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Sodium/glucose cotransporter 1 (Na( )/glucose cotransporter 1) (High affinity sodium-glucose cotransporter) (Solute carrier family 5 member 1)

 SC5A1_HUMAN             Reviewed;         664 AA.
P13866; B2R7E2; B7Z4Q9; B7ZA69;
01-JAN-1990, integrated into UniProtKB/Swiss-Prot.
01-JAN-1990, sequence version 1.
22-NOV-2017, entry version 181.
RecName: Full=Sodium/glucose cotransporter 1;
Short=Na(+)/glucose cotransporter 1;
AltName: Full=High affinity sodium-glucose cotransporter;
AltName: Full=Solute carrier family 5 member 1;
Name=SLC5A1; Synonyms=NAGT, SGLT1;
Homo sapiens (Human).
Eukaryota; Metazoa; Chordata; Craniata; Vertebrata; Euteleostomi;
Mammalia; Eutheria; Euarchontoglires; Primates; Haplorrhini;
Catarrhini; Hominidae; Homo.
NCBI_TaxID=9606;
[1]
NUCLEOTIDE SEQUENCE [MRNA] (ISOFORM 1).
PubMed=2490366; DOI=10.1073/pnas.86.15.5748;
Hediger M.A., Turk E., Wright E.M.;
"Homology of the human intestinal Na+/glucose and Escherichia coli
Na+/proline cotransporters.";
Proc. Natl. Acad. Sci. U.S.A. 86:5748-5752(1989).
[2]
NUCLEOTIDE SEQUENCE [GENOMIC DNA], AND VARIANT GGM GLY-28.
PubMed=8195156;
Turk E., Martin M.G., Wright E.M.;
"Structure of the human Na+/glucose cotransporter gene SGLT1.";
J. Biol. Chem. 269:15204-15209(1994).
[3]
NUCLEOTIDE SEQUENCE [LARGE SCALE MRNA] (ISOFORM 1).
PubMed=15461802; DOI=10.1186/gb-2004-5-10-r84;
Collins J.E., Wright C.L., Edwards C.A., Davis M.P., Grinham J.A.,
Cole C.G., Goward M.E., Aguado B., Mallya M., Mokrab Y., Huckle E.J.,
Beare D.M., Dunham I.;
"A genome annotation-driven approach to cloning the human ORFeome.";
Genome Biol. 5:R84.1-R84.11(2004).
[4]
NUCLEOTIDE SEQUENCE [LARGE SCALE MRNA] (ISOFORMS 1 AND 2).
TISSUE=Heart, and Trachea;
PubMed=14702039; DOI=10.1038/ng1285;
Ota T., Suzuki Y., Nishikawa T., Otsuki T., Sugiyama T., Irie R.,
Wakamatsu A., Hayashi K., Sato H., Nagai K., Kimura K., Makita H.,
Sekine M., Obayashi M., Nishi T., Shibahara T., Tanaka T., Ishii S.,
Yamamoto J., Saito K., Kawai Y., Isono Y., Nakamura Y., Nagahari K.,
Murakami K., Yasuda T., Iwayanagi T., Wagatsuma M., Shiratori A.,
Sudo H., Hosoiri T., Kaku Y., Kodaira H., Kondo H., Sugawara M.,
Takahashi M., Kanda K., Yokoi T., Furuya T., Kikkawa E., Omura Y.,
Abe K., Kamihara K., Katsuta N., Sato K., Tanikawa M., Yamazaki M.,
Ninomiya K., Ishibashi T., Yamashita H., Murakawa K., Fujimori K.,
Tanai H., Kimata M., Watanabe M., Hiraoka S., Chiba Y., Ishida S.,
Ono Y., Takiguchi S., Watanabe S., Yosida M., Hotuta T., Kusano J.,
Kanehori K., Takahashi-Fujii A., Hara H., Tanase T.-O., Nomura Y.,
Togiya S., Komai F., Hara R., Takeuchi K., Arita M., Imose N.,
