PDZD7 anticorps (Biotin)

N° du produit ABIN1400503

Détail du produit anti-PDZD7 anticorps (Biotin)

Antigène: PDZD7 (PDZ Domain Containing 7 (PDZD7))

Reactivité: Humain, Souris, Rat

Hôte: Lapin

Clonalité: Polyclonal

Conjugué: Cet anticorp PDZD7 est conjugé à/à la Biotin

Application: Western Blotting (WB), Immunohistochemistry (Paraffin-embedded Sections) (IHC (p))

Réactivité croisée: Humain, Souris, Rat

Purification: Purified by Protein A.

Immunogène: KLH conjugated synthetic peptide derived from human PDZD7

Isotype: IgG

Information d'application

Indications d'application: WB 1:300-5000
IHC-P 1:200-400

Restrictions: For Research Use only

Stockage

Format: Liquid

Concentration: 1 μg/μL

Buffer: Aqueous buffered solution containing 0.01M TBS ( pH 7.4) with 1 % BSA, 0.03 % Proclin300 and 50 % Glycerol.

Agent conservateur: ProClin

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

Stock: -20 °C

Stockage commentaire: Store at -20°C for 12 months.

Date de péremption: 12 months

Détails sur PDZD7

Antigène: PDZD7 (PDZ Domain Containing 7 (PDZD7))

Autre désignation: PDZD7 (PDZD7 Produits)

Synonymes: anticorps PDZK7, anticorps Pdzk7, anticorps PDZD7, anticorps DKFZp459K1926, anticorps si:dkey-158p2.1, anticorps 9130207N01, anticorps EG435601, anticorps PDZ domain containing 7, anticorps PDZ domain containing 7a, anticorps PDZD7, anticorps Pdzd7, anticorps pdzd7a

Sujet:

Synonyms: PDZ domain containing 7, PDZK7, RP11-108L7.9, EG435601, OTTMUSP00000044305, 9130207N01, OTTMUSP00000044304, PDZD7_HUMAN.

Background: PDZK7, also known as PDZD7, is a 517 amino acid protein that contains two PDZ (DHR) domains. Encoded by a gene that maps to human chromosome 10q24.31, PDZK7 is conserved in dog, mouse and rat, and exists as three alternatively spliced isoforms. PDZK7 is known to interact with Harmonin, MASS1, USH1G and Usherin. Localizing to nucleus, PDZK7 is expressed in retinal pigment epithelium and inner ear. Biallelic inactivation of PDZK7 can cause non-syndromic hearing impairment and chromosomal aberrations, which are linked to non-syndromic sensorineural deafness. PDZK7 mutations are also linked to Usher syndrome, which is characterized by retinitis pigmentosa and sensorineural deafness, and Alzheimer disease. The gene that encodes PDZK7 maps to human chromosome 10q24.31.

ID gène: 79955