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Keratin, type I cytoskeletal 12 (Cytokeratin-12) (CK-12) (Keratin-12) (K12)

 K1C12_HUMAN             Reviewed;         494 AA.
Q99456; B2R9E0;
01-NOV-1997, integrated into UniProtKB/Swiss-Prot.
01-MAY-1997, sequence version 1.
20-JUN-2018, entry version 158.
RecName: Full=Keratin, type I cytoskeletal 12;
AltName: Full=Cytokeratin-12;
Short=CK-12;
AltName: Full=Keratin-12;
Short=K12;
Name=KRT12;
Homo sapiens (Human).
Eukaryota; Metazoa; Chordata; Craniata; Vertebrata; Euteleostomi;
Mammalia; Eutheria; Euarchontoglires; Primates; Haplorrhini;
Catarrhini; Hominidae; Homo.
NCBI_TaxID=9606;
[1]
NUCLEOTIDE SEQUENCE [MRNA], AND TISSUE SPECIFICITY.
TISSUE=Cornea;
PubMed=8759347;
Nishida K., Adachi W., Shimizu-Matsumoto A., Kinoshita S., Mizuno K.,
Matsubara K., Okubo K.;
"A gene expression profile of human corneal epithelium and the
isolation of human keratin 12 cDNA.";
Invest. Ophthalmol. Vis. Sci. 37:1800-1809(1996).
[2]
NUCLEOTIDE SEQUENCE [GENOMIC DNA], AND VARIANTS MECD GLY-135; ILE-135;
ARG-140 AND ASP-429.
PubMed=9399908; DOI=10.1086/301650;
Nishida K., Honma Y., Dota A., Kawasaki S., Adachi W., Nakamura T.,
Quantock A.J., Hosotani H., Yamamoto S., Okada M., Shimomura Y.,
Kinoshita S.;
"Isolation and chromosomal localization of a cornea-specific human
keratin 12 gene and detection of four mutations in Meesmann corneal
epithelial dystrophy.";
Am. J. Hum. Genet. 61:1268-1275(1997).
[3]
NUCLEOTIDE SEQUENCE [MRNA], VARIANTS MECD THR-129 AND THR-135, AND
VARIANT TRP-20.
PubMed=10644419; DOI=10.1006/exer.1999.0769;
Corden L.D., Swensson O., Swensson B., Smith F.J.D., Rochels R.,
Uitto J., McLean W.H.I.;
"Molecular genetics of Meesmann's corneal dystrophy: ancestral and
novel mutations in keratin 12 (K12) and complete sequence of the human
KRT12 gene.";
Exp. Eye Res. 70:41-49(2000).
[4]
NUCLEOTIDE SEQUENCE [LARGE SCALE MRNA].
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].
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.
[6]
PROTEIN SEQUENCE OF 21-31.
TISSUE=Platelet;
PubMed=12665801; DOI=10.1038/nbt810;
Gevaert K., Goethals M., Martens L., Van Damme J., Staes A.,
Thomas G.R., Vandekerckhove J.;
"Exploring proteomes and analyzing protein processing by mass
spectrometric identification of sorted N-terminal peptides.";
Nat. Biotechnol. 21:566-569(2003).
[7]
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).
[8]
VARIANTS MECD THR-135 AND LEU-143.
PubMed=9171831; DOI=10.1038/ng0697-184;
Irvine A.D., Corden L.D., Swensson O., Swensson B., Moore J.E.,
Frazer D.G., Smith F.J.D., Knowlton R.G., Christophers E., Rochels R.,
Uitto J., McLean W.H.I.;
"Mutations in cornea-specific keratin K3 or K12 genes cause Meesmann's
corneal dystrophy.";
Nat. Genet. 16:184-187(1997).
[9]
VARIANT MECD PRO-130.
PubMed=10781519; DOI=10.1136/bjo.84.5.527;
Corden L.D., Swensson O., Swensson B., Rochels R., Wannke B.,
Thiel H.J., McLean W.H.I.;
"A novel keratin 12 mutation in a German kindred with Meesmann's
corneal dystrophy.";
Br. J. Ophthalmol. 84:527-530(2000).
