SLC35F1 cDNA ORF clone, Homo sapiens(human)

Gene
Clones
gRNAs

Summary

Gene Symbol	SLC35F1
Entrez Gene ID	222553
Full Name	solute carrier family 35 member F1
Synonyms	C6orf169,dJ230I3.1
General protein information	Preferred Names solute carrier family 35 member F1 Names solute carrier family 35 member F1
Gene Type	protein-coding
Organism	Homo sapiens(human)
Genome	Chromosome: 6 Map Location: 6q22.2-q22.31

mRNA and Protein(s)

mRNA	Protein	Name
XM_005266865.3	XP_005266922.1	solute carrier family 35 member F1 isoform X1
XM_005266865.4	XP_005266922.1	solute carrier family 35 member F1 isoform X1
NM_001029858.3	NP_001025029.2	solute carrier family 35 member F1
NM_001029858.4	NP_001025029.2	solute carrier family 35 member F1

Pathways from BioSystems

Homologies

Gallus gallus (chicken)	SLC35F1	XP_001233614.1
Caenorhabditis elegans (roundworm)	Y73E7A.3	NP_001249010.1
Schizosaccharomyces pombe (fission yeast)	SPCC320.08	NP_587721.1
Xenopus tropicalis (tropical clawed frog)	slc35f1	XP_004914622.1
Oryza sativa (rice)	Os09g0513200	NP_001063649.2
Homo sapiens (human)	SLC35F1	NP_001025029.2
Pan troglodytes (chimpanzee)	SLC35F1	XP_527490.2
Mus musculus (house mouse)	Slc35f1	NP_848790.2
Danio rerio (zebrafish)	slc35f1	XP_005170256.1
	SLC35F1	XP_001110621.1
Canis lupus familiaris (dog)	SLC35F1	XP_541220.3
Bos taurus (cattle)	SLC35F1	XP_002690129.1
Arabidopsis thaliana (thale cress)	AT3G59320	NP_191491.2
Arabidopsis thaliana (thale cress)	AT3G59310	NP_191490.2
Oryza sativa (rice)	Os08g0540000	NP_001062380.1
Neurospora crassa	NCU00542	XP_963685.1
Rattus norvegicus (Norway rat)	Slc35f1	NP_001102808.1
Magnaporthe oryzae (rice blast fungus)	MGG_03107	XP_003720565.1
Arabidopsis thaliana (thale cress)	AT3G59340	NP_567081.1
Oryza sativa (rice)	Os05g0299500	NP_001055130.2

