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

Aryl-hydrocarbon-interacting protein-like 1

 AIPL1_HUMAN             Reviewed;         384 AA.
Q9NZN9; D3DTM4; Q659W3; Q659W4; Q6ZZB6; Q8N6A0; Q9H873; Q9NS10;
11-JAN-2001, integrated into UniProtKB/Swiss-Prot.
19-SEP-2002, sequence version 2.
12-SEP-2018, entry version 168.
RecName: Full=Aryl-hydrocarbon-interacting protein-like 1;
Name=AIPL1; Synonyms=AIPL2;
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), NUCLEOTIDE SEQUENCE [GENOMIC
DNA] (ISOFORM 1), VARIANT HIS-90, AND VARIANT LCA4 ARG-239.
PubMed=10615133; DOI=10.1038/71732;
Sohocki M.M., Bowne S.J., Sullivan L.S., Blackshaw S., Cepko C.L.,
Payne A.M., Bhattacharya S.S., Khaliq S., Mehdi Q., Birch D.G.,
Harrison W.R., Elder F.F.B., Heckenlively J.R., Daiger S.P.;
"Mutations in a novel photoreceptor-pineal gene on 17p cause Leber
congenital amaurosis.";
Nat. Genet. 24:79-83(2000).
[2]
NUCLEOTIDE SEQUENCE [LARGE SCALE MRNA] (ISOFORM 3).
TISSUE=Retinoblastoma;
Guo J.H., Zhou G.J., Yu L.;
Submitted (JUL-2002) to the EMBL/GenBank/DDBJ databases.
[3]
NUCLEOTIDE SEQUENCE [LARGE SCALE MRNA] (ISOFORM 1).
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).
[4]
NUCLEOTIDE SEQUENCE [MRNA] (ISOFORMS 2; 4 AND 5).
TISSUE=Retina;
Janke B., Preising M., Lorenz B.;
"Alternative splicing in AIPL1: Implications on function and the
mutational spectrum.";
Submitted (MAR-2004) to the EMBL/GenBank/DDBJ databases.
[5]
NUCLEOTIDE SEQUENCE [MRNA] (ISOFORM 3).
TISSUE=Retinoblastoma;
Kato S.;
"Full-length cDNA derived from human retinoblastoma cell line Y79.";
Submitted (MAR-2011) to the EMBL/GenBank/DDBJ databases.
[6]
NUCLEOTIDE SEQUENCE [LARGE SCALE GENOMIC DNA].
PubMed=16625196; DOI=10.1038/nature04689;
Zody M.C., Garber M., Adams D.J., Sharpe T., Harrow J., Lupski J.R.,
Nicholson C., Searle S.M., Wilming L., Young S.K., Abouelleil A.,
Allen N.R., Bi W., Bloom T., Borowsky M.L., Bugalter B.E., Butler J.,
Chang J.L., Chen C.-K., Cook A., Corum B., Cuomo C.A., de Jong P.J.,
DeCaprio D., Dewar K., FitzGerald M., Gilbert J., Gibson R.,
Gnerre S., Goldstein S., Grafham D.V., Grocock R., Hafez N.,
Hagopian D.S., Hart E., Norman C.H., Humphray S., Jaffe D.B.,
Jones M., Kamal M., Khodiyar V.K., LaButti K., Laird G., Lehoczky J.,
Liu X., Lokyitsang T., Loveland J., Lui A., Macdonald P., Major J.E.,
Matthews L., Mauceli E., McCarroll S.A., Mihalev A.H., Mudge J.,
Nguyen C., Nicol R., O'Leary S.B., Osoegawa K., Schwartz D.C.,
Shaw-Smith C., Stankiewicz P., Steward C., Swarbreck D.,
Venkataraman V., Whittaker C.A., Yang X., Zimmer A.R., Bradley A.,
Hubbard T., Birren B.W., Rogers J., Lander E.S., Nusbaum C.;
"DNA sequence of human chromosome 17 and analysis of rearrangement in
the human lineage.";
Nature 440:1045-1049(2006).
[7]
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 (SEP-2005) to the EMBL/GenBank/DDBJ databases.
