TMEM67 anticorps (C-Term)

N° du produit ABIN5517188

Cet anticorps anti-TMEM67 Polyclonal Lapin (ABIN5517188) détecte spécifiquement TMEM67 dans WB. L’anticorps est réactif avec des échantillons de Humain.

Aperçu rapide pour TMEM67 anticorps (C-Term) (ABIN5517188)

Antigène: TMEM67 (Transmembrane Protein 67 (TMEM67))

Reactivité: Humain

Hôte: Lapin

Clonalité: Polyclonal

Conjugué: Cet anticorp TMEM67 est non-conjugé

Application: Western Blotting (WB)

Détail du produit anti-TMEM67 anticorps

Épitope: C-Term

Fonction: TMEM67 Antibody - C-terminal region

Séquence: FDLLFFCVVD LACQNFILAS FLTYLQQEIF RYIRNTVGQK NLASKTLVDQ

Purification: Affinity purified

Immunogène: The immunogen is a synthetic peptide directed towards the C terminal region of human TMEM67

Information d'application

Indications d'application: Optimal working dilution should be determined by the investigator.

Commentaires:

We also sell a specific blocking peptide that can be used in combination with this antibody. You can find the blocking peptide under AAP78321-100UG

Restrictions: For Research Use only

Stockage

Format: Liquid

Concentration: 0.5 mg/mL

Buffer: Purified antibody supplied in 1x PBS buffer with 0.09 % (w/v) sodium azide and 2 % sucrose.

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.

Conseil sur la manipulation: prevent freeze-thaw cycles

Stock: 4 °C,-20 °C

Stockage commentaire: For short term use, store at 2-8C up to 1 week. For long term storage, store at -20 °C in small aliquots to prevent freeze-thaw cycles.

Détails sur TMEM67

Antigène: TMEM67 (Transmembrane Protein 67 (TMEM67))

Autre désignation: TMEM67

Sujet:

Background Information: The protein encoded by this gene localizes to the primary cilium and to the plasma membrane. The gene functions in centriole migration to the apical membrane and formation of the primary cilium. Multiple transcript variants encoding different isoforms have been found for this gene. Defects in this gene are a cause of Meckel syndrome type 3 (MKS3) and Joubert syndrome type 6 (JBTS6).

Gene Name: transmembrane protein 67

Alternative Symbols: MKS3, JBTS6, NPHP11, TNEM67, MECKELIN

Protein Name: meckelin

Poids moléculaire: 109 kDa

ID gène: 91147

NCBI Accession: NP_001135773

UniProt: Q5HYA8