Solute carrier family 2, facilitated glucose transporter member 9; Glucose transporter like protein 9; Glucose transporter type 9; GLUT 9; GLUT-9; GLUT9; GLUTX; GTR9_HUMAN; Human glucose transporter like protein 9; SLC2A9; Solute carrier family 2 (facilitated glucose transporter) member 9; Solute carrier family 2 facilitated glucose transporter member 9; Solute carrier family 2 member 9; Solute carrier family 2 member 9 protein; Solute carrier family 2, facilitated glucose transporter member 9; UAQTL2; Urate voltage driven efflux transporter 1; URATv1 antibody; solute carrier family 2 (facilitated glucose transporter), member 9

For Research Use Only. Not for use in diagnostic procedures.

Polyclonal

Immunogen Affinity Purified

Lyophilized. Each vial contains 5mg BSA, 0.9mg NaCl, 0.2mg Na2HPO4, 0.05mg NaN3.

At -20 degree C for one year. After reconstitution, at 4 degree C for one month. It can also be aliquoted and stored frozen at -20 degree C for a longer time. Avoid repeated freezing and thawing.

Manufactured in an ISO 13485:2003 and EN ISO 13485:2012 Certified Laboratory.

Small volumes of anti-GLUT9 antibody vial(s) may occasionally become entrapped in the seal of the product vial during shipment and storage. If necessary, briefly centrifuge the vial on a tabletop centrifuge to dislodge any liquid in the container`s cap. Certain products may require to ship with dry ice and additional dry ice fee may apply.

Description: Rabbit IgG polyclonal antibody for Solute carrier family 2, facilitated glucose transporter member 9(SLC2A9) detection. Tested with WB in Human.

Background: Solute carrier family 2, facilitated glucose transporter member 9, also known as SLC2A9, is a protein that in humans is encoded by the SLC2A9 gene. This gene encodes a member of the SLC2A facilitative glucose transporter family. Members of this family play a significant role in maintaining glucose homeostasis. This gene is mapped to 4p16.1. The encoded protein may play a role in the development and survival of chondrocytes in cartilage matrices. This gene transports urate and fructose. It may have a role in the urate reabsorption by proximal tubules. This gene also transports glucose at low rate.

Western Blot (WB)

Western Blot Concentration: 0.1-0.5ug/ml

Western blot analysis of GLUT9 expression in HepG2 whole cell lysates (lane 1) and A549 whole cell lysates (lane 2). GLUT9 at 55KD was detected using rabbit anti- GLUT9 Antigen Affinity purified polyclonal antibody at0.5 ug/mL. The blot was developed using chemiluminescence (ECL) method.

55,721 Da

solute carrier family 2 member 9

solute carrier family 2, facilitated glucose transporter member 9

Solute carrier family 2, facilitated glucose transporter member 9

GLUT9; GLUT-9??[Similar Products]

GTR9_HUMAN

This gene encodes a member of the SLC2A facilitative glucose transporter family. Members of this family play a significant role in maintaining glucose homeostasis. The encoded protein may play a role in the development and survival of chondrocytes in cartilage matrices. Two transcript variants encoding distinct isoforms have been identified for this gene. [provided by RefSeq, Jul 2008]

GLUT9: an integral membrane facilitative glucose transporter. One of 13 members of the human equilibrative glucose transport protein family.

Protein type: Transporter; Membrane protein, multi-pass; Membrane protein, integral; Transporter, SLC family

Chromosomal Location of Human Ortholog: 4p16.1

Cellular Component: apical plasma membrane; basolateral plasma membrane; integral to membrane; plasma membrane

Molecular Function: glucose transmembrane transporter activity; sugar:hydrogen ion symporter activity; transmembrane transporter activity; urate transmembrane transporter activity

Biological Process: glucose transport; proton transport; urate metabolic process

Disease: Hypouricemia, Renal, 2

1. Anzai, N., Ichida, K., Jutabha, P., Kimura, T., Babu, E., Jin, C. J., Srivastava, S., Kitamura, K., Hisatome, I., Endou, H., Sakurai, H. Plasma urate level is directly regulated by a voltage-driven urate efflux transporter URATv1 (SLC2A9) in humans. J. Biol. Chem. 283: 26834-26838, 2008. Note: Erratum: J. Biol. Chem. 283: 32152 only, 2008. 2. Preitner, F., Bonny, O., Laverriere, A., Rotman, S., Firsov, D., Da Costa, A., Metref, S., Thorens, B. Glut9 is a major regulator of urate homeostasis and its genetic inactivation induces hyperuricosuria and urate nephropathy. Proc. Nat. Acad. Sci. 106: 15501-15506, 2009.

All of MyBioSource's Products are for scientific laboratory research purposes and are not for diagnostic, therapeutics, prophylactic or in vivo use. Through your purchase, you expressly represent and warrant to MyBioSource that you will properly test and use any Products purchased from MyBioSource in accordance with industry standards. MyBioSource and its authorized distributors reserve the right to refuse to process any order where we reasonably believe that the intended use will fall outside of our acceptable guidelines.

While every efforts were made to ensure the accuracy of the information provided in this datasheet, MyBioSource will not be liable for any omissions or errors contained herein. MyBioSource reserves the right to make changes to this datasheet at any time without prior notice.

It is the responsibility of the customer to report product performance issues to MyBioSource within 30 days of receipt of the product. Please visit our Terms & Conditions page for more information.