[8]
NUCLEOTIDE SEQUENCE [LARGE SCALE MRNA] (ISOFORM 1).
TISSUE=Eye;
PubMed=15489334; DOI=10.1101/gr.2596504;
The MGC Project Team;
"The status, quality, and expansion of the NIH full-length cDNA
project: the Mammalian Gene Collection (MGC).";
Genome Res. 14:2121-2127(2004).
[9]
INTERACTION WITH NUB1, SUBCELLULAR LOCATION, TISSUE SPECIFICITY,
MUTAGENESIS OF ARG-53; MET-79; VAL-96; ALA-197; ILE-206 AND GLY-262,
CHARACTERIZATION OF VARIANT LEU-302, AND CHARACTERIZATION OF VARIANT
LCA4 ARG-239.
TISSUE=Retina;
PubMed=12374762; DOI=10.1093/hmg/11.22.2723;
Akey D.T., Zhu X., Dyer M., Li A., Sorensen A., Blackshaw S.,
Fukuda-Kamitani T., Daiger S.P., Craft C.M., Kamitani T.,
Sohocki M.M.;
"The inherited blindness associated protein AIPL1 interacts with the
cell cycle regulator protein NUB1.";
Hum. Mol. Genet. 11:2723-2733(2002).
[10]
VARIANT LCA4 HIS-270, AND VARIANT LEU-302.
PubMed=17724218; DOI=10.1167/iovs.07-0068;
Simonelli F., Ziviello C., Testa F., Rossi S., Fazzi E., Bianchi P.E.,
Fossarello M., Signorini S., Bertone C., Galantuomo S., Brancati F.,
Valente E.M., Ciccodicola A., Rinaldi E., Auricchio A., Banfi S.;
"Clinical and molecular genetics of Leber's congenital amaurosis: a
multicenter study of Italian patients.";
Invest. Ophthalmol. Vis. Sci. 48:4284-4290(2007).
[11]
VARIANTS HIS-90 AND GLU-309 DELINS ASP-LEU-ASN-ARG-ARG-GLU-LEU.
PubMed=21602930; DOI=10.1371/journal.pone.0019458;
Li L., Xiao X., Li S., Jia X., Wang P., Guo X., Jiao X., Zhang Q.,
Hejtmancik J.F.;
"Detection of variants in 15 genes in 87 unrelated Chinese patients
with Leber congenital amaurosis.";
PLoS ONE 6:E19458-E19458(2011).
-!- FUNCTION: May be important in protein trafficking and/or protein
folding and stabilization.
-!- SUBUNIT: Interacts with NUB1. {ECO:0000269|PubMed:12374762}.
-!- INTERACTION:
Q9Y5A7:NUB1; NbExp=2; IntAct=EBI-6557414, EBI-3936907;
Q9BSI4:TINF2; NbExp=2; IntAct=EBI-6557414, EBI-717399;
-!- SUBCELLULAR LOCATION: Cytoplasm {ECO:0000269|PubMed:12374762}.
Nucleus {ECO:0000269|PubMed:12374762}.
-!- ALTERNATIVE PRODUCTS:
Event=Alternative splicing; Named isoforms=5;
Name=1;
IsoId=Q9NZN9-1; Sequence=Displayed;
Name=2;
IsoId=Q9NZN9-2; Sequence=VSP_041507;
Name=3; Synonyms=AIPL2;
IsoId=Q9NZN9-3; Sequence=VSP_041508;
Name=4;
IsoId=Q9NZN9-4; Sequence=VSP_047708;
Name=5;
IsoId=Q9NZN9-5; Sequence=VSP_047709;
-!- TISSUE SPECIFICITY: Highly expressed in retina. Specifically
localized to the developing photoreceptor layer and within the
photoreceptors of the adult retina. {ECO:0000269|PubMed:12374762}.
-!- DISEASE: Leber congenital amaurosis 4 (LCA4) [MIM:604393]: A
severe dystrophy of the retina, typically becoming evident in the
first years of life. Visual function is usually poor and often
accompanied by nystagmus, sluggish or near-absent pupillary
responses, photophobia, high hyperopia and keratoconus.