Musashino K., Yuuki H., Oshima A., Sasaki N., Aotsuka S.,
Yoshikawa Y., Matsunawa H., Ichihara T., Shiohata N., Sano S.,
Moriya S., Momiyama H., Satoh N., Takami S., Terashima Y., Suzuki O.,
Nakagawa S., Senoh A., Mizoguchi H., Goto Y., Shimizu F., Wakebe H.,
Hishigaki H., Watanabe T., Sugiyama A., Takemoto M., Kawakami B.,
Yamazaki M., Watanabe K., Kumagai A., Itakura S., Fukuzumi Y.,
Fujimori Y., Komiyama M., Tashiro H., Tanigami A., Fujiwara T.,
Ono T., Yamada K., Fujii Y., Ozaki K., Hirao M., Ohmori Y.,
Kawabata A., Hikiji T., Kobatake N., Inagaki H., Ikema Y., Okamoto S.,
Okitani R., Kawakami T., Noguchi S., Itoh T., Shigeta K., Senba T.,
Matsumura K., Nakajima Y., Mizuno T., Morinaga M., Sasaki M.,
Togashi T., Oyama M., Hata H., Watanabe M., Komatsu T.,
Mizushima-Sugano J., Satoh T., Shirai Y., Takahashi Y., Nakagawa K.,
Okumura K., Nagase T., Nomura N., Kikuchi H., Masuho Y., Yamashita R.,
Nakai K., Yada T., Nakamura Y., Ohara O., Isogai T., Sugano S.;
"Complete sequencing and characterization of 21,243 full-length human
cDNAs.";
Nat. Genet. 36:40-45(2004).
[5]
NUCLEOTIDE SEQUENCE [LARGE SCALE GENOMIC DNA].
PubMed=10591208; DOI=10.1038/990031;
Dunham I., Hunt A.R., Collins J.E., Bruskiewich R., Beare D.M.,
Clamp M., Smink L.J., Ainscough R., Almeida J.P., Babbage A.K.,
Bagguley C., Bailey J., Barlow K.F., Bates K.N., Beasley O.P.,
Bird C.P., Blakey S.E., Bridgeman A.M., Buck D., Burgess J.,
Burrill W.D., Burton J., Carder C., Carter N.P., Chen Y., Clark G.,
Clegg S.M., Cobley V.E., Cole C.G., Collier R.E., Connor R.,
Conroy D., Corby N.R., Coville G.J., Cox A.V., Davis J., Dawson E.,
Dhami P.D., Dockree C., Dodsworth S.J., Durbin R.M., Ellington A.G.,
Evans K.L., Fey J.M., Fleming K., French L., Garner A.A.,
Gilbert J.G.R., Goward M.E., Grafham D.V., Griffiths M.N.D., Hall C.,
Hall R.E., Hall-Tamlyn G., Heathcott R.W., Ho S., Holmes S.,
Hunt S.E., Jones M.C., Kershaw J., Kimberley A.M., King A.,
Laird G.K., Langford C.F., Leversha M.A., Lloyd C., Lloyd D.M.,
Martyn I.D., Mashreghi-Mohammadi M., Matthews L.H., Mccann O.T.,
Mcclay J., Mclaren S., McMurray A.A., Milne S.A., Mortimore B.J.,
Odell C.N., Pavitt R., Pearce A.V., Pearson D., Phillimore B.J.C.T.,
Phillips S.H., Plumb R.W., Ramsay H., Ramsey Y., Rogers L., Ross M.T.,
Scott C.E., Sehra H.K., Skuce C.D., Smalley S., Smith M.L.,
Soderlund C., Spragon L., Steward C.A., Sulston J.E., Swann R.M.,
Vaudin M., Wall M., Wallis J.M., Whiteley M.N., Willey D.L.,
Williams L., Williams S.A., Williamson H., Wilmer T.E., Wilming L.,
Wright C.L., Hubbard T., Bentley D.R., Beck S., Rogers J., Shimizu N.,
Minoshima S., Kawasaki K., Sasaki T., Asakawa S., Kudoh J.,
