SLC19A2 antibody (AA 21-120) (Alexa Fluor 680)

Catalog No. ABIN6980683

Product Details anti-SLC19A2 Antibody (Alexa Fluor 680)

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

Binding Specificity: AA 21-120

Reactivity: Mouse

Host: Rabbit

Clonality: Polyclonal

Conjugate: This SLC19A2 antibody is conjugated to Alexa Fluor 680

Application: Western Blotting (WB), Immunofluorescence (Cultured Cells) (IF (cc)), Immunofluorescence (Paraffin-embedded Sections) (IF (p))

Specificity: Possible cross-reactivity with SLC19A3 in human samples

Cross-Reactivity: Mouse

Predicted Reactivity: Human,Rat,Dog,Cow,Pig,Horse,Rabbit

Purification: Purified by Protein A.

Immunogen: KLH conjugated synthetic peptide derived from human SLC19A2

Isotype: IgG

Application Details

Application Notes: IF(IHC-P) 1:50-200
IF(IHC-F) 1:50-200
IF(ICC) 1:50-200

Restrictions: For Research Use only

Handling

Format: Liquid

Concentration: 1 μg/μL

Buffer: Aqueous buffered solution containing 0.01M TBS ( pH 7.4) with 1 % BSA, 0.03 % Proclin300 and 50 % Glycerol.

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: Store at -20°C. Aliquot into multiple vials to avoid repeated freeze-thaw cycles.

Expiry Date: 12 months

Target Details for SLC19A2

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

Alternative Name: SLC19A2 (SLC19A2 Products)

Synonyms: SLC19A2 antibody, TC1 antibody, THMD1 antibody, THT1 antibody, THTR1 antibody, TRMA antibody, solute carrier family 19 member 2 antibody, solute carrier family 19 (thiamine transporter), member 2 antibody, Slc19a2 antibody, SLC19A2 antibody, slc19a2 antibody

Background:

Synonyms: Thiamine transporter 1, S19A2_HUMAN, SLC19A2, Solute carrier family 19 member 2, TC1, Thiamine carrier 1, THT1, ThTr 1, ThTr-1, 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, Jul 2008]

Gene ID: 10560

UniProt: O60779

Pathways: Dicarboxylic Acid Transport