{ECO:0000269|PubMed:10615133, ECO:0000269|PubMed:12374762,
ECO:0000269|PubMed:17724218}. Note=The disease is caused by
mutations affecting the gene represented in this entry.
-!- WEB RESOURCE: Name=Mutations of the AIPL1 gene; Note=Retina
International's Scientific Newsletter;
URL="http://www.retina-international.org/files/sci-news/aipl1mut.htm";
-----------------------------------------------------------------------
Copyrighted by the UniProt Consortium, see https://www.uniprot.org/terms
Distributed under the Creative Commons Attribution (CC BY 4.0) License
-----------------------------------------------------------------------
EMBL; AF180472; AAF26708.1; -; Genomic_DNA.
EMBL; AF148864; AAF74023.1; -; mRNA.
EMBL; AF525970; AAM88405.1; -; mRNA.
EMBL; AK023970; BAB14744.1; -; mRNA.
EMBL; AJ633677; CAG17882.1; -; mRNA.
EMBL; AJ830742; CAH25995.1; -; mRNA.
EMBL; AJ830743; CAH25996.1; -; mRNA.
EMBL; AB593053; BAJ84000.1; -; mRNA.
EMBL; AB593054; BAJ84001.1; -; mRNA.
EMBL; AC055872; -; NOT_ANNOTATED_CDS; Genomic_DNA.
EMBL; CH471108; EAW90310.1; -; Genomic_DNA.
EMBL; CH471108; EAW90312.1; -; Genomic_DNA.
EMBL; CH471108; EAW90313.1; -; Genomic_DNA.
EMBL; CH471108; EAW90314.1; -; Genomic_DNA.
EMBL; BC012055; AAH12055.1; -; mRNA.
CCDS; CCDS11075.1; -. [Q9NZN9-1]
CCDS; CCDS32539.1; -. [Q9NZN9-2]
CCDS; CCDS32540.1; -. [Q9NZN9-3]
CCDS; CCDS67130.1; -. [Q9NZN9-4]
CCDS; CCDS67133.1; -. [Q9NZN9-5]
RefSeq; NP_001028226.1; NM_001033054.2. [Q9NZN9-3]
RefSeq; NP_001028227.1; NM_001033055.2. [Q9NZN9-2]
RefSeq; NP_001272328.1; NM_001285399.2.
RefSeq; NP_001272329.1; NM_001285400.2. [Q9NZN9-4]
RefSeq; NP_001272330.1; NM_001285401.2. [Q9NZN9-5]
RefSeq; NP_001272332.1; NM_001285403.2.
RefSeq; NP_055151.3; NM_014336.4. [Q9NZN9-1]
UniGene; Hs.279887; -.
PDB; 5U9A; X-ray; 2.70 A; A=2-161.
PDB; 5U9I; X-ray; 2.30 A; A=2-161.
PDB; 5U9J; X-ray; 2.10 A; A/B=2-161.
PDB; 5U9K; X-ray; 2.70 A; A=2-161.
PDB; 5V35; X-ray; 2.50 A; A=2-161.
PDBsum; 5U9A; -.
PDBsum; 5U9I; -.
PDBsum; 5U9J; -.
PDBsum; 5U9K; -.
PDBsum; 5V35; -.
ProteinModelPortal; Q9NZN9; -.
SMR; Q9NZN9; -.
BioGrid; 117248; 25.
IntAct; Q9NZN9; 20.
STRING; 9606.ENSP00000370521; -.
iPTMnet; Q9NZN9; -.
PhosphoSitePlus; Q9NZN9; -.
BioMuta; AIPL1; -.
DMDM; 23503042; -.
PaxDb; Q9NZN9; -.
PeptideAtlas; Q9NZN9; -.
PRIDE; Q9NZN9; -.
ProteomicsDB; 83467; -.
ProteomicsDB; 83468; -. [Q9NZN9-2]
ProteomicsDB; 83469; -. [Q9NZN9-3]
TopDownProteomics; Q9NZN9-1; -. [Q9NZN9-1]
TopDownProteomics; Q9NZN9-2; -. [Q9NZN9-2]
TopDownProteomics; Q9NZN9-3; -. [Q9NZN9-3]
DNASU; 23746; -.