Shintani A., Shibuya K., Yoshizaki Y., Aoki N., Mitsuyama S.,
Roe B.A., Chen F., Chu L., Crabtree J., Deschamps S., Do A., Do T.,
Dorman A., Fang F., Fu Y., Hu P., Hua A., Kenton S., Lai H., Lao H.I.,
Lewis J., Lewis S., Lin S.-P., Loh P., Malaj E., Nguyen T., Pan H.,
Phan S., Qi S., Qian Y., Ray L., Ren Q., Shaull S., Sloan D., Song L.,
Wang Q., Wang Y., Wang Z., White J., Willingham D., Wu H., Yao Z.,
Zhan M., Zhang G., Chissoe S., Murray J., Miller N., Minx P.,
Fulton R., Johnson D., Bemis G., Bentley D., Bradshaw H., Bourne S.,
Cordes M., Du Z., Fulton L., Goela D., Graves T., Hawkins J.,
Hinds K., Kemp K., Latreille P., Layman D., Ozersky P., Rohlfing T.,
Scheet P., Walker C., Wamsley A., Wohldmann P., Pepin K., Nelson J.,
Korf I., Bedell J.A., Hillier L.W., Mardis E., Waterston R.,
Wilson R., Emanuel B.S., Shaikh T., Kurahashi H., Saitta S.,
Budarf M.L., McDermid H.E., Johnson A., Wong A.C.C., Morrow B.E.,
Edelmann L., Kim U.J., Shizuya H., Simon M.I., Dumanski J.P.,
Peyrard M., Kedra D., Seroussi E., Fransson I., Tapia I., Bruder C.E.,
O'Brien K.P., Wilkinson P., Bodenteich A., Hartman K., Hu X.,
Khan A.S., Lane L., Tilahun Y., Wright H.;
"The DNA sequence of human chromosome 22.";
Nature 402:489-495(1999).
[6]
NUCLEOTIDE SEQUENCE [LARGE SCALE GENOMIC DNA].
Mural R.J., Istrail S., Sutton G.G., Florea L., Halpern A.L.,
Mobarry C.M., Lippert R., Walenz B., Shatkay H., Dew I., Miller J.R.,
Flanigan M.J., Edwards N.J., Bolanos R., Fasulo D., Halldorsson B.V.,
Hannenhalli S., Turner R., Yooseph S., Lu F., Nusskern D.R.,
Shue B.C., Zheng X.H., Zhong F., Delcher A.L., Huson D.H.,
Kravitz S.A., Mouchard L., Reinert K., Remington K.A., Clark A.G.,
Waterman M.S., Eichler E.E., Adams M.D., Hunkapiller M.W., Myers E.W.,
Venter J.C.;
Submitted (JUL-2005) to the EMBL/GenBank/DDBJ databases.
[7]
TOPOLOGY, MUTAGENESIS OF ASN-248, AND GLYCOSYLATION AT ASN-248.
PubMed=8567640; DOI=10.1074/jbc.271.4.1925;
Turk E., Kerner C.J., Lostao M.P., Wright E.M.;
"Membrane topology of the human Na+/glucose cotransporter SGLT1.";
J. Biol. Chem. 271:1925-1934(1996).
[8]
VARIANT GGM ASN-28.
PubMed=2008213; DOI=10.1038/350354a0;
Turk E., Zabel B., Mundlos S., Dyer J., Wright E.M.;
"Glucose/galactose malabsorption caused by a defect in the Na+/glucose
cotransporter.";
Nature 350:354-356(1991).
[9]
VARIANTS GGM ARG-318 AND VAL-468.
PubMed=10036327; DOI=10.1016/S0925-4439(98)00109-4;
Lam J.T., Martin M.G., Turk E., Hirayama B.A., Bosshard N.U.,
Steinmann B., Wright E.M.;
"Missense mutations in SGLT1 cause glucose-galactose malabsorption by
trafficking defects.";
Biochim. Biophys. Acta 1453:297-303(1999).
