Solute Carrier Family 52 (Riboflavin Transporter), Member 3 (SLC52A3) (AA 200-300) antibody

Catalog No. ABIN7270472

Product Details

Target: Solute Carrier Family 52 (Riboflavin Transporter), Member 3 (SLC52A3)

Binding Specificity: AA 200-300

Reactivity: Human

Host: Rabbit

Clonality: Polyclonal

Conjugate: Un-conjugated

Application: Western Blotting (WB)

Purpose: SLC52A3 Rabbit pAb

Sequence: PGMEAPLSHL ESRYLPAHFS PLVFFLLLSI MMACCLVAFF VLQRQPRCWE ASVEDLLNDQ VTLHSIRPRE ENDLGPAGTV DSSQGQGYLE EKAAPCCPAH L

Cross-Reactivity: Mouse

Characteristics: Polyclonal Antibodies

Purification: Affinity purification

Immunogen: A synthetic peptide corresponding to a sequence within amino acids 200-300 of human SLC52A3 (NP_212134.3).

Isotype: IgG

Application Details

Application Notes: WB,1:500 - 1:2000

Restrictions: For Research Use only

Handling

Format: Liquid

Buffer: PBS with 0.02 % sodium azide,50 % glycerol, pH 7.3.

Preservative: Sodium azide

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

Storage: -20 °C

Storage Comment: Store at -20°C. Avoid freeze / thaw cycles.

Target Details

Target: Solute Carrier Family 52 (Riboflavin Transporter), Member 3 (SLC52A3)

Alternative Name: SLC52A3 (SLC52A3 Products)

Synonyms: 2310046K01Rik antibody, RFT2 antibody, RGD1304644 antibody, Rft2 antibody, rRFT2 antibody, C13H20orf54 antibody, C20orf54 antibody, BVVLS antibody, BVVLS1 antibody, RFVT3 antibody, bA371L19.1 antibody, hRFT2 antibody, RFT2-A antibody, rft2a antibody, slc52a3a antibody, zgc:136909 antibody, solute carrier protein family 52, member 3 antibody, solute carrier family 52 member 3 antibody, CT054 protein antibody, solute carrier family 52 (riboflavin transporter), member 3 antibody, Slc52a3 antibody, SLC52A3 antibody, ct054 antibody, slc52a3 antibody

Background: This gene encodes a riboflavin transporter protein that is strongly expressed in the intestine and likely plays a role in intestinal absorption of riboflavin. The protein is predicted to have eleven transmembrane domains and a cell surface localization signal in the C-terminus. Mutations at this locus have been associated with Brown-Vialetto-Van Laere syndrome and Fazio-Londe disease.,SLC52A3,BVVLS,BVVLS1,C20orf54,RFT2,RFVT3,bA371L19.1,hRFT2,Cancer,Signal Transduction,Endocrine & Metabolism,SLC52A3

Molecular Weight: 45kDa/50kDa

Gene ID: 113278

UniProt: Q9NQ40

Pathways: Sensory Perception of Sound