Ensembl; ENST00000250087; ENSP00000250087; ENSG00000129221. [Q9NZN9-3]
Ensembl; ENST00000381129; ENSP00000370521; ENSG00000129221. [Q9NZN9-1]
Ensembl; ENST00000570466; ENSP00000461287; ENSG00000129221. [Q9NZN9-4]
Ensembl; ENST00000576307; ENSP00000459522; ENSG00000129221. [Q9NZN9-2]
Ensembl; ENST00000576776; ENSP00000460827; ENSG00000129221. [Q9NZN9-5]
GeneID; 23746; -.
KEGG; hsa:23746; -.
UCSC; uc002gcp.5; human. [Q9NZN9-1]
CTD; 23746; -.
DisGeNET; 23746; -.
EuPathDB; HostDB:ENSG00000129221.14; -.
GeneCards; AIPL1; -.
GeneReviews; AIPL1; -.
HGNC; HGNC:359; AIPL1.
HPA; HPA026578; -.
MalaCards; AIPL1; -.
MIM; 604392; gene.
MIM; 604393; phenotype.
neXtProt; NX_Q9NZN9; -.
OpenTargets; ENSG00000129221; -.
Orphanet; 1872; Cone rod dystrophy.
Orphanet; 65; Leber congenital amaurosis.
PharmGKB; PA24653; -.
eggNOG; KOG0545; Eukaryota.
eggNOG; ENOG410YGYV; LUCA.
GeneTree; ENSGT00390000001289; -.
HOGENOM; HOG000007366; -.
HOVERGEN; HBG004198; -.
InParanoid; Q9NZN9; -.
KO; K17767; -.
OMA; ETWNLSN; -.
OrthoDB; EOG091G0C69; -.
PhylomeDB; Q9NZN9; -.
TreeFam; TF314507; -.
GeneWiki; AIPL1; -.
GenomeRNAi; 23746; -.
PRO; PR:Q9NZN9; -.
Proteomes; UP000005640; Chromosome 17.
Bgee; ENSG00000129221; Expressed in 34 organ(s), highest expression level in pigmented layer of retina.
CleanEx; HS_AIPL1; -.
ExpressionAtlas; Q9NZN9; baseline and differential.
Genevisible; Q9NZN9; HS.
GO; GO:0005737; C:cytoplasm; IDA:MGI.
GO; GO:0005829; C:cytosol; IDA:HPA.
GO; GO:0005654; C:nucleoplasm; IDA:HPA.
GO; GO:0005634; C:nucleus; IDA:MGI.
GO; GO:0001917; C:photoreceptor inner segment; IEA:Ensembl.
GO; GO:0001918; F:farnesylated protein binding; IDA:MGI.
GO; GO:0051082; F:unfolded protein binding; TAS:ProtInc.
GO; GO:0043066; P:negative regulation of apoptotic process; IEA:Ensembl.
GO; GO:0007603; P:phototransduction, visible light; IEA:Ensembl.
GO; GO:0018343; P:protein farnesylation; IDA:MGI.
GO; GO:0022400; P:regulation of rhodopsin mediated signaling pathway; IEA:Ensembl.
GO; GO:0001895; P:retina homeostasis; IEA:Ensembl.
GO; GO:0007601; P:visual perception; TAS:ProtInc.
Gene3D; 1.25.40.10; -; 1.
InterPro; IPR031209; AIPL1.
InterPro; IPR001179; PPIase_FKBP_dom.
InterPro; IPR013026; TPR-contain_dom.
InterPro; IPR011990; TPR-like_helical_dom_sf.
InterPro; IPR019734; TPR_repeat.
PANTHER; PTHR11242:SF2; PTHR11242:SF2; 1.
Pfam; PF00254; FKBP_C; 1.
SMART; SM00028; TPR; 2.
SUPFAM; SSF48452; SSF48452; 1.
PROSITE; PS50293; TPR_REGION; 2.
