Did you know ? If you order before Friday 14h we deliver 90PCT of the the time next Tuesday, GENTAUR another in time delivery

CAP-Gly domain-containing linker protein 2 (Cytoplasmic linker protein 115) (CLIP-115) (Cytoplasmic linker protein 2) (Williams-Beuren syndrome chromosomal region 3 protein) (Williams-Beuren syndrome chromosomal region 4 protein)

 CLIP2_HUMAN             Reviewed;        1046 AA.
Q9UDT6; O14527; O43611;
27-SEP-2005, integrated into UniProtKB/Swiss-Prot.
01-MAY-2000, sequence version 1.
12-SEP-2018, entry version 146.
RecName: Full=CAP-Gly domain-containing linker protein 2;
AltName: Full=Cytoplasmic linker protein 115;
Short=CLIP-115;
AltName: Full=Cytoplasmic linker protein 2;
AltName: Full=Williams-Beuren syndrome chromosomal region 3 protein;
AltName: Full=Williams-Beuren syndrome chromosomal region 4 protein;
Name=CLIP2; Synonyms=CYLN2, KIAA0291, WBSCR3, WBSCR4, WSCR4;
Homo sapiens (Human).
Eukaryota; Metazoa; Chordata; Craniata; Vertebrata; Euteleostomi;
Mammalia; Eutheria; Euarchontoglires; Primates; Haplorrhini;
Catarrhini; Hominidae; Homo.
NCBI_TaxID=9606;
[1]
NUCLEOTIDE SEQUENCE [LARGE SCALE MRNA] (ISOFORM 2), AND VARIANT
PRO-977.
TISSUE=Brain;
PubMed=9179496; DOI=10.1093/dnares/4.1.53;
Ohara O., Nagase T., Ishikawa K., Nakajima D., Ohira M., Seki N.,
Nomura N.;
"Construction and characterization of human brain cDNA libraries
suitable for analysis of cDNA clones encoding relatively large
proteins.";
DNA Res. 4:53-59(1997).
[2]
SEQUENCE REVISION.
PubMed=12168954; DOI=10.1093/dnares/9.3.99;
Nakajima D., Okazaki N., Yamakawa H., Kikuno R., Ohara O., Nagase T.;
"Construction of expression-ready cDNA clones for KIAA genes: manual
curation of 330 KIAA cDNA clones.";
DNA Res. 9:99-106(2002).
[3]
NUCLEOTIDE SEQUENCE [LARGE SCALE GENOMIC DNA].
PubMed=12853948; DOI=10.1038/nature01782;
Hillier L.W., Fulton R.S., Fulton L.A., Graves T.A., Pepin K.H.,
Wagner-McPherson C., Layman D., Maas J., Jaeger S., Walker R.,
Wylie K., Sekhon M., Becker M.C., O'Laughlin M.D., Schaller M.E.,
Fewell G.A., Delehaunty K.D., Miner T.L., Nash W.E., Cordes M., Du H.,
Sun H., Edwards J., Bradshaw-Cordum H., Ali J., Andrews S., Isak A.,
Vanbrunt A., Nguyen C., Du F., Lamar B., Courtney L., Kalicki J.,
Ozersky P., Bielicki L., Scott K., Holmes A., Harkins R., Harris A.,
Strong C.M., Hou S., Tomlinson C., Dauphin-Kohlberg S.,
Kozlowicz-Reilly A., Leonard S., Rohlfing T., Rock S.M.,
Tin-Wollam A.-M., Abbott A., Minx P., Maupin R., Strowmatt C.,
Latreille P., Miller N., Johnson D., Murray J., Woessner J.P.,
Wendl M.C., Yang S.-P., Schultz B.R., Wallis J.W., Spieth J.,
Bieri T.A., Nelson J.O., Berkowicz N., Wohldmann P.E., Cook L.L.,
Hickenbotham M.T., Eldred J., Williams D., Bedell J.A., Mardis E.R.,
Clifton S.W., Chissoe S.L., Marra M.A., Raymond C., Haugen E.,
Gillett W., Zhou Y., James R., Phelps K., Iadanoto S., Bubb K.,
Simms E., Levy R., Clendenning J., Kaul R., Kent W.J., Furey T.S.,
