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CLDND2 antibody

The Rabbit Polyclonal anti-CLDND2 antibody is suitable to detect CLDND2 in samples from Human and Mouse. It has been validated for ELISA and IHC.
Catalog No. ABIN7244468
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$457.98
$538.80
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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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