SLC52A3 Antilichaam

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.

113278

Q9NQ40

Mouse

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

Unconjugated

Primary Antibodies

Cancer, Signal Transduction

Affinity purification

Mouse kidney

Batch dependent

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

None

Blue Ice

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

Observed: 51kDa

IgG

WB: 1:500 - 1:2000

SLC52A3

Solute carrier family 52 member 3

Homo sapiens

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

WB

Liquid