BTAF1 antibody (AA 240-320)

Catalog No. ABIN7229726

The Rabbit Polyclonal anti-BTAF1 antibody (ABIN7229726) specifically detects BTAF1 in WB and ELISA. The antibody is reactive with Human, Mouse and Rat samples.

Quick Overview for BTAF1 antibody (AA 240-320) (ABIN7229726)

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

Reactivity: Human, Mouse, Rat

Host: Rabbit

Clonality: Polyclonal

Conjugate: This BTAF1 antibody is un-conjugated

Application: Western Blotting (WB), ELISA

Product Details anti-BTAF1 Antibody

Binding Specificity: AA 240-320

Purpose: Rabbit Anti-MOT1 Polyclonal Antibody

Specificity: The antibody detects endogenous levels of MOT1 protein

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

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

Isotype: IgG

Application Details

Application Notes: 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

Handling

Format: Liquid

Concentration: 1 mg/mL

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

Preservative: ProClin

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

Storage: -20 °C

Storage Comment: 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.

Expiry Date: 12 months

Target Details for BTAF1

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

Alternative Name: MOT1

Background: 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.

Molecular Weight: 55kD

Gene ID: 6566

UniProt: P53985