IMMP2L Antikörper (AA 30-110)

Produktnummer ABIN7229132

Der Kaninchen Polyklonal anti-IMMP2L Antikörper (ABIN7229132) detektiert spezifisch IMMP2L in WB und ELISA. Dieser Antikörper reagiert spezifisch mit Proben aus Human und Maus.

Kurzübersicht für IMMP2L Antikörper (AA 30-110) (ABIN7229132)

Target: IMMP2L (Inner Mitochondrial Membrane Peptidase Subunit 2 (IMMP2L))

Reaktivität: Human, Maus

Wirt: Kaninchen

Klonalität: Polyklonal

Konjugat: Dieser IMMP2L Antikörper ist unkonjugiert

Applikation: Western Blotting (WB), ELISA

Produktdetails anti-IMMP2L Antikörper

Bindungsspezifität: AA 30-110

Verwendungszweck: Rabbit Anti-IMP2L Polyclonal Antibody

Spezifität: The antibody detects endogenous levels of IMP2L protein

Aufreinigung: The antibody was affinity-purified from rabbit antiserum by affinity-chromatography using epitope-specific immunogen.

Immunogen: Synthesized peptide derived from part region of human IMP2L protein at AA range: 30-110

Isotyp: IgG

Anwendungsinformationen

Applikationshinweise: Optimal working dilutions should be determined experimentally by the investigator. Suggested starting dilutions are as follows: WB 1:500-2000,ELISA 1:5000-20000

Beschränkungen: Nur für Forschungszwecke einsetzbar

Handhabung

Format: Liquid

Konzentration: 1 mg/mL

Buffer: PBS, 50 % glycerol, 0.05 % Proclin 300, 0.05 %BSA

Konservierungsmittel: ProClin

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

Lagerung: -20 °C

Informationen zur Lagerung: Stable for one year at -20°C from date of shipment. For maximum recovery of product, centrifuge the original vial after thawing and prior to removing the cap. Aliquot to avoid repeated freezing and thawing.

Haltbarkeit: 12 months

Details zu IMMP2L

Target: IMMP2L (Inner Mitochondrial Membrane Peptidase Subunit 2 (IMMP2L))

Andere Bezeichnung: IMP2L

Hintergrund: Mitochondrial inner membrane protease subunit 2, IMP2-like proteinIMMP2L (Inner Mitochondrial Membrane Peptidase Subunit 2) is a Protein Coding gene. Diseases associated with IMMP2L include Deafness, Autosomal Dominant 2A and Gilles De La Tourette Syndrome. Among its related pathways are Protein export. IMMP2L encodes a protein involved in processing the signal peptide sequences used to direct mitochondrial proteins to the mitochondria. The encoded protein resides in the mitochondria and is one of the necessary proteins for the catalytic activity of the mitochondrial inner membrane peptidase (IMP) complex. Two variants that encode the same protein have been described for IMMP2L.

Molekulargewicht: 19kD

Gen-ID: 83943

UniProt: Q96T52