Baertsch R.A., Brent M.R., Keibler E., Flicek P., Bork P., Suyama M.,
Bailey J.A., Portnoy M.E., Torrents D., Chinwalla A.T., Gish W.R.,
Eddy S.R., McPherson J.D., Olson M.V., Eichler E.E., Green E.D.,
Waterston R.H., Wilson R.K.;
"The DNA sequence of human chromosome 7.";
Nature 424:157-164(2003).
[4]
NUCLEOTIDE SEQUENCE [GENOMIC DNA] OF 42-460.
PubMed=8812460; DOI=10.1006/geno.1996.0469;
Osborne L.R., Martindale D.W., Scherer S.W., Shi X.-M., Huizenga J.,
Heng H.H.Q., Costa T., Pober B., Lew L., Brinkman J., Rommens J.,
Koop B.F., Tsui L.-C.;
"Identification of genes from a 500-kb region at 7q11.23 that is
commonly deleted in Williams syndrome patients.";
Genomics 36:328-336(1996).
[5]
PROTEIN SEQUENCE OF 350-362 AND 689-701, AND IDENTIFICATION BY MASS
SPECTROMETRY.
TISSUE=Fetal brain cortex;
Lubec G., Chen W.-Q., Sun Y.;
Submitted (DEC-2008) to UniProtKB.
[6]
GENE STRUCTURE.
PubMed=9799601; DOI=10.1006/geno.1998.5529;
Hoogenraad C.C., Eussen B.H.J., Langeveld A., van Haperen R.,
Winterberg S., Wouters C.H., Grosveld F., de Zeeuw C.I., Galjart N.;
"The murine CYLN2 gene: genomic organization, chromosome localization,
and comparison to the human gene that is located within the 7q11.23
Williams syndrome critical region.";
Genomics 53:348-358(1998).
[7]
INTERACTION WITH CLASP1 AND CLASP2.
PubMed=11290329; DOI=10.1016/S0092-8674(01)00288-4;
Akhmanova A., Hoogenraad C.C., Drabek K., Stepanova T., Dortland B.,
Verkerk T., Vermeulen W., Burgering B.M., de Zeeuw C.I., Grosveld F.,
Galjart N.;
"Clasps are CLIP-115 and -170 associating proteins involved in the
regional regulation of microtubule dynamics in motile fibroblasts.";
Cell 104:923-935(2001).
[8]
IDENTIFICATION BY MASS SPECTROMETRY [LARGE SCALE ANALYSIS].
TISSUE=Platelet;
PubMed=18088087; DOI=10.1021/pr0704130;
Zahedi R.P., Lewandrowski U., Wiesner J., Wortelkamp S., Moebius J.,
Schuetz C., Walter U., Gambaryan S., Sickmann A.;
"Phosphoproteome of resting human platelets.";
J. Proteome Res. 7:526-534(2008).
[9]
IDENTIFICATION BY MASS SPECTROMETRY [LARGE SCALE ANALYSIS].
PubMed=21269460; DOI=10.1186/1752-0509-5-17;
Burkard T.R., Planyavsky M., Kaupe I., Breitwieser F.P.,
Buerckstuemmer T., Bennett K.L., Superti-Furga G., Colinge J.;
"Initial characterization of the human central proteome.";
BMC Syst. Biol. 5:17-17(2011).
[10]
INVOLVEMENT IN WBS.
PubMed=22608712; DOI=10.1016/j.ajhg.2012.04.020;
Vandeweyer G., Van der Aa N., Reyniers E., Kooy R.F.;
"The contribution of CLIP2 haploinsufficiency to the clinical
manifestations of the Williams-Beuren syndrome.";
Am. J. Hum. Genet. 90:1071-1078(2012).
[11]
PHOSPHORYLATION [LARGE SCALE ANALYSIS] AT SER-923, AND IDENTIFICATION
BY MASS SPECTROMETRY [LARGE SCALE ANALYSIS].
TISSUE=Cervix carcinoma, and Erythroleukemia;
PubMed=23186163; DOI=10.1021/pr300630k;
Zhou H., Di Palma S., Preisinger C., Peng M., Polat A.N., Heck A.J.,
Mohammed S.;