1: Evidence at protein level;
3D-structure; Alternative splicing; Complete proteome; Cytoplasm;
Disease mutation; Leber congenital amaurosis; Nucleus; Polymorphism;
Reference proteome; Repeat; Sensory transduction; TPR repeat; Vision.
CHAIN 1 384 Aryl-hydrocarbon-interacting protein-like
1.
/FTId=PRO_0000075342.
DOMAIN 53 145 PPIase FKBP-type.
REPEAT 178 211 TPR 1.
REPEAT 230 263 TPR 2.
REPEAT 264 297 TPR 3.
VAR_SEQ 33 92 Missing (in isoform 2).
{ECO:0000303|Ref.4}.
/FTId=VSP_041507.
VAR_SEQ 33 54 Missing (in isoform 4).
{ECO:0000303|Ref.4}.
/FTId=VSP_047708.
VAR_SEQ 93 155 Missing (in isoform 3).
{ECO:0000303|Ref.2, ECO:0000303|Ref.5}.
/FTId=VSP_041508.
VAR_SEQ 215 238 Missing (in isoform 5).
{ECO:0000303|Ref.4}.
/FTId=VSP_047709.
VARIANT 33 33 V -> A (in dbSNP:rs16955859).
/FTId=VAR_050626.
VARIANT 90 90 D -> H (in dbSNP:rs12449580).
{ECO:0000269|PubMed:10615133,
ECO:0000269|PubMed:21602930}.
/FTId=VAR_010140.
VARIANT 134 134 Y -> F (in dbSNP:rs16955851).
/FTId=VAR_050627.
VARIANT 239 239 C -> R (in LCA4; no significant effect on
interaction with NUB1; dbSNP:rs62637012).
{ECO:0000269|PubMed:10615133,
ECO:0000269|PubMed:12374762}.
/FTId=VAR_010139.
VARIANT 270 270 R -> H (in LCA4).
{ECO:0000269|PubMed:17724218}.
/FTId=VAR_067165.
VARIANT 302 302 R -> L (found in a patient with LCA4;
there is no interaction with NUB1;
dbSNP:rs62637015).
{ECO:0000269|PubMed:12374762,
ECO:0000269|PubMed:17724218}.
/FTId=VAR_067166.
VARIANT 309 309 E -> DLNRREL (found in a patient with
LCA4). {ECO:0000269|PubMed:21602930}.
/FTId=VAR_067167.
MUTAGEN 53 53 R->W: No interaction with NUB1.
{ECO:0000269|PubMed:12374762}.
MUTAGEN 79 79 M->T: No interaction with NUB1.
{ECO:0000269|PubMed:12374762}.
MUTAGEN 96 96 V->I: No interaction with NUB1.
{ECO:0000269|PubMed:12374762}.
MUTAGEN 197 197 A->P: No significant effect on
interaction with NUB1.
{ECO:0000269|PubMed:12374762}.
MUTAGEN 206 206 I->N: No significant effect on
interaction with NUB1.
{ECO:0000269|PubMed:12374762}.
MUTAGEN 262 262 G->S: No interaction with NUB1.
{ECO:0000269|PubMed:12374762}.
CONFLICT 244 244 E -> K (in Ref. 3; CAG17882).
{ECO:0000305}.
CONFLICT 306 315 RLLENRMAEK -> EAAGEPHGGE (in Ref. 1;
AAF26708). {ECO:0000305}.
STRAND 12 18 {ECO:0000244|PDB:5U9J}.
STRAND 21 23 {ECO:0000244|PDB:5U9I}.
STRAND 32 40 {ECO:0000244|PDB:5U9J}.
STRAND 42 45 {ECO:0000244|PDB:5U9J}.
STRAND 48 51 {ECO:0000244|PDB:5U9J}.
HELIX 52 55 {ECO:0000244|PDB:5U9J}.
STRAND 59 62 {ECO:0000244|PDB:5U9J}.
STRAND 66 68 {ECO:0000244|PDB:5U9A}.
HELIX 71 76 {ECO:0000244|PDB:5U9J}.
STRAND 84 89 {ECO:0000244|PDB:5U9J}.