Gene Ontology
Bibliography

Related articles in PubMed

Genetic association study of QT interval highlights role for calcium signaling pathways in myocardial repolarization.
Arking DE, Pulit SL, Crotti L, van der Harst P, Munroe PB, Koopmann TT, Sotoodehnia N, Rossin EJ, Morley M, Wang X, Johnson AD, Lundby A, Gudbjartsson DF, Noseworthy PA, Eijgelsheim M, Bradford Y, Tarasov KV, D?rr M, M?ller-Nurasyid M, Lahtinen AM, Nolte IM, Smith AV, Bis JC, Isaacs A, Newhouse SJ, Evans DS, Post WS, Waggott D, Lyytik?inen LP, Hicks AA, Eisele L, Ellinghaus D, Hayward C, Navarro P, Ulivi S, Tanaka T, Tester DJ, Chatel S, Gustafsson S, Kumari M, Morris RW, Naluai ?T, Padmanabhan S, Kluttig A, Strohmer B, Panayiotou AG, Torres M, Knoflach M, Hubacek JA, Slowikowski K, Raychaudhuri S, Kumar RD, Harris TB, Launer LJ, Shuldiner AR, Alonso A, Bader JS, Ehret G, Huang H, Kao WH, Strait JB, Macfarlane PW, Brown M, Caulfield MJ, Samani NJ, Kronenberg F, Willeit J, , , Smith JG, Greiser KH, Meyer Zu Schwabedissen H, Werdan K, Carella M, Zelante L, Heckbert SR, Psaty BM, Rotter JI, Kolcic I, Pola?ek O, Wright AF, Griffin M, Daly MJ, , Arnar DO, H?lm H, Thorsteinsdottir U, , Denny JC, Roden DM, Zuvich RL, Emilsson V, Plump AS, Larson MG, O'Donnell CJ, Yin X, Bobbo M, D'Adamo AP, Iorio A, Sinagra G, Carracedo A, Cummings SR, Nalls MA, Jula A, Kontula KK, Marjamaa A, Oikarinen L, Perola M, Porthan K, Erbel R, Hoffmann P, J?ckel KH, K?lsch H, N?then MM, , den Hoed M, Loos RJ, Thelle DS, Gieger C, Meitinger T, Perz S, Peters A, Prucha H, Sinner MF, Waldenberger M, de Boer RA, Franke L, van der Vleuten PA, Beckmann BM, Martens E, Bardai A, Hofman N, Wilde AA, Behr ER, Dalageorgou C, Giudicessi JR, Medeiros-Domingo A, Barc J, Kyndt F, Probst V, Ghidoni A, Insolia R, Hamilton RM, Scherer SW, Brandimarto J, Margulies K, Moravec CE, del Greco M F, Fuchsberger C, O'Connell JR, Lee WK, Watt GC, Campbell H, Wild SH, El Mokhtari NE, Frey N, Asselbergs FW, Mateo Leach I, Navis G, van den Berg MP, van Veldhuisen DJ, Kellis M, Krijthe BP, Franco OH, Hofman A, Kors JA, Uitterlinden AG, Witteman JC, Kedenko L, Lamina C, Oostra BA, Abecasis GR, Lakatta EG, Mulas A, Orr? M, Schlessinger D, Uda M, Markus MR, V?lker U, Snieder H, Spector TD, ?rnl?v J, Lind L, Sundstr?m J, Syv?nen AC, Kivimaki M, K?h?nen M, Mononen N, Raitakari OT, Viikari JS, Adamkova V, Kiechl S, Brion M, Nicolaides AN, Paulweber B, Haerting J, Dominiczak AF, Nyberg F, Whincup PH, Hingorani AD, Schott JJ, Bezzina CR, Ingelsson E, Ferrucci L, Gasparini P, Wilson JF, Rudan I, Franke A, M?hleisen TW, Pramstaller PP, Lehtim?ki TJ, Paterson AD, Parsa A, Liu Y, van Duijn CM, Siscovick DS, Gudnason V, Jamshidi Y, Salomaa V, Felix SB, Sanna S, Ritchie MD, Stricker BH, Stefansson K, Boyer LA, Cappola TP, Olsen JV, Lage K, Schwartz PJ, K??b S, Chakravarti A, Ackerman MJ, Pfeufer A, de Bakker PI, Newton-Cheh C
Nature genetics46(8)826-36(2014 Aug)

Genome-wide association analyses suggest NELL1 influences adverse metabolic response to HCTZ in African Americans.
Del-Aguila JL, Beitelshees AL, Cooper-Dehoff RM, Chapman AB, Gums JG, Bailey K, Gong Y, Turner ST, Johnson JA, Boerwinkle E
The pharmacogenomics journal14(1)35-40(2014 Feb)