"Toward a comprehensive characterization of a human cancer cell
phosphoproteome.";
J. Proteome Res. 12:260-271(2013).
[12]
IDENTIFICATION BY MASS SPECTROMETRY [LARGE SCALE ANALYSIS].
TISSUE=Liver;
PubMed=24275569; DOI=10.1016/j.jprot.2013.11.014;
Bian Y., Song C., Cheng K., Dong M., Wang F., Huang J., Sun D.,
Wang L., Ye M., Zou H.;
"An enzyme assisted RP-RPLC approach for in-depth analysis of human
liver phosphoproteome.";
J. Proteomics 96:253-262(2014).
[13]
STRUCTURE BY NMR OF 68-149 AND 219-289.
RIKEN structural genomics initiative (RSGI);
"Solution structure of the 1st and 2nd CAP-Gly domain in human CLIP-
115/CYLN2.";
Submitted (NOV-2005) to the PDB data bank.
-!- FUNCTION: Seems to link microtubules to dendritic lamellar body
(DLB), a membranous organelle predominantly present in bulbous
dendritic appendages of neurons linked by dendrodendritic gap
junctions. May operate in the control of brain-specific organelle
translocations (By similarity). {ECO:0000250}.
-!- SUBUNIT: Interacts with CLASP1 and CLASP2 (PubMed:11290329). Binds
preferentially to tyrosinated microtubules, and only marginally to
detyrosinated microtubules (By similarity).
{ECO:0000250|UniProtKB:Q9Z0H8, ECO:0000269|PubMed:11290329}.
-!- SUBCELLULAR LOCATION: Cytoplasm {ECO:0000250|UniProtKB:O55156}.
Cytoplasm, cytoskeleton {ECO:0000250|UniProtKB:Q9Z0H8}.
Note=Localizes preferentially to the ends of tyrosinated
microtubules. {ECO:0000250|UniProtKB:Q9Z0H8}.
-!- ALTERNATIVE PRODUCTS:
Event=Alternative splicing; Named isoforms=2;
Name=1;
IsoId=Q9UDT6-1; Sequence=Displayed;
Name=2;
IsoId=Q9UDT6-2; Sequence=VSP_015682;
-!- DISEASE: Note=CLIP2 is located in the Williams-Beuren syndrome
(WBS) critical region (PubMed:9799601). WBS results from a
hemizygous deletion of several genes on chromosome 7q11.23,
thought to arise as a consequence of unequal crossing over between
highly homologous low-copy repeat sequences flanking the deleted
region. Haploinsufficiency of CLIP2 may be the cause of certain
cardiovascular and musculo-skeletal abnormalities observed in the
disease. However, it has been demonstrated that haploinsufficiency
of this gene alone is not sufficient to cause any of the cognitive
or facial features of WBS (PubMed:22608712).
{ECO:0000305|PubMed:22608712, ECO:0000305|PubMed:9799601}.
-!- SEQUENCE CAUTION:
Sequence=BAA22960.2; Type=Erroneous initiation; Evidence={ECO:0000305};
-----------------------------------------------------------------------
Copyrighted by the UniProt Consortium, see https://www.uniprot.org/terms
Distributed under the Creative Commons Attribution (CC BY 4.0) License
-----------------------------------------------------------------------
EMBL; AB006629; BAA22960.2; ALT_INIT; mRNA.
EMBL; AC005015; AAF03524.1; -; Genomic_DNA.
EMBL; AF041059; AAB96784.1; -; Genomic_DNA.
EMBL; AF041055; AAB96784.1; JOINED; Genomic_DNA.
EMBL; AF041056; AAB96784.1; JOINED; Genomic_DNA.