[10]
VARIANT GGM TRP-135.
PubMed=11406349; DOI=10.1016/S0925-4439(01)00043-6;
Kasahara M., Maeda M., Hayashi S., Mori Y., Abe T.;
"A missense mutation in the Na(+)/glucose cotransporter gene SGLT1 in
a patient with congenital glucose-galactose malabsorption: normal
trafficking but inactivation of the mutant protein.";
Biochim. Biophys. Acta 1536:141-147(2001).
-!- FUNCTION: Actively transports glucose into cells by Na(+)
cotransport with a Na(+) to glucose coupling ratio of 2:1.
Efficient substrate transport in mammalian kidney is provided by
the concerted action of a low affinity high capacity and a high
affinity low capacity Na(+)/glucose cotransporter arranged in
series along kidney proximal tubules.
-!- INTERACTION:
P00533:EGFR; NbExp=3; IntAct=EBI-1772443, EBI-297353;
-!- SUBCELLULAR LOCATION: Membrane; Multi-pass membrane protein.
-!- ALTERNATIVE PRODUCTS:
Event=Alternative splicing; Named isoforms=2;
Name=1;
IsoId=P13866-1; Sequence=Displayed;
Name=2;
IsoId=P13866-2; Sequence=VSP_044782;
Note=No experimental confirmation available.;
-!- TISSUE SPECIFICITY: Expressed mainly in intestine and kidney.
-!- PTM: N-glycosylation is not necessary for the cotransporter
function. {ECO:0000269|PubMed:8567640}.
-!- DISEASE: Congenital glucose/galactose malabsorption (GGM)
[MIM:606824]: Intestinal monosaccharide transporter deficiency. It
is an autosomal recessive disorder manifesting itself within the
first weeks of life. It is characterized by severe diarrhea and
dehydration which are usually fatal unless glucose and galactose
are eliminated from the diet. {ECO:0000269|PubMed:10036327,
ECO:0000269|PubMed:11406349, ECO:0000269|PubMed:2008213,
ECO:0000269|PubMed:8195156}. Note=The disease is caused by
mutations affecting the gene represented in this entry.
-!- SIMILARITY: Belongs to the sodium:solute symporter (SSF) (TC
2.A.21) family. {ECO:0000305}.
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EMBL; M24847; AAA60320.1; -; mRNA.
EMBL; L29339; AAB59448.1; -; Genomic_DNA.
EMBL; L29328; AAB59448.1; JOINED; Genomic_DNA.
EMBL; L29330; AAB59448.1; JOINED; Genomic_DNA.
EMBL; L29329; AAB59448.1; JOINED; Genomic_DNA.
EMBL; L29331; AAB59448.1; JOINED; Genomic_DNA.
EMBL; L29332; AAB59448.1; JOINED; Genomic_DNA.
EMBL; L29333; AAB59448.1; JOINED; Genomic_DNA.
EMBL; L29334; AAB59448.1; JOINED; Genomic_DNA.
EMBL; L29335; AAB59448.1; JOINED; Genomic_DNA.
EMBL; L29336; AAB59448.1; JOINED; Genomic_DNA.
EMBL; L29337; AAB59448.1; JOINED; Genomic_DNA.
EMBL; L29338; AAB59448.1; JOINED; Genomic_DNA.
EMBL; CR456579; CAG30465.1; -; mRNA.
EMBL; AK297665; BAH12645.1; -; mRNA.
EMBL; AK312948; BAG35789.1; -; mRNA.
EMBL; AK316184; BAH14555.1; -; mRNA.
EMBL; AL022321; -; NOT_ANNOTATED_CDS; Genomic_DNA.
EMBL; Z74021; -; NOT_ANNOTATED_CDS; Genomic_DNA.
EMBL; Z80998; -; NOT_ANNOTATED_CDS; Genomic_DNA.