[10]
VARIANT MECD PRO-137.
PubMed=12543196; DOI=10.1016/S0021-5155(02)00563-4;
Takahashi K., Takahashi K., Murakami A., Okisaka S., Kimura T.,
Kanai A.;
"Heterozygous Ala137Pro mutation in keratin 12 gene found in Japanese
with Meesmann's corneal dystrophy.";
Jpn. J. Ophthalmol. 46:673-674(2002).
[11]
VARIANTS MECD SER-135 AND ILE-SER-ASN-LEU-GLU-ALA-GLN-LEU-LEU-399 INS.
PubMed=15148206; DOI=10.1136/bjo.2003.032870;
Yoon M.K., Warren J.F., Holsclaw D.S., Gritz D.C., Margolis T.P.;
"A novel arginine substitution mutation in 1A domain and a novel 27 bp
insertion mutation in 2B domain of keratin 12 gene associated with
Meesmann's corneal dystrophy.";
Br. J. Ophthalmol. 88:752-756(2004).
[12]
VARIANT MECD CYS-429.
PubMed=16227835; DOI=10.1097/01.ico.0000159732.29930.26;
Chen Y.T., Tseng S.H., Chao S.C.;
"Novel mutations in the helix termination motif of keratin 3 and
keratin 12 in 2 Taiwanese families with Meesmann corneal dystrophy.";
Cornea 24:928-932(2005).
[13]
VARIANTS MECD THR-129 AND SER-426.
PubMed=16352477; DOI=10.1080/13816810500374391;
Nichini O., Manzi V., Munier F.L., Schorderet D.F.;
"Meesmann corneal dystrophy (MECD): report of 2 families and a novel
mutation in the cornea specific keratin 12 (KRT12) gene.";
Ophthalmic Genet. 26:169-173(2005).
[14]
VARIANT MECD PRO-430.
PubMed=17653038;
Sullivan L.S., Baylin E.B., Font R., Daiger S.P., Pepose J.S.,
Clinch T.E., Nakamura H., Zhao X.C., Yee R.W.;
"A novel mutation of the Keratin 12 gene responsible for a severe
phenotype of Meesmann's corneal dystrophy.";
Mol. Vis. 13:975-980(2007).
[15]
VARIANTS SER-15 AND TRP-20, AND VARIANT MECD LEU-143.
PubMed=18245975; DOI=10.1097/ICO.0b013e31815652fd;
Nielsen K., Orntoft T., Hjortdal J., Rasmussen T., Ehlers N.;
"A novel mutation as the basis for asymptomatic meesmann dystrophy in
a Danish family.";
Cornea 27:100-102(2008).
[16]
VARIANT MECD ARG-433.
PubMed=18661274; DOI=10.1007/s10384-007-0518-2;
Seto T., Fujiki K., Kishishita H., Fujimaki T., Murakami A., Kanai A.;
"A novel mutation in the cornea-specific keratin 12 gene in Meesmann
corneal dystrophy.";
Jpn. J. Ophthalmol. 52:224-226(2008).
[17]
VARIANT SER-15, AND VARIANT MECD VAL-129.
PubMed=20577595;
Clausen I., Duncker G.I., Grunauer-Kloevekorn C.;
"Identification of a novel mutation in the cornea specific keratin 12
gene causing Meesmann's corneal dystrophy in a German family.";
Mol. Vis. 16:954-960(2010).
[18]
VARIANT MECD PRO-132.
PubMed=23222558; DOI=10.1038/eye.2012.261;
Hassan H., Thaung C., Ebenezer N.D., Larkin G., Hardcastle A.J.,
Tuft S.J.;
"Severe Meesmann's epithelial corneal dystrophy phenotype due to a
missense mutation in the helix-initiation motif of keratin 12.";
Eye 27:367-373(2013).
[19]
VARIANT MECD GLN-140.
PubMed=24099278; DOI=10.1016/j.ajo.2013.08.008;
Ogasawara M., Matsumoto Y., Hayashi T., Ohno K., Yamada H.,
Kawakita T., Dogru M., Shimazaki J., Tsubota K., Tsuneoka H.;
"KRT12 mutations and in vivo confocal microscopy in two Japanese
families with Meesmann corneal dystrophy.";
Am. J. Ophthalmol. 157:93-102(2014).
