SLC19A2 antibody

Catalog No. ABIN7468999

The Rabbit Polyclonal anti-SLC19A2 antibody has been validated for WB, ICC and IF. It is suitable to detect SLC19A2 in samples from Human.

Quick Overview for SLC19A2 antibody (ABIN7468999)

Target: SLC19A2 (Solute Carrier Family 19 (Thiamine Transporter), Member 2 (SLC19A2))

Reactivity: Human

Host: Rabbit

Clonality: Polyclonal

Conjugate: This SLC19A2 antibody is un-conjugated

Application: Western Blotting (WB), Immunocytochemistry (ICC), Immunofluorescence (IF)

Product Details anti-SLC19A2 Antibody

Cross-Reactivity: Human, Mouse, Rat

Purification: Purified by antigen-affinity chromatography.

Immunogen: Recombinant protein encompassing a sequence within the center region of human SLC19A2. The exact sequence is proprietary.

Isotype: IgG

Application Details

Application Notes: WB: 1:500-1:3000. ICC/IF: 1:100-1:1000. Optimal dilutions/concentrations should be determined by the researcher. Not tested in other applications.

Comment:

Positive Control: mouse liver

Restrictions: For Research Use only

Handling

Format: Liquid

Concentration: 1.3 mg/mL

Buffer: 1XPBS ( pH 7), 20 % Glycerol, 0.025 % ProClin 300

Preservative: ProClin

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

Storage: 4 °C,-20 °C

Storage Comment: Store as concentrated solution. Centrifuge briefly prior to opening vial. For short-term storage (1-2 weeks), store at 4°C. For long-term storage, aliquot and store at -20°C or below. Avoid multiple freeze-thaw cycles.

Target Details for SLC19A2

Target: SLC19A2 (Solute Carrier Family 19 (Thiamine Transporter), Member 2 (SLC19A2))

Alternative Name: solute carrier family 19 member 2

Background:

Synonyms: solute carrier family 19 member 2 , TC1 , THMD1 , THT1 , THTR1 , TRMA

Background: This gene encodes the thiamin transporter protein. Mutations in this gene cause thiamin-responsive megaloblastic anemia syndrome (TRMA), which is an autosomal recessive disorder characterized by diabetes mellitus, megaloblastic anemia and sensorineural deafness. [provided by RefSeq]

Molecular Weight: 55 kDa

Gene ID: 10560

UniProt: O60779

Pathways: Dicarboxylic Acid Transport