EMBL; Z83839; -; NOT_ANNOTATED_CDS; Genomic_DNA.
EMBL; Z83849; -; NOT_ANNOTATED_CDS; Genomic_DNA.
EMBL; CH471095; EAW60006.1; -; Genomic_DNA.
CCDS; CCDS13902.1; -. [P13866-1]
CCDS; CCDS58805.1; -. [P13866-2]
PIR; A33545; A33545.
RefSeq; NP_000334.1; NM_000343.3. [P13866-1]
RefSeq; NP_001243243.1; NM_001256314.1. [P13866-2]
UniGene; Hs.1964; -.
ProteinModelPortal; P13866; -.
BioGrid; 112414; 2.
IntAct; P13866; 1.
STRING; 9606.ENSP00000266088; -.
BindingDB; P13866; -.
ChEMBL; CHEMBL4979; -.
DrugBank; DB08907; Canagliflozin.
GuidetoPHARMACOLOGY; 915; -.
TCDB; 2.A.21.3.1; the solute:sodium symporter (sss) family.
iPTMnet; P13866; -.
PhosphoSitePlus; P13866; -.
BioMuta; SLC5A1; -.
DMDM; 127803; -.
EPD; P13866; -.
MaxQB; P13866; -.
PaxDb; P13866; -.
PeptideAtlas; P13866; -.
PRIDE; P13866; -.
DNASU; 6523; -.
Ensembl; ENST00000266088; ENSP00000266088; ENSG00000100170. [P13866-1]
Ensembl; ENST00000543737; ENSP00000444898; ENSG00000100170. [P13866-2]
GeneID; 6523; -.
KEGG; hsa:6523; -.
UCSC; uc003amc.4; human. [P13866-1]
CTD; 6523; -.
DisGeNET; 6523; -.
EuPathDB; HostDB:ENSG00000100170.9; -.
GeneCards; SLC5A1; -.
HGNC; HGNC:11036; SLC5A1.
HPA; CAB015467; -.
HPA; HPA051805; -.
HPA; HPA055106; -.
MalaCards; SLC5A1; -.
MIM; 182380; gene.
MIM; 606824; phenotype.
neXtProt; NX_P13866; -.
OpenTargets; ENSG00000100170; -.
Orphanet; 35710; Glucose-galactose malabsorption.
PharmGKB; PA308; -.
eggNOG; ENOG410IP49; Eukaryota.
eggNOG; COG4146; LUCA.
GeneTree; ENSGT00760000118955; -.
HOVERGEN; HBG052859; -.
InParanoid; P13866; -.
KO; K14158; -.
OMA; CWTDLIQ; -.
OrthoDB; EOG091G077U; -.
PhylomeDB; P13866; -.
TreeFam; TF352855; -.
Reactome; R-HSA-189200; Cellular hexose transport.
Reactome; R-HSA-5656364; Defective SLC5A1 causes congenital glucose/galactose malabsorption (GGM).
Reactome; R-HSA-8981373; Intestinal hexose absorption.
ChiTaRS; SLC5A1; human.
GeneWiki; SLC5A1; -.
GenomeRNAi; 6523; -.
PRO; PR:P13866; -.
Proteomes; UP000005640; Chromosome 22.
Bgee; ENSG00000100170; -.
CleanEx; HS_SLC5A1; -.
Genevisible; P13866; HS.
GO; GO:0016324; C:apical plasma membrane; IEA:Ensembl.
GO; GO:0031526; C:brush border membrane; IEA:Ensembl.
GO; GO:0005911; C:cell-cell junction; IEA:Ensembl.
GO; GO:0070062; C:extracellular exosome; IDA:UniProtKB.
GO; GO:0005887; C:integral component of plasma membrane; TAS:ProtInc.
GO; GO:0005886; C:plasma membrane; TAS:Reactome.
GO; GO:0005412; F:glucose:sodium symporter activity; IDA:MGI.
GO; GO:0015758; P:glucose transport; IMP:MGI.