-!- FUNCTION: May play a unique role in maintaining the normal corneal
epithelial function. Together with KRT3, essential for the
maintenance of corneal epithelium integrity (By similarity).
{ECO:0000250}.
-!- SUBUNIT: Heterotetramer of two type I and two type II keratins.
Keratin-3 associates with keratin-12.
-!- TISSUE SPECIFICITY: Cornea specific. {ECO:0000269|PubMed:8759347}.
-!- DISEASE: Corneal dystrophy, Meesmann (MECD) [MIM:122100]: An
autosomal dominant corneal disease characterized by fragility of
the anterior corneal epithelium. Patients are usually asymptomatic
until adulthood when rupture of the corneal microcysts may cause
erosions, producing clinical symptoms such as photophobia, contact
lens intolerance and intermittent diminution of visual acuity.
Rarely, subepithelial scarring causes irregular corneal
astigmatism and permanent visual impairment. Histological
examination shows a disorganized and thickened epithelium with
widespread cytoplasmic vacuolation and numerous small, round,
debris-laden intraepithelial cysts. {ECO:0000269|PubMed:10644419,
ECO:0000269|PubMed:10781519, ECO:0000269|PubMed:12543196,
ECO:0000269|PubMed:15148206, ECO:0000269|PubMed:16227835,
ECO:0000269|PubMed:16352477, ECO:0000269|PubMed:17653038,
ECO:0000269|PubMed:18245975, ECO:0000269|PubMed:18661274,
ECO:0000269|PubMed:20577595, ECO:0000269|PubMed:23222558,
ECO:0000269|PubMed:24099278, ECO:0000269|PubMed:9171831,
ECO:0000269|PubMed:9399908}. Note=The disease is caused by
mutations affecting the gene represented in this entry.
-!- MISCELLANEOUS: There are two types of cytoskeletal and
microfibrillar keratin: I (acidic; 40-55 kDa) and II (neutral to
basic; 56-70 kDa).
-!- SIMILARITY: Belongs to the intermediate filament family.
{ECO:0000255|PROSITE-ProRule:PRU01188}.
-!- WEB RESOURCE: Name=Human Intermediate Filament Mutation Database;
URL="http://www.interfil.org";
-!- WEB RESOURCE: Name=Wikipedia; Note=Keratin-12 entry;
URL="https://en.wikipedia.org/wiki/Keratin_12";
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EMBL; D78367; BAA11376.1; -; mRNA.
EMBL; AB007119; BAA25063.1; -; Genomic_DNA.
EMBL; AF137286; AAF61432.1; -; Genomic_DNA.
EMBL; AK313747; BAG36487.1; -; mRNA.
EMBL; CH471152; EAW60685.1; -; Genomic_DNA.
CCDS; CCDS11378.1; -.
RefSeq; NP_000214.1; NM_000223.3.
UniGene; Hs.66739; -.
ProteinModelPortal; Q99456; -.
SMR; Q99456; -.
BioGrid; 110057; 4.
STRING; 9606.ENSP00000251643; -.
DrugBank; DB00400; Griseofulvin.
iPTMnet; Q99456; -.
PhosphoSitePlus; Q99456; -.
SwissPalm; Q99456; -.
BioMuta; KRT12; -.
DMDM; 2497269; -.
PaxDb; Q99456; -.
PeptideAtlas; Q99456; -.
PRIDE; Q99456; -.
ProteomicsDB; 78275; -.
DNASU; 3859; -.
Ensembl; ENST00000251643; ENSP00000251643; ENSG00000187242.
Ensembl; ENST00000572470; ENSP00000459559; ENSG00000263243.
GeneID; 3859; -.
KEGG; hsa:3859; -.
UCSC; uc002hvk.3; human.
CTD; 3859; -.
DisGeNET; 3859; -.
EuPathDB; HostDB:ENSG00000187242.4; -.
GeneCards; KRT12; -.
