SLC52A3 Antibody

Product Specifications

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.

NCBI Gene ID

113278

Swiss Prot

Q9NQ40

Host

Rabbit

Reactivity

Mouse

Immunogen

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

Clonality

Polyclonal

Conjugation

Unconjugated

Type

Primary Antibodies

Field of Research

Cancer, Signal Transduction

Purification

Affinity purification

Positive Control

Mouse kidney

Concentration

Batch dependent

Buffer

PBS with 0.02% sodium azide, 50% glycerol, pH7.3.

Modification

None

Shipping Conditions

Blue Ice

Storage Conditions

Store at -20˚ C. Avoid freeze / thaw cycles.

Calculated Molecular Weight

Observed: 51kDa

Fragment

IgG

Applications Notes

WB: 1:500 - 1:2000

Symbol

SLC52A3

NCBI Official Name

Solute carrier family 52 member 3

NCBI Organism

Homo sapiens

Other Product Names

BVVLS, BVVLS1, C20orf54, RFT2, RFVT3, bA371L19.1, hRFT2, solute carrier family 52, riboflavin transporter, member 3, SLC52A3a, SLC52A3b, riboflavin transporter 2, solute carrier family 52 (riboflavin transporter), member 3