BTAF1 anticorps (AA 240-320)

N° du produit ABIN7229726

Cet anticorps anti-BTAF1 Polyclonal Lapin (ABIN7229726) détecte spécifiquement BTAF1 dans WB et ELISA. L’anticorps est réactif avec des échantillons de Humain, Souris et Rat.

Aperçu rapide pour BTAF1 anticorps (AA 240-320) (ABIN7229726)

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

Reactivité: Humain, Souris, Rat

Hôte: Lapin

Clonalité: Polyclonal

Conjugué: Cet anticorp BTAF1 est non-conjugé

Application: Western Blotting (WB), ELISA

Détail du produit anti-BTAF1 anticorps

Épitope: AA 240-320

Fonction: Rabbit Anti-MOT1 Polyclonal Antibody

Specificité: The antibody detects endogenous levels of MOT1 protein

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

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

Isotype: IgG

Information d'application

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

Restrictions: For Research Use only

Stockage

Format: Liquid

Concentration: 1 mg/mL

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

Agent conservateur: ProClin

Précaution d'utilisation: This product contains ProClin: a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.

Stock: -20 °C

Stockage commentaire: 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.

Date de péremption: 12 months

Détails sur BTAF1

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

Autre désignation: MOT1

Sujet: Monocarboxylate transporter 1, MCT 1, Solute carrier family 16 member 1SLC16A1 (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.

Poids moléculaire: 55kD

ID gène: 6566

UniProt: P53985