EMBL; AF041057; AAB96784.1; JOINED; Genomic_DNA.
EMBL; AF041058; AAB96784.1; JOINED; Genomic_DNA.
CCDS; CCDS5569.1; -. [Q9UDT6-1]
CCDS; CCDS5570.1; -. [Q9UDT6-2]
RefSeq; NP_003379.3; NM_003388.4.
RefSeq; NP_115797.1; NM_032421.2.
UniGene; Hs.647018; -.
PDB; 2CP2; NMR; -; A=68-149.
PDB; 2CP3; NMR; -; A=219-289.
PDBsum; 2CP2; -.
PDBsum; 2CP3; -.
ProteinModelPortal; Q9UDT6; -.
SMR; Q9UDT6; -.
BioGrid; 113300; 11.
IntAct; Q9UDT6; 9.
STRING; 9606.ENSP00000223398; -.
CarbonylDB; Q9UDT6; -.
iPTMnet; Q9UDT6; -.
PhosphoSitePlus; Q9UDT6; -.
SwissPalm; Q9UDT6; -.
BioMuta; CLIP2; -.
DMDM; 74753268; -.
EPD; Q9UDT6; -.
PaxDb; Q9UDT6; -.
PeptideAtlas; Q9UDT6; -.
PRIDE; Q9UDT6; -.
ProteomicsDB; 84116; -.
ProteomicsDB; 84117; -. [Q9UDT6-2]
DNASU; 7461; -.
Ensembl; ENST00000223398; ENSP00000223398; ENSG00000106665. [Q9UDT6-1]
Ensembl; ENST00000361545; ENSP00000355151; ENSG00000106665. [Q9UDT6-2]
Ensembl; ENST00000395060; ENSP00000378500; ENSG00000106665. [Q9UDT6-1]
GeneID; 7461; -.
KEGG; hsa:7461; -.
UCSC; uc003uam.3; human. [Q9UDT6-1]
CTD; 7461; -.
DisGeNET; 7461; -.
EuPathDB; HostDB:ENSG00000106665.15; -.
GeneCards; CLIP2; -.
HGNC; HGNC:2586; CLIP2.
HPA; CAB020767; -.
HPA; HPA020430; -.
MalaCards; CLIP2; -.
MIM; 603432; gene.
neXtProt; NX_Q9UDT6; -.
OpenTargets; ENSG00000106665; -.
Orphanet; 904; Williams syndrome.
PharmGKB; PA27085; -.
eggNOG; KOG4568; Eukaryota.
eggNOG; COG5244; LUCA.
GeneTree; ENSGT00760000119173; -.
HOGENOM; HOG000092755; -.
HOVERGEN; HBG007123; -.
InParanoid; Q9UDT6; -.
KO; K10422; -.
OMA; NLRAKHD; -.
OrthoDB; EOG091G0J1Y; -.
PhylomeDB; Q9UDT6; -.
TreeFam; TF326096; -.
ChiTaRS; CLIP2; human.
EvolutionaryTrace; Q9UDT6; -.
GeneWiki; CLIP2; -.
GenomeRNAi; 7461; -.
PRO; PR:Q9UDT6; -.
Proteomes; UP000005640; Chromosome 7.
Bgee; ENSG00000106665; Expressed in 184 organ(s), highest expression level in frontal cortex.
CleanEx; HS_CLIP2; -.
ExpressionAtlas; Q9UDT6; baseline and differential.
Genevisible; Q9UDT6; HS.
GO; GO:0005881; C:cytoplasmic microtubule; IEA:Ensembl.
GO; GO:0005875; C:microtubule associated complex; TAS:ProtInc.
GO; GO:0035371; C:microtubule plus-end; ISS:UniProtKB.
GO; GO:0008017; F:microtubule binding; ISS:UniProtKB.
GO; GO:0051010; F:microtubule plus-end binding; IEA:Ensembl.
Gene3D; 2.30.30.190; -; 2.
InterPro; IPR036859; CAP-Gly_dom_sf.
InterPro; IPR000938; CAP-Gly_domain.
InterPro; IPR028394; CLIP2.
PANTHER; PTHR18916:SF10; PTHR18916:SF10; 1.
Pfam; PF01302; CAP_GLY; 2.
SMART; SM01052; CAP_GLY; 2.
SUPFAM; SSF74924; SSF74924; 2.
PROSITE; PS00845; CAP_GLY_1; 2.
PROSITE; PS50245; CAP_GLY_2; 2.
1: Evidence at protein level;
3D-structure; Alternative splicing; Coiled coil; Complete proteome;
Cytoplasm; Cytoskeleton; Direct protein sequencing; Microtubule;
Phosphoprotein; Polymorphism; Reference proteome; Repeat;
Williams-Beuren syndrome.
CHAIN 1 1046 CAP-Gly domain-containing linker protein
2.
/FTId=PRO_0000083515.
DOMAIN 99 141 CAP-Gly 1. {ECO:0000255|PROSITE-