HGNC; HGNC:6414; KRT12.
HPA; HPA055217; -.
HPA; HPA055835; -.
MalaCards; KRT12; -.
MIM; 122100; phenotype.
MIM; 601687; gene.
neXtProt; NX_Q99456; -.
OpenTargets; ENSG00000187242; -.
Orphanet; 98954; Meesmann corneal dystrophy.
PharmGKB; PA30201; -.
eggNOG; ENOG410IFTF; Eukaryota.
eggNOG; ENOG410Y9IV; LUCA.
GeneTree; ENSGT00900000140820; -.
HOGENOM; HOG000230975; -.
HOVERGEN; HBG013015; -.
InParanoid; Q99456; -.
KO; K07604; -.
OMA; QNADHQR; -.
OrthoDB; EOG091G087I; -.
PhylomeDB; Q99456; -.
TreeFam; TF332742; -.
Reactome; R-HSA-6805567; Keratinization.
Reactome; R-HSA-6809371; Formation of the cornified envelope.
ChiTaRS; KRT12; human.
GeneWiki; Keratin_12; -.
GenomeRNAi; 3859; -.
PRO; PR:Q99456; -.
Proteomes; UP000005640; Chromosome 17.
Bgee; ENSG00000187242; -.
CleanEx; HS_KRT12; -.
Genevisible; Q99456; HS.
GO; GO:0005829; C:cytosol; TAS:Reactome.
GO; GO:0070062; C:extracellular exosome; HDA:UniProtKB.
GO; GO:0005882; C:intermediate filament; IEA:UniProtKB-KW.
GO; GO:0005198; F:structural molecule activity; NAS:ProtInc.
GO; GO:0070268; P:cornification; TAS:Reactome.
GO; GO:0031424; P:keratinization; TAS:Reactome.
GO; GO:0007601; P:visual perception; TAS:ProtInc.
InterPro; IPR001664; IF.
InterPro; IPR018039; IF_conserved.
InterPro; IPR039008; IF_rod_dom.
InterPro; IPR002957; Keratin_I.
PANTHER; PTHR23239; PTHR23239; 1.
Pfam; PF00038; Filament; 1.
PRINTS; PR01248; TYPE1KERATIN.
SMART; SM01391; Filament; 1.
PROSITE; PS00226; IF_ROD_1; 1.
PROSITE; PS51842; IF_ROD_2; 1.
1: Evidence at protein level;
Coiled coil; Complete proteome; Corneal dystrophy;
Direct protein sequencing; Disease mutation; Intermediate filament;
Keratin; Polymorphism; Reference proteome.
CHAIN 1 494 Keratin, type I cytoskeletal 12.
/FTId=PRO_0000063644.
DOMAIN 125 440 IF rod. {ECO:0000255|PROSITE-
ProRule:PRU01188}.
REGION 1 124 Head.
REGION 125 160 Coil 1A.
REGION 164 182 Linker 1.
REGION 183 274 Coil 1B.
REGION 275 297 Linker 12.
REGION 298 435 Coil 2.
REGION 436 494 Tail.
COMPBIAS 28 123 Gly-rich.
VARIANT 15 15 P -> S (in dbSNP:rs11650915).
{ECO:0000269|PubMed:18245975,
ECO:0000269|PubMed:20577595}.
/FTId=VAR_049783.
VARIANT 20 20 R -> W (in dbSNP:rs17566772).
{ECO:0000269|PubMed:10644419,
ECO:0000269|PubMed:18245975}.
/FTId=VAR_009547.
VARIANT 129 129 M -> T (in MECD; dbSNP:rs28936695).
{ECO:0000269|PubMed:10644419,
ECO:0000269|PubMed:16352477}.
/FTId=VAR_013126.
VARIANT 129 129 M -> V (in MECD; dbSNP:rs267607387).
{ECO:0000269|PubMed:20577595}.
/FTId=VAR_072069.
VARIANT 130 130 Q -> P (in MECD; dbSNP:rs58864803).
{ECO:0000269|PubMed:10781519}.
/FTId=VAR_013127.