GO; GO:0001951; P:intestinal D-glucose absorption; IBA:GO_Central.
GO; GO:0106001; P:intestinal hexose absorption; TAS:Reactome.
InterPro; IPR001734; Na/solute_symporter.
InterPro; IPR018212; Na/solute_symporter_CS.
Pfam; PF00474; SSF; 1.
TIGRFAMs; TIGR00813; sss; 1.
PROSITE; PS00456; NA_SOLUT_SYMP_1; 1.
PROSITE; PS00457; NA_SOLUT_SYMP_2; 1.
PROSITE; PS50283; NA_SOLUT_SYMP_3; 1.
1: Evidence at protein level;
Alternative splicing; Complete proteome; Disease mutation;
Disulfide bond; Glycoprotein; Ion transport; Membrane; Phosphoprotein;
Polymorphism; Reference proteome; Sodium; Sodium transport;
Sugar transport; Symport; Transmembrane; Transmembrane helix;
Transport.
CHAIN 1 664 Sodium/glucose cotransporter 1.
/FTId=PRO_0000105366.
TOPO_DOM 1 28 Extracellular. {ECO:0000255}.
TRANSMEM 29 49 Helical. {ECO:0000255}.
TOPO_DOM 50 64 Cytoplasmic. {ECO:0000255}.
TRANSMEM 65 85 Helical. {ECO:0000255}.
TOPO_DOM 86 105 Extracellular. {ECO:0000255}.
TRANSMEM 106 126 Helical. {ECO:0000255}.
TOPO_DOM 127 142 Cytoplasmic. {ECO:0000255}.
TRANSMEM 143 163 Helical. {ECO:0000255}.
TOPO_DOM 164 178 Extracellular. {ECO:0000255}.
TRANSMEM 179 201 Helical. {ECO:0000255}.
TOPO_DOM 202 208 Cytoplasmic. {ECO:0000255}.
TRANSMEM 209 229 Helical. {ECO:0000255}.
TOPO_DOM 230 277 Extracellular. {ECO:0000255}.
TRANSMEM 278 298 Helical. {ECO:0000255}.
TOPO_DOM 299 313 Cytoplasmic. {ECO:0000255}.
TRANSMEM 314 334 Helical. {ECO:0000255}.
TOPO_DOM 335 380 Extracellular. {ECO:0000255}.
TRANSMEM 381 401 Helical. {ECO:0000255}.
TOPO_DOM 402 423 Cytoplasmic. {ECO:0000255}.
TRANSMEM 424 444 Helical. {ECO:0000255}.
TOPO_DOM 445 455 Extracellular. {ECO:0000255}.
TRANSMEM 456 476 Helical. {ECO:0000255}.
TOPO_DOM 477 484 Cytoplasmic. {ECO:0000255}.
TRANSMEM 485 505 Helical. {ECO:0000255}.
TOPO_DOM 506 526 Extracellular. {ECO:0000255}.
INTRAMEM 527 563 Helical. {ECO:0000255}.
TOPO_DOM 564 643 Extracellular. {ECO:0000255}.
TRANSMEM 644 664 Helical. {ECO:0000255}.
BINDING 457 457 Glucose. {ECO:0000250}.
SITE 43 43 Implicated in sodium coupling.
{ECO:0000250}.
SITE 300 300 Implicated in sodium coupling.
{ECO:0000250}.
SITE 460 460 Involved in sugar-binding/transport and
inhibitor binding. {ECO:0000250}.
MOD_RES 587 587 Phosphothreonine.
{ECO:0000250|UniProtKB:Q8C3K6}.
CARBOHYD 248 248 N-linked (GlcNAc...) asparagine.
{ECO:0000269|PubMed:8567640}.
DISULFID 255 610 {ECO:0000250}.
VAR_SEQ 1 127 Missing (in isoform 2).
{ECO:0000303|PubMed:14702039}.
/FTId=VSP_044782.
VARIANT 28 28 D -> G (in GGM; dbSNP:rs121912669).
