CLDN14 anticorps (AA 177-189)

N° du produit ABIN1886114

L’anticorps Lapin Polyclonal anti-CLDN14 a été validé pour WB. Il convient pour détecter CLDN14 dans des échantillons de Humain.

Aperçu rapide pour CLDN14 anticorps (AA 177-189) (ABIN1886114)

Antigène: CLDN14 (Claudin 14 (CLDN14))

Reactivité: Humain

Hôte: Lapin

Clonalité: Polyclonal

Conjugué: Cet anticorp CLDN14 est non-conjugé

Application: Western Blotting (WB)

Détail du produit anti-CLDN14 anticorps

Épitope: AA 177-189

Purification: Purified by antigen-affinity chromatography.

Immunogène: Synthetic peptide contain a sequence corresponding to a region within amino acids 177 and 189 (O95500) of Claudin 14

Information d'application

Indications d'application: Suggested dilutions:
Western blotting: 1.500-1.3000

Restrictions: For Research Use only

Stockage

Format: Liquid

Buffer: 1 x PBS, 40 % Glycerol (pH 7.0).0.01 % Thimerosal was added as a preservative.

Agent conservateur: Thimerosal (Merthiolate)

Précaution d'utilisation: Biohazard Informations: This product contains thimerosal which is hazardous.

Stock: 4 °C/-20 °C

Stockage commentaire: Store at -20 °C for long term preservation (recommended). Store at 4 °C for short term use.

Détails sur CLDN14

Antigène: CLDN14 (Claudin 14 (CLDN14))

Autre désignation: claudin 14

Sujet: Tight junctions represent one mode of cell-to-cell adhesion in epithelial or endothelial cell sheets, forming continuous seals around cells and serving as a physical barrier to prevent solutes and water from passing freely through the paracellular space.These junctions are comprised of sets of continuous networking strands in the outwardly facing cytoplasmic leaflet, with complementary grooves in the inwardly facing extracytoplasmic leaflet.The protein encoded by this gene, a member of the claudin family, is an integral membrane protein and a component of tight junction strands.The encoded protein also binds specifically to the WW domain of Yes-associated protein.Defects in this gene are the cause of an autosomal recessive form of nonsyndromic sensorineural deafness.Several transcript variants encoding the same protein have been found for this gene.[provided by RefSeq]

Poids moléculaire: 26 kDa

ID gène: 23562

NCBI Accession: NM_012130, NP_036262

Pathways: Cell-Cell Junction Organization, Hepatitis C