VARIANT 132 132 L -> P (in MECD; dbSNP:rs886038212).
{ECO:0000269|PubMed:23222558}.
/FTId=VAR_072070.
VARIANT 135 135 R -> G (in MECD; dbSNP:rs58410481).
{ECO:0000269|PubMed:9399908}.
/FTId=VAR_008526.
VARIANT 135 135 R -> I (in MECD; dbSNP:rs57218384).
{ECO:0000269|PubMed:9399908}.
/FTId=VAR_008525.
VARIANT 135 135 R -> S (in MECD; dbSNP:rs61282718).
{ECO:0000269|PubMed:15148206}.
/FTId=VAR_031394.
VARIANT 135 135 R -> T (in MECD; dbSNP:rs57218384).
{ECO:0000269|PubMed:10644419,
ECO:0000269|PubMed:9171831}.
/FTId=VAR_003834.
VARIANT 137 137 A -> P (in MECD; dbSNP:rs58038639).
{ECO:0000269|PubMed:12543196}.
/FTId=VAR_031395.
VARIANT 140 140 L -> Q (in MECD).
{ECO:0000269|PubMed:24099278}.
/FTId=VAR_072071.
VARIANT 140 140 L -> R (in MECD; dbSNP:rs58918655).
{ECO:0000269|PubMed:9399908}.
/FTId=VAR_008527.
VARIANT 143 143 V -> L (in MECD; dbSNP:rs58343600).
{ECO:0000269|PubMed:18245975,
ECO:0000269|PubMed:9171831}.
/FTId=VAR_003835.
VARIANT 399 399 L -> LISNLEAQLL (in MECD).
/FTId=VAR_031396.
VARIANT 426 426 I -> S (in MECD; dbSNP:rs59350319).
{ECO:0000269|PubMed:16352477}.
/FTId=VAR_031397.
VARIANT 429 429 Y -> C (in MECD; dbSNP:rs59202432).
{ECO:0000269|PubMed:16227835}.
/FTId=VAR_031398.
VARIANT 429 429 Y -> D (in MECD; dbSNP:rs58162394).
{ECO:0000269|PubMed:9399908}.
/FTId=VAR_008528.
VARIANT 430 430 R -> P (in MECD; dbSNP:rs62635290).
{ECO:0000269|PubMed:17653038}.
/FTId=VAR_072072.
VARIANT 433 433 L -> R (in MECD; dbSNP:rs267607386).
{ECO:0000269|PubMed:18661274}.
/FTId=VAR_072073.
SEQUENCE 494 AA; 53511 MW; 75C981380532B682 CRC64;
MDLSNNTMSL SVRTPGLSRR LSSQSVIGRP RGMSASSVGS GYGGSAFGFG ASCGGGFSAA
SMFGSSSGFG GGSGSSMAGG LGAGYGRALG GGSFGGLGMG FGGSPGGGSL GILSGNDGGL
LSGSEKETMQ NLNDRLASYL DKVRALEEAN TELENKIREW YETRGTGTAD ASQSDYSKYY
PLIEDLRNKI ISASIGNAQL LLQIDNARLA AEDFRMKYEN ELALRQGVEA DINGLRRVLD
ELTLTRTDLE MQIESLNEEL AYMKKNHEDE LQSFRVGGPG EVSVEMDAAP GVDLTRLLND
MRAQYETIAE QNRKDAEAWF IEKSGELRKE ISTNTEQLQS SKSEVTDLRR AFQNLEIELQ
SQLAMKKSLE DSLAEAEGDY CAQLSQVQQL ISNLEAQLLQ VRADAERQNV DHQRLLNVKA
RLELEIETYR RLLDGEAQGD GLEESLFVTD SKSQAQSTDS SKDPTKTRKI KTVVQEMVNG
EVVSSQVQEI EELM


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E2288m ELISA kit 56 kDa cytokeratin,CK-10,Cytokeratin-10,K10,Keratin, type I cytoskeletal 10,Keratin, type I cytoskeletal 59 kDa,Keratin-10,Krt10,Krt1-10,Mouse,Mus musculus 96T
U1427m CLIA CK-2e,Cytokeratin-2e,Epithelial keratin-2e,K2e,K2e,Keratin, type II cytoskeletal 2 epidermal,Keratin-2 epidermis,Keratin-2e,Krt2,Krt2-17,Krt2a,Mouse,Mus musculus,Type-II keratin Kb2 96T