Identification of heart rate-associated loci and their effects on cardiac conduction and rhythm disorders.
den Hoed M, Eijgelsheim M, Esko T, Brundel BJ, Peal DS, Evans DM, Nolte IM, Segr? AV, Holm H, Handsaker RE, Westra HJ, Johnson T, Isaacs A, Yang J, Lundby A, Zhao JH, Kim YJ, Go MJ, Almgren P, Bochud M, Boucher G, Cornelis MC, Gudbjartsson D, Hadley D, van der Harst P, Hayward C, den Heijer M, Igl W, Jackson AU, Kutalik Z, Luan J, Kemp JP, Kristiansson K, Ladenvall C, Lorentzon M, Montasser ME, Njajou OT, O'Reilly PF, Padmanabhan S, St Pourcain B, Rankinen T, Salo P, Tanaka T, Timpson NJ, Vitart V, Waite L, Wheeler W, Zhang W, Draisma HH, Feitosa MF, Kerr KF, Lind PA, Mihailov E, Onland-Moret NC, Song C, Weedon MN, Xie W, Yengo L, Absher D, Albert CM, Alonso A, Arking DE, de Bakker PI, Balkau B, Barlassina C, Benaglio P, Bis JC, Bouatia-Naji N, Brage S, Chanock SJ, Chines PS, Chung M, Darbar D, Dina C, D?rr M, Elliott P, Felix SB, Fischer K, Fuchsberger C, de Geus EJ, Goyette P, Gudnason V, Harris TB, Hartikainen AL, Havulinna AS, Heckbert SR, Hicks AA, Hofman A, Holewijn S, Hoogstra-Berends F, Hottenga JJ, Jensen MK, Johansson A, Junttila J, K??b S, Kanon B, Ketkar S, Khaw KT, Knowles JW, Kooner AS, Kors JA, Kumari M, Milani L, Laiho P, Lakatta EG, Langenberg C, Leusink M, Liu Y, Luben RN, Lunetta KL, Lynch SN, Markus MR, Marques-Vidal P, Mateo Leach I, McArdle WL, McCarroll SA, Medland SE, Miller KA, Montgomery GW, Morrison AC, M?ller-Nurasyid M, Navarro P, Nelis M, O'Connell JR, O'Donnell CJ, Ong KK, Newman AB, Peters A, Polasek O, Pouta A, Pramstaller PP, Psaty BM, Rao DC, Ring SM, Rossin EJ, Rudan D, Sanna S, Scott RA, Sehmi JS, Sharp S, Shin JT, Singleton AB, Smith AV, Soranzo N, Spector TD, Stewart C, Stringham HM, Tarasov KV, Uitterlinden AG, Vandenput L, Hwang SJ, Whitfield JB, Wijmenga C, Wild SH, Willemsen G, Wilson JF, Witteman JC, Wong A, Wong Q, Jamshidi Y, Zitting P, Boer JM, Boomsma DI, Borecki IB, van Duijn CM, Ekelund U, Forouhi NG, Froguel P, Hingorani A, Ingelsson E, Kivimaki M, Kronmal RA, Kuh D, Lind L, Martin NG, Oostra BA, Pedersen NL, Quertermous T, Rotter JI, van der Schouw YT, Verschuren WM, Walker M, Albanes D, Arnar DO, Assimes TL, Bandinelli S, Boehnke M, de Boer RA, Bouchard C, Caulfield WL, Chambers JC, Curhan G, Cusi D, Eriksson J, Ferrucci L, van Gilst WH, Glorioso N, de Graaf J, Groop L, Gyllensten U, Hsueh WC, Hu FB, Huikuri HV, Hunter DJ, Iribarren C, Isomaa B, Jarvelin MR, Jula A, K?h?nen M, Kiemeney LA, van der Klauw MM, Kooner JS, Kraft P, Iacoviello L, Lehtim?ki T, Lokki ML, Mitchell BD, Navis G, Nieminen MS, Ohlsson C, Poulter NR, Qi L, Raitakari OT, Rimm EB, Rioux JD, Rizzi F, Rudan I, Salomaa V, Sever PS, Shields DC, Shuldiner AR, Sinisalo J, Stanton AV, Stolk RP, Strachan DP, Tardif JC, Thorsteinsdottir U, Tuomilehto J, van Veldhuisen DJ, Virtamo J, Viikari J, Vollenweider P, Waeber G, Widen E, Cho YS, Olsen JV, Visscher PM, Willer C, Franke L, , , Erdmann J, Thompson JR, , Pfeufer A, , Sotoodehnia N, , Newton-Cheh C, , Ellinor PT, Stricker BH, Metspalu A, Perola M, Beckmann JS, Smith GD, Stefansson K, Wareham NJ, Munroe PB, Sibon OC, Milan DJ, Snieder H, Samani NJ, Loos RJ