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CLDND2 antibody

The Rabbit Polyclonal anti-CLDND2 antibody has been validated for ELISA and IHC. It is suitable to detect CLDND2 in samples from Human and Mouse.
Catalog No. ABIN7244468

Quick Overview for CLDND2 antibody (ABIN7244468)

Target

See all CLDND2 Antibodies
CLDND2 (Claudin Domain Containing 2 (CLDND2))

Reactivity

Human, Mouse

Host

  • 9
  • 2
Rabbit

Clonality

  • 11
Polyclonal

Conjugate

  • 4
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
This CLDND2 antibody is un-conjugated

Application

  • 4
  • 2
  • 2
ELISA, Immunohistochemistry (IHC)
  • Characteristics

    Polyclonal Antibody

    Purification

    Affinity purification

    Immunogen

    Synthetic peptide of human CLDND2

    Isotype

    IgG
  • Application Notes

    IHC 1:30-150, ELISA 1:2000-10000

    Restrictions

    For Research Use only
  • Format

    Liquid

    Concentration

    1.4 mg/mL

    Buffer

    PBS with 0.05 % sodium azide and 50 % glycerol, PH7.4

    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

    CLDND2 (Claudin Domain Containing 2 (CLDND2))

    Alternative Name

    CLDND2

    Background

    CLDND2 (claudin domain containing 2) is a 167 amino acid multi-pass membrane protein that belongs to the PMP-22/EMP/MP20 family and is encoded by a gene that maps to human chromosome 19q13.33. Consisting of around 63 million bases with over 1,400 genes, chromosome 19 makes up over 2 % of human genomic DNA. Chromosome 19 includes a diversity of interesting genes and is recognized for having the greatest gene density of the human chromosomes. It is the genetic home for a number of immunoglobulin superfamily members including the killer cell and leukocyte Ig-like receptors, a number of ICAMs, the CEACAM and PSG family, and Fc receptors. Key genes for eye color and hair color also map to chromosome 19. Peutz-Jeghers syndrome, spinocerebellar ataxia type 6, the stroke disorder CADASIL, hypercholesterolemia and insulin-dependent diabetes have been linked to chromosome 19.

    NCBI Accession

    NP_689566

    UniProt

    Q8NHS1
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