ProRule:PRU00045}.
DOMAIN 239 281 CAP-Gly 2. {ECO:0000255|PROSITE-
ProRule:PRU00045}.
COILED 354 524 {ECO:0000255}.
COILED 561 636 {ECO:0000255}.
COILED 673 1016 {ECO:0000255}.
COMPBIAS 314 345 Ser-rich.
MOD_RES 49 49 Phosphoserine.
{ECO:0000250|UniProtKB:Q9Z0H8}.
MOD_RES 202 202 Phosphoserine.
{ECO:0000250|UniProtKB:O55156}.
MOD_RES 207 207 Phosphoserine.
{ECO:0000250|UniProtKB:Q9Z0H8}.
MOD_RES 211 211 Phosphoserine.
{ECO:0000250|UniProtKB:Q9Z0H8}.
MOD_RES 314 314 Phosphoserine.
{ECO:0000250|UniProtKB:Q9Z0H8}.
MOD_RES 923 923 Phosphoserine.
{ECO:0000244|PubMed:23186163}.
MOD_RES 973 973 Phosphoserine.
{ECO:0000250|UniProtKB:Q9Z0H8}.
MOD_RES 979 979 Phosphoserine.
{ECO:0000250|UniProtKB:Q9Z0H8}.
VAR_SEQ 461 495 Missing (in isoform 2).
{ECO:0000303|PubMed:9179496}.
/FTId=VSP_015682.
VARIANT 961 961 D -> E (in dbSNP:rs17145468).
/FTId=VAR_055636.
VARIANT 977 977 R -> P (in dbSNP:rs2522943).
{ECO:0000269|PubMed:9179496}.
/FTId=VAR_023618.
STRAND 73 75 {ECO:0000244|PDB:2CP2}.
STRAND 84 86 {ECO:0000244|PDB:2CP2}.
HELIX 87 89 {ECO:0000244|PDB:2CP2}.
STRAND 92 100 {ECO:0000244|PDB:2CP2}.
STRAND 102 104 {ECO:0000244|PDB:2CP2}.
STRAND 106 116 {ECO:0000244|PDB:2CP2}.
STRAND 118 124 {ECO:0000244|PDB:2CP2}.
TURN 134 136 {ECO:0000244|PDB:2CP2}.
STRAND 137 140 {ECO:0000244|PDB:2CP2}.
HELIX 142 144 {ECO:0000244|PDB:2CP2}.
STRAND 224 227 {ECO:0000244|PDB:2CP3}.
TURN 228 230 {ECO:0000244|PDB:2CP3}.
STRAND 231 240 {ECO:0000244|PDB:2CP3}.
STRAND 242 256 {ECO:0000244|PDB:2CP3}.
STRAND 259 264 {ECO:0000244|PDB:2CP3}.
STRAND 267 270 {ECO:0000244|PDB:2CP3}.
TURN 274 276 {ECO:0000244|PDB:2CP3}.
STRAND 277 281 {ECO:0000244|PDB:2CP3}.
HELIX 282 284 {ECO:0000244|PDB:2CP3}.
STRAND 285 287 {ECO:0000244|PDB:2CP3}.
SEQUENCE 1046 AA; 115837 MW; 7A0B3C796E1C6E25 CRC64;
MQKPSGLKPP GRGGKHSSPM GRTSTGSASS SAAVAASSKE GSPLHKQSSG PSSSPAAAAA
PEKPGPKAAE VGDDFLGDFV VGERVWVNGV KPGVVQYLGE TQFAPGQWAG VVLDDPVGKN
DGAVGGVRYF ECPALQGIFT RPSKLTRQPT AEGSGSDAHS VESLTAQNLS LHSGTATPPL
TSRVIPLRES VLNSSVKTGN ESGSNLSDSG SVKRGEKDLR LGDRVLVGGT KTGVVRYVGE
TDFAKGEWCG VELDEPLGKN DGAVAGTRYF QCPPKFGLFA PIHKVIRIGF PSTSPAKAKK
TKRMAMGVSA LTHSPSSSSI SSVSSVASSV GGRPSRSGLL TETSSRYARK ISGTTALQEA
LKEKQQHIEQ LLAERDLERA EVAKATSHIC EVEKEIALLK AQHEQYVAEA EEKLQRARLL
VESVRKEKVD LSNQLEEERR KVEDLQFRVE EESITKGDLE TQTQLEHARI GELEQSLLLE
KAQAERLLRE LADNRLTTVA EKSRVLQLEE ELTLRRGEIE ELQQCLLHSG PPPPDHPDAA
EILRLRERLL SASKEHQRES GVLRDKYEKA LKAYQAEVDK LRAANEKYAQ EVAGLKDKVQ
QATSENMGLM DNWKSKLDSL ASDHQKSLED LKATLNSGPG AQQKEIGELK AVMEGIKMEH
QLELGNLQAK HDLETAMHVK EKEALREKLQ EAQEELAGLQ RHWRAQLEVQ ASQHRLELQE
AQDQRRDAEL RVHELEKLDV EYRGQAQAIE FLKEQISLAE KKMLDYERLQ RAEAQGKQEV
ESLREKLLVA ENRLQAVEAL CSSQHTHMIE SNDISEETIR TKETVEGLQD KLNKRDKEVT
ALTSQTEMLR AQVSALESKC KSGEKKVDAL LKEKRRLEAE LETVSRKTHD ASGQLVLISQ
ELLRKERSLN ELRVLLLEAN RHSPGPERDL SREVHKAEWR IKEQKLKDDI RGLREKLTGL
DKEKSLSDQR RYSLIDRSSA PELLRLQHQL MSTEDALRDA LDQAQQVEKL MEAMRSCPDK
AQTIGNSGSA NGIHQQDKAQ KQEDKH