HELIX 91 94 {ECO:0000244|PDB:5U9J}.
HELIX 97 108 {ECO:0000244|PDB:5U9J}.
HELIX 116 129 {ECO:0000244|PDB:5U9J}.
HELIX 135 142 {ECO:0000244|PDB:5U9J}.
STRAND 147 157 {ECO:0000244|PDB:5U9J}.
SEQUENCE 384 AA; 43903 MW; 47F681A1DC91A82D CRC64;
MDAALLLNVE GVKKTILHGG TGELPNFITG SRVIFHFRTM KCDEERTVID DSRQVGQPMH
IIIGNMFKLE VWEILLTSMR VHEVAEFWCD TIHTGVYPIL SRSLRQMAQG KDPTEWHVHT
CGLANMFAYH TLGYEDLDEL QKEPQPLVFV IELLQVDAPS DYQRETWNLS NHEKMKAVPV
LHGEGNRLFK LGRYEEASSK YQEAIICLRN LQTKEKPWEV QWLKLEKMIN TLILNYCQCL
LKKEEYYEVL EHTSDILRHH PGIVKAYYVR ARAHAEVWNE AEAKADLQKV LELEPSMQKA
VRRELRLLEN RMAEKQEEER LRCRNMLSQG ATQPPAEPPT EPPAQSSTEP PAEPPTAPSA
ELSAGPPAEP ATEPPPSPGH SLQH


Related products :

Catalog number Product name Quantity
AIR AIP Gene aryl hydrocarbon receptor interacting protein
4853 (CT) Aryl hydrocarbon receptor interacting protein-like 1 0.5 mg
GWB-53FC53 AIP (aryl hydrocarbon receptor interacting protein)
GWB-59E120 AIP (aryl hydrocarbon receptor interacting protein)
E1428c Rat ELISA Kit FOR Aryl-hydrocarbon-interacting protein-like 1 96T
4853 (CT) Aryl hydrocarbon receptor interacting protein-like 1 0.1 mg
4865 (IN) Aryl hydrocarbon receptor interacting protein-like 1 0.1 mg
4865 (IN) Aryl hydrocarbon receptor interacting protein-like 1 0.5 mg
pro-886 Recombinant Human Aryl Hydrocarbon Receptor Interacting Protein AIP 1mg
pro-886 Recombinant Human Aryl Hydrocarbon Receptor Interacting Protein AIP 5
pro-886 Recombinant Human Aryl Hydrocarbon Receptor Interacting Protein 5
pro-886 Recombinant Human Aryl Hydrocarbon Receptor Interacting Protein 20
RPR-886 Recombinant Human Aryl Hydrocarbon Receptor Interacting Protein 5
E02A0543 Rat Aryl Hydrocarbon Receptor Interacting Protein ELISA , AIP
E02A0543 Rat Aryl Hydrocarbon Receptor Interacting Protein ELISA , AIP 96 Tests/kit
pro-886 Recombinant Human Aryl Hydrocarbon Receptor Interacting Protein AIP 20
E-EL-R0073 Rat AIP (Aryl Hydrocarbon Receptor Interacting Protein) ELISA Kit 96T
E02A0543 Rat Aryl Hydrocarbon Receptor Interacting Protein Elisa Kit (AIP) 96 Tests/kit
pro-886 Recombinant Human Aryl Hydrocarbon Receptor Interacting Protein 1mg
CSB-EL001501RA Rat Aryl-hydrocarbon-interacting protein-like 1(AIPL1) ELISA kit 96T
E02A0543 Rat Aryl Hydrocarbon Receptor Interacting Protein ELISA 96T/kit
E03A0543 Mouse Aryl Hydrocarbon Receptor Interacting Protein Elisa Kit (AIP) 96 Tests/kit
7-04297 Recombinant Human Aryl Hydrocarbon Receptor Interacting Protein 5
E06A0543 Goat Aryl Hydrocarbon Receptor Interacting Protein ELISA , AIP 96 Tests/kit
CSB-EL001501MO Mouse Aryl-hydrocarbon-interacting protein-like 1(AIPL1) ELISA kit 96T


 

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