TMEM67 Antikörper (C-Term)

Produktnummer ABIN5517188

Der Kaninchen Polyklonal anti-TMEM67 Antikörper (ABIN5517188) detektiert spezifisch TMEM67 in WB. Dieser Antikörper reagiert spezifisch mit Proben aus Human.

Kurzübersicht für TMEM67 Antikörper (C-Term) (ABIN5517188)

Target: TMEM67 (Transmembrane Protein 67 (TMEM67))

Reaktivität: Human

Wirt: Kaninchen

Klonalität: Polyklonal

Konjugat: Dieser TMEM67 Antikörper ist unkonjugiert

Applikation: Western Blotting (WB)

Produktdetails anti-TMEM67 Antikörper

Bindungsspezifität: C-Term

Verwendungszweck: TMEM67 Antibody - C-terminal region

Sequenz: FDLLFFCVVD LACQNFILAS FLTYLQQEIF RYIRNTVGQK NLASKTLVDQ

Aufreinigung: Affinity purified

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

Anwendungsinformationen

Applikationshinweise: Optimal working dilution should be determined by the investigator.

Kommentare:

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

Beschränkungen: Nur für Forschungszwecke einsetzbar

Handhabung

Format: Liquid

Konzentration: 0.5 mg/mL

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

Konservierungsmittel: Sodium azide

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

Handhabung: prevent freeze-thaw cycles

Lagerung: 4 °C,-20 °C

Informationen zur Lagerung: 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.

Details zu TMEM67

Target: TMEM67 (Transmembrane Protein 67 (TMEM67))

Andere Bezeichnung: TMEM67

Hintergrund:

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

Molekulargewicht: 109 kDa

Gen-ID: 91147

NCBI Accession: NP_001135773

UniProt: Q5HYA8