E1427m ELISA CK-2e,Cytokeratin-2e,Epithelial keratin-2e,K2e,K2e,Keratin, type II cytoskeletal 2 epidermal,Keratin-2 epidermis,Keratin-2e,Krt2,Krt2-17,Krt2a,Mouse,Mus musculus,Type-II keratin Kb2 96T
E1427m ELISA kit CK-2e,Cytokeratin-2e,Epithelial keratin-2e,K2e,K2e,Keratin, type II cytoskeletal 2 epidermal,Keratin-2 epidermis,Keratin-2e,Krt2,Krt2-17,Krt2a,Mouse,Mus musculus,Type-II keratin Kb2 96T
E2288m 56 kDa cytokeratin,CK-10,Cytokeratin-10,K10,Keratin, type I cytoskeletal 10,Keratin, type I cytoskeletal 59 kDa,Keratin-10,Krt10,Krt1-10,Mouse,Mus musculus
U1231m CLIA CK-18,Cytokeratin endo B,Cytokeratin-18,K18,Keratin D,Keratin, type I cytoskeletal 18,Keratin-18,Kerd,Krt1-18,Krt18,Mouse,Mus musculus 96T
E1231m ELISA kit CK-18,Cytokeratin endo B,Cytokeratin-18,K18,Keratin D,Keratin, type I cytoskeletal 18,Keratin-18,Kerd,Krt1-18,Krt18,Mouse,Mus musculus 96T
E1231m ELISA CK-18,Cytokeratin endo B,Cytokeratin-18,K18,Keratin D,Keratin, type I cytoskeletal 18,Keratin-18,Kerd,Krt1-18,Krt18,Mouse,Mus musculus 96T
E2282h ELISA kit 67 kDa cytokeratin,CK-1,Cytokeratin-1,Hair alpha protein,Homo sapiens,Human,K1,Keratin, type II cytoskeletal 1,Keratin-1,KRT1,KRTA,Type-II keratin Kb1 96T
E2282h ELISA 67 kDa cytokeratin,CK-1,Cytokeratin-1,Hair alpha protein,Homo sapiens,Human,K1,Keratin, type II cytoskeletal 1,Keratin-1,KRT1,KRTA,Type-II keratin Kb1 96T
U2282h CLIA kit 67 kDa cytokeratin,CK-1,Cytokeratin-1,Hair alpha protein,Homo sapiens,Human,K1,Keratin, type II cytoskeletal 1,Keratin-1,KRT1,KRTA,Type-II keratin Kb1 96T
U2282h CLIA 67 kDa cytokeratin,CK-1,Cytokeratin-1,Hair alpha protein,Homo sapiens,Human,K1,Keratin, type II cytoskeletal 1,Keratin-1,KRT1,KRTA,Type-II keratin Kb1 96T
E2282h 67 kDa cytokeratin,CK-1,Cytokeratin-1,Hair alpha protein,Homo sapiens,Human,K1,Keratin, type II cytoskeletal 1,Keratin-1,KRT1,KRTA,Type-II keratin Kb1
E2287m ELISA CK-8,Cytokeratin endo A,Cytokeratin-8,K8,Keratin, type II cytoskeletal 8,Keratin-8,Krt2-8,Krt8,Mouse,Mus musculus,Type-II keratin Kb8 96T
U2287r CLIA kit CK-8,Cytokeratin endo A,Cytokeratin-8,K8,Keratin, type II cytoskeletal 8,Keratin-8,Krt2-8,Krt8,Rat,Rattus norvegicus,Type-II keratin Kb8 96T
E2287r ELISA CK-8,Cytokeratin endo A,Cytokeratin-8,K8,Keratin, type II cytoskeletal 8,Keratin-8,Krt2-8,Krt8,Rat,Rattus norvegicus,Type-II keratin Kb8 96T


 

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