{ECO:0000269|PubMed:8195156}.
/FTId=VAR_013630.
VARIANT 28 28 D -> N (in GGM; dbSNP:rs121912668).
{ECO:0000269|PubMed:2008213}.
/FTId=VAR_007168.
VARIANT 51 51 N -> S (in dbSNP:rs17683011).
/FTId=VAR_029147.
VARIANT 135 135 R -> W (in GGM; loss of activity).
{ECO:0000269|PubMed:11406349}.
/FTId=VAR_021502.
VARIANT 318 318 G -> R (in GGM; dbSNP:rs371505974).
{ECO:0000269|PubMed:10036327}.
/FTId=VAR_021503.
VARIANT 411 411 A -> T (in dbSNP:rs17683430).
/FTId=VAR_029148.
VARIANT 468 468 A -> V (in GGM; dbSNP:rs200406921).
{ECO:0000269|PubMed:10036327}.
/FTId=VAR_021504.
MUTAGEN 248 248 N->Q: Loss of N-glycosylation.
{ECO:0000269|PubMed:8567640}.
CONFLICT 631 631 K -> R (in Ref. 4; BAH14555).
{ECO:0000305}.
SEQUENCE 664 AA; 73498 MW; 2B403376595EAB74 CRC64;
MDSSTWSPKT TAVTRPVETH ELIRNAADIS IIVIYFVVVM AVGLWAMFST NRGTVGGFFL
AGRSMVWWPI GASLFASNIG SGHFVGLAGT GAASGIAIGG FEWNALVLVV VLGWLFVPIY
IKAGVVTMPE YLRKRFGGQR IQVYLSLLSL LLYIFTKISA DIFSGAIFIN LALGLNLYLA
IFLLLAITAL YTITGGLAAV IYTDTLQTVI MLVGSLILTG FAFHEVGGYD AFMEKYMKAI
PTIVSDGNTT FQEKCYTPRA DSFHIFRDPL TGDLPWPGFI FGMSILTLWY WCTDQVIVQR
CLSAKNMSHV KGGCILCGYL KLMPMFIMVM PGMISRILYT EKIACVVPSE CEKYCGTKVG
CTNIAYPTLV VELMPNGLRG LMLSVMLASL MSSLTSIFNS ASTLFTMDIY AKVRKRASEK
ELMIAGRLFI LVLIGISIAW VPIVQSAQSG QLFDYIQSIT SYLGPPIAAV FLLAIFWKRV
NEPGAFWGLI LGLLIGISRM ITEFAYGTGS CMEPSNCPTI ICGVHYLYFA IILFAISFIT
IVVISLLTKP IPDVHLYRLC WSLRNSKEER IDLDAEEENI QEGPKETIEI ETQVPEKKKG
IFRRAYDLFC GLEQHGAPKM TEEEEKAMKM KMTDTSEKPL WRTVLNVNGI ILVTVAVFCH
AYFA


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U0658r CLIA High affinity sodium-glucose cotransporter,Na(+)_glucose cotransporter 1,Rat,Rattus norvegicus,Sglt1,Slc5a1,Sodium_glucose cotransporter 1,Solute carrier family 5 member 1 96T
E0658r ELISA kit High affinity sodium-glucose cotransporter,Na(+)_glucose cotransporter 1,Rat,Rattus norvegicus,Sglt1,Slc5a1,Sodium_glucose cotransporter 1,Solute carrier family 5 member 1 96T
E0658r ELISA High affinity sodium-glucose cotransporter,Na(+)_glucose cotransporter 1,Rat,Rattus norvegicus,Sglt1,Slc5a1,Sodium_glucose cotransporter 1,Solute carrier family 5 member 1 96T
E0658Rb ELISA kit High affinity sodium-glucose cotransporter,Na(+)_glucose cotransporter 1,Oryctolagus cuniculus,Rabbit,SGLT1,SLC5A1,Sodium_glucose cotransporter 1,Solute carrier family 5 member 1 96T
U0658Rb CLIA High affinity sodium-glucose cotransporter,Na(+)_glucose cotransporter 1,Oryctolagus cuniculus,Rabbit,SGLT1,SLC5A1,Sodium_glucose cotransporter 1,Solute carrier family 5 member 1 96T
