CLDND2 anticorps

N° du produit ABIN7244468

L’anticorps Lapin Polyclonal anti-CLDND2 a été validé pour ELISA et IHC. Il convient pour détecter CLDND2 dans des échantillons de Humain et Souris.

Aperçu rapide pour CLDND2 anticorps (ABIN7244468)

Antigène: CLDND2 (Claudin Domain Containing 2 (CLDND2))

Reactivité: Humain, Souris

Hôte: Lapin

Clonalité: Polyclonal

Conjugué: Cet anticorp CLDND2 est non-conjugé

Application: ELISA, Immunohistochemistry (IHC)

Détail du produit anti-CLDND2 anticorps

Attributs du produit: Polyclonal Antibody

Purification: Affinity purification

Immunogène: Synthetic peptide of human CLDND2

Isotype: IgG

Information d'application

Indications d'application: IHC 1:30-150, ELISA 1:2000-10000

Restrictions: For Research Use only

Stockage

Format: Liquid

Concentration: 1.4 mg/mL

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

Agent conservateur: Sodium azide

Précaution d'utilisation: This product contains Sodium azide: a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.

Stock: -20 °C

Stockage commentaire: Store at -20°C. Avoid freeze / thaw cycles.

Détails sur CLDND2

Antigène: CLDND2 (Claudin Domain Containing 2 (CLDND2))

Autre désignation: CLDND2

Sujet: 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