Related products :

Catalog number Product name Quantity
EIAAB07913 CAP-Gly domain-containing linker protein 2,CLIP-115,CLIP2,CYLN2,Cytoplasmic linker protein 115,Cytoplasmic linker protein 2,Homo sapiens,Human,KIAA0291,WBSCR3,WBSCR4,Williams-Beuren syndrome chromosom
CN043_HUMAN Mouse ELISA Kit FOR Williams-Beuren syndrome chromosomal region 16 protein homolog 96T
I2784 Williams-Beuren syndrome chromosomal region 16 protein (WBSCR16), Mouse, ELISA Kit 96T
I2783 Williams-Beuren syndrome chromosomal region 16 protein (WBSCR16), Human, ELISA Kit 96T
CSB-EL014645MO Mouse Williams-Beuren syndrome chromosomal region 14 protein(MLXIPL) ELISA kit 96T
I2782 Williams-Beuren syndrome chromosomal region 14 protein (MLXIPL), Mouse, ELISA Kit 96T
I2781 Williams-Beuren syndrome chromosomal region 14 protein (MLXIPL), Human, ELISA Kit 96T
E0355p Mouse ELISA Kit FOR Williams-Beuren syndrome chromosomal region 16 protein homolog 96T
CSB-EL025989BO Bovine Williams-Beuren syndrome chromosomal region 28 protein(WBSCR28) ELISA kit 96T
HXA5_RAT Mouse ELISA Kit FOR Williams-Beuren syndrome chromosomal region 16 protein homolog 96T
CSB-EL025989MO Mouse Williams-Beuren syndrome chromosomal region 28 protein(WBSCR28) ELISA kit 96T
I2785 Williams-Beuren syndrome chromosomal region 27 protein (WBSCR27), Human, ELISA Kit 96T
WBS23_HUMAN Human ELISA Kit FOR Putative Williams-Beuren syndrome chromosomal region 23 protein 96T
CSB-EL014645HU Human Williams-Beuren syndrome chromosomal region 14 protein(MLXIPL) ELISA kit 96T
CSB-EL025981HU Human Williams-Beuren syndrome chromosomal region 16 protein(WBSCR16) ELISA kit 96T
CSB-EL025989HU Human Williams-Beuren syndrome chromosomal region 28 protein(WBSCR28) ELISA kit 96T
I2788 Williams-Beuren syndrome chromosomal region 28 protein (WBSCR28), Mouse, ELISA Kit 96T
CSB-EL025981MO Mouse Williams-Beuren syndrome chromosomal region 16 protein(WBSCR16) ELISA kit 96T
I2787 Williams-Beuren syndrome chromosomal region 28 protein (WBSCR28), Human, ELISA Kit 96T
I2786 Williams-Beuren syndrome chromosomal region 28 protein (WBSCR28), Bovine, ELISA Kit 96T
CSB-EL025988HU Human Williams-Beuren syndrome chromosomal region 27 protein(WBSCR27) ELISA kit 96T
EIAAB39474 Homo sapiens,Human,SPDYE1,Speedy protein E1,WBSCR19,Williams-Beuren syndrome chromosomal region 19 protein
EIAAB46112 Homo sapiens,Human,RCC1-like G exchanging factor-like protein,WBSCR16,Williams-Beuren syndrome chromosomal region 16 protein
CSB-EL025989MO Mouse Williams-Beuren syndrome chromosomal region 28 protein(WBSCR28) ELISA kit SpeciesMouse 96T
EIAAB46111 Mouse,Mus musculus,Wbscr16,Williams-Beuren syndrome chromosomal region 16 protein homolog