E0658Rb ELISA High affinity sodium-glucose cotransporter,Na(+)_glucose cotransporter 1,Oryctolagus cuniculus,Rabbit,SGLT1,SLC5A1,Sodium_glucose cotransporter 1,Solute carrier family 5 member 1 96T
E0658h ELISA kit High affinity sodium-glucose cotransporter,Homo sapiens,Human,Na(+)_glucose cotransporter 1,NAGT,SGLT1,SLC5A1,Sodium_glucose cotransporter 1,Solute carrier family 5 member 1 96T
U0658h CLIA High affinity sodium-glucose cotransporter,Homo sapiens,Human,Na(+)_glucose cotransporter 1,NAGT,SGLT1,SLC5A1,Sodium_glucose cotransporter 1,Solute carrier family 5 member 1 96T
E0658h ELISA High affinity sodium-glucose cotransporter,Homo sapiens,Human,Na(+)_glucose cotransporter 1,NAGT,SGLT1,SLC5A1,Sodium_glucose cotransporter 1,Solute carrier family 5 member 1 96T
EIAAB37424 Low affinity sodium-glucose cotransporter,Mouse,Mus musculus,Na(+)_glucose cotransporter 3,Slc5a4a,Sodium_glucose cotransporter 3,Solute carrier family 5 member 4
EIAAB37423 Low affinity sodium-glucose cotransporter,Na(+)_glucose cotransporter 3,Pig,SAAT1,SGLT3,SLC5A4,Sodium_glucose cotransporter 3,Solute carrier family 5 member 4,Sus scrofa
E0659m ELISA kit Low affinity sodium-glucose cotransporter,Mouse,Mus musculus,Na(+)_glucose cotransporter 2,Sglt2,Slc5a2,Sodium_glucose cotransporter 2,Solute carrier family 5 member 2 96T
U0659r CLIA Low affinity sodium-glucose cotransporter,Na(+)_glucose cotransporter 2,Rat,Rattus norvegicus,Sglt2,Slc5a2,Sodium_glucose cotransporter 2,Solute carrier family 5 member 2 96T
E0659r ELISA kit Low affinity sodium-glucose cotransporter,Na(+)_glucose cotransporter 2,Rat,Rattus norvegicus,Sglt2,Slc5a2,Sodium_glucose cotransporter 2,Solute carrier family 5 member 2 96T
U0659m CLIA Low affinity sodium-glucose cotransporter,Mouse,Mus musculus,Na(+)_glucose cotransporter 2,Sglt2,Slc5a2,Sodium_glucose cotransporter 2,Solute carrier family 5 member 2 96T
E0659m ELISA Low affinity sodium-glucose cotransporter,Mouse,Mus musculus,Na(+)_glucose cotransporter 2,Sglt2,Slc5a2,Sodium_glucose cotransporter 2,Solute carrier family 5 member 2 96T
E0659r ELISA Low affinity sodium-glucose cotransporter,Na(+)_glucose cotransporter 2,Rat,Rattus norvegicus,Sglt2,Slc5a2,Sodium_glucose cotransporter 2,Solute carrier family 5 member 2 96T
E0659h ELISA kit Homo sapiens,Human,Low affinity sodium-glucose cotransporter,Na(+)_glucose cotransporter 2,SGLT2,SLC5A2,Sodium_glucose cotransporter 2,Solute carrier family 5 member 2 96T
EIAAB37422 Homo sapiens,Human,Low affinity sodium-glucose cotransporter,Na(+)_glucose cotransporter 3,SAAT1,SGLT2,SLC5A4,Sodium_glucose cotransporter 3,Solute carrier family 5 member 4


 

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