BTAF1 Antikörper (AA 240-320)

Produktnummer ABIN7229726

Dieser Anti-BTAF1 Antikörper ist ein Kaninchen Polyklonal Antikörper zur Detektion von BTAF1 in WB und ELISA. Geeignet für Human, Maus und Ratte.

Kurzübersicht für BTAF1 Antikörper (AA 240-320) (ABIN7229726)

Target: BTAF1 (TBP-Associated Factor 172 (BTAF1))

Reaktivität: Human, Maus, Ratte

Wirt: Kaninchen

Klonalität: Polyklonal

Konjugat: Dieser BTAF1 Antikörper ist unkonjugiert

Applikation: Western Blotting (WB), ELISA

Produktdetails anti-BTAF1 Antikörper

Bindungsspezifität: AA 240-320

Verwendungszweck: MOT1 Polyclonal Antibody

Spezifität: The antibody detects endogenous levels of MOT1 protein

Aufreinigung: The antibody was affinity-purified from rabbit serum by affinity-chromatography using specific immunogen

Immunogen: Synthesized peptide derived from part region of human MOT1 protein at AA range: 240-320

Isotyp: IgG

Anwendungsinformationen

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

Kommentare:

Primary Antibody

Beschränkungen: Nur für Forschungszwecke einsetzbar

Handhabung

Format: Liquid

Konzentration: 1 mg/mL

Buffer: PBS, pH 7.4, containing 0.02 % Sodium Azide as preservative and 50 % Glycerol.

Konservierungsmittel: Sodium azide

Vorsichtsmaßnahmen: This product contains Sodium azide: 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.

Details zu BTAF1

Target: BTAF1 (TBP-Associated Factor 172 (BTAF1))

Andere Bezeichnung: MOT1

Hintergrund: Rabbit Anti-MOT1 Polyclonal Antibody,Monocarboxylate transporter 1, MCT 1, Solute carrier family 16 member 1,SLC16A1 (Solute Carrier Family 16 Member 1) is a Protein Coding gene. Diseases associated with SLC16A1 include Erythrocyte Lactate Transporter Defect and Monocarboxylate Transporter 1 Deficiency. Among its related pathways are Cell surface interactions at the vascular wall and Metabolism. The protein encoded by SLC16A1 is a proton-linked monocarboxylate transporter that catalyzes the movement of many monocarboxylates, such as lactate and pyruvate, across the plasma membrane. Mutations in SLC16A1 are associated with erythrocyte lactate transporter defect. Alternatively spliced transcript variants have been found for SLC16A1.,MOT1

Molekulargewicht: observerd band 55kDa

Gen-ID: 6566

UniProt: P53985