GTPBP3 Antikörper (AA 293-320)

Produktnummer ABIN5536595

Produktdetails anti-GTPBP3 Antikörper

Target: GTPBP3 (GTP Binding Protein 3 (Mitochondrial) (GTPBP3))

Bindungsspezifität: AA 293-320

Reaktivität: Human

Wirt: Kaninchen

Klonalität: Polyklonal

Konjugat: Dieser GTPBP3 Antikörper ist unkonjugiert

Applikation: Western Blotting (WB)

Aufreinigung: This antibody is purified through a protein A column, followed by peptide affinity purification.

Immunogen: This GTPBP3 antibody is generated from rabbits immunized with a KLH conjugated synthetic peptide between 293-320 amino acids from the Central region of human GTPBP3.

Isotyp: Ig Fraction

Anwendungsinformationen

Applikationshinweise: For WB starting dilution is: 1:1000

Beschränkungen: Nur für Forschungszwecke einsetzbar

Handhabung

Format: Liquid

Konzentration: 0.44 mg/mL

Buffer: Supplied in PBS with 0.09 % (W/V) sodium azide.

Konservierungsmittel: Sodium azide

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

Lagerung: 4 °C,-20 °C

Informationen zur Lagerung: Store at 4°C for three months and -20°C, stable for up to one year. As with all antibodies care should be taken to avoid repeated freeze thaw cycles. Antibodies should not be exposed to prolonged high temperatures.

Details zu GTPBP3

Target: GTPBP3 (GTP Binding Protein 3 (Mitochondrial) (GTPBP3))

Andere Bezeichnung: GTPBP3 (GTPBP3 Produkte)

Synonyme: GTPBP3 antikoerper, zgc:112394 antikoerper, 2410009F13Rik antikoerper, AI607903 antikoerper, GTPBG3 antikoerper, MSS1 antikoerper, MTGP1 antikoerper, THDF1 antikoerper, GTP binding protein 3, mitochondrial antikoerper, GTP binding protein 3 antikoerper, GTPBP3 antikoerper, Gtpbp3 antikoerper, gtpbp3 antikoerper

Hintergrund: This locus encodes a GTP-binding protein. The encoded protein is localized to the mitochondria and may play a role in mitochondrial tRNA modification. Polymorphisms at this locus may be associated with severity of aminoglycoside-induced deafness, a disease associated with a mutation in the 12S rRNA. Alternatively spliced transcript variants encoding different isoforms have been described.

Molekulargewicht: 52 kDa

Gen-ID: 84705

UniProt: Q969Y2