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CISD2 antibody (AA 55-124)

This Rabbit Polyclonal antibody specifically detects CISD2 in WB, ELISA, IF, IHC (p) and FACS. It exhibits reactivity toward Human, Mouse and Rat.
Catalog No. ABIN7875671
$625.62
Plus shipping costs $50.00
100 μg
Shipping to: United States
Delivery in 2 to 4 Business Days

Quick Overview for CISD2 antibody (AA 55-124) (ABIN7875671)

Target

See all CISD2 Antibodies
CISD2 (CDGSH Iron Sulfur Domain 2 (CISD2))

Reactivity

  • 17
  • 10
  • 5
  • 3
  • 2
  • 2
  • 2
  • 2
  • 2
  • 1
  • 1
  • 1
Human, Mouse, Rat

Host

  • 18
  • 3
Rabbit

Clonality

  • 18
  • 3
Polyclonal

Conjugate

  • 17
  • 2
  • 1
  • 1
This CISD2 antibody is un-conjugated

Application

  • 17
  • 13
  • 6
  • 5
  • 2
  • 1
  • 1
  • 1
  • 1
Western Blotting (WB), ELISA, Immunofluorescence (IF), Immunohistochemistry (Paraffin-embedded Sections) (IHC (p)), Flow Cytometry (FACS)
  • Binding Specificity

    • 6
    • 3
    • 2
    • 2
    • 1
    • 1
    • 1
    AA 55-124

    Purpose

    NAF-1 Antibody / CISD2 / Miner1

    Purification

    Affinity purified

    Immunogen

    Recombinant human protein (amino acids A55-N124) was used as the immunogen for the NAF-1 antibody.

    Isotype

    IgG
  • Application Notes

    Optimal dilution of the NAF-1 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 NAF-1 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

    CISD2 (CDGSH Iron Sulfur Domain 2 (CISD2))

    Alternative Name

    NAF-1

    Background

    CDGSH iron sulfur domain 2 is a protein that in humans is encoded by the CISD2 gene. The protein encoded by this gene is a zinc finger protein that localizes to the endoplasmic reticulum. The encoded protein binds an iron/sulfur cluster and may be involved in calcium homeostasis. Defects in this gene are a cause of Wolfram syndrome 2.

    UniProt

    Q8N5K1

    Pathways

    Activation of Innate immune Response
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