 

GENTAUR Belgium BVBA BE0473327336
Voortstraat 49, 1910 Kampenhout BELGIUM
Tel 0032 16 58 90 45

Fax 0032 16 50 90 45
info@gentaur.com | Gentaur





GENTAUR Ltd.
Howard Frank Turnberry House
1404-1410 High Road
Whetstone London N20 9BH
Tel 020 3393 8531 Fax 020 8445 9411
uk@gentaur.com | Gentaur

 

 




GENTAUR France SARL
9, rue Lagrange, 75005 Paris
Tel 01 43 25 01 50

Fax 01 43 25 01 60
RCS Paris B 484 237 888

SIRET 48423788800017

BNP PARIBAS PARIS PL MAUBERT BIC BNPAFRPPPRG

france@gentaur.com | Gentaur

GENTAUR GmbH
Marienbongard 20
52062 Aachen Deutschland
Support Karolina Elandt
Tel: 0035929830070
Fax: (+49) 241 56 00 47 88

Logistic :0241 40 08 90 86
Bankleitzahl 39050000
IBAN lautet DE8839050000107569353
Handelsregister Aachen HR B 16058
Umsatzsteuer-Identifikationsnummer *** DE 815175831
Steuernummer 201/5961/3925
de@gentaur.com | Gentaur

GENTAUR U.S.A
Genprice Inc, Logistics
547, Yurok Circle
San Jose, CA 95123
CA 95123
Tel (408) 780-0908,
Fax (408) 780-0908,
sales@genprice.com

Genprice Inc, Invoices and accounting
6017 Snell Ave, Ste 357
San Jose, CA 95123




GENTAUR Nederland BV
NL850396268B01 KVK nummer 52327027
Kuiper 1
5521 DG Eersel Nederland
Tel:  0208-080893  Fax: 0497-517897
nl@gentaur.com | Gentaur
IBAN: NL04 RABO 0156 9854 62   SWIFT RABONL2U






GENTAUR Spain
tel:0911876558
spain@gentaur.com | Gentaur






ГЕНТАУЪР БЪЛГАРИЯ
ID # 201 358 931 /BULSTAT
София 1000, ул. "Граф Игнатиев" 53 вх. В, ет. 2
Tel 0035924682280 Fax 0035924808322
e-mail: Sofia@gentaur.com | Gentaur
IBAN: BG11FINV91501014771636
BIC: FINVBGSF

GENTAUR Poland Sp. z o.o.


ul. Grunwaldzka 88/A m.2
81-771 Sopot, Poland
TEL Gdansk 058 710 33 44 FAX  058 710 33 48              

poland@gentaur.com | Gentaur

Other countries

Österreich +43720880899

Canada Montreal +15149077481

Ceská republika Praha +420246019719

Danmark +4569918806

Finland Helsset +358942419041

Magyarország Budapest +3619980547

Ireland Dublin+35316526556

Luxembourg+35220880274

Norge Oslo+4721031366

Sverige Stockholm+46852503438

Schweiz Züri+41435006251

US New York+17185132983

GENTAUR Italy
SRL IVA IT03841300167
Piazza Giacomo Matteotti, 6
24122 Bergamo Tel 02 36 00 65 93
Fax 02 36 00 65 94
italia@gentaur.com | Gentaur