconi anemia is a genetically heterogeneous recessive disorder characterized by cytogenetic instability, hypersensitivity to DNA crosslinking agents, increased chromosomal breakage, and defective DNA repair. The members of the Fanconi anemia complementation group do not share sequence similarity, they are related by their assembly into a common nuclear protein complex. This gene encodes the protein for complementation group D2. This protein is monoubiquinated in response to DNA damage, resulting in its localization to nuclear foci with other proteins (BRCA1 AND BRCA2) involved in homology-directed DNA repair. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Feb 2016],FA4,FAD,FACD,FAD2,FA-D2,FANCD,FANCD2,Cell Biology & Developmental Biology,Cell Cycle,DNA Damage & Repair,Epigenetics & Nuclear Signaling,G2/M DNA Damage Checkpoint,FANCD2

    Molecular Weight

    166kDa

    Gene ID

    2177

    UniProt

    Q9BXW9

    Pathways

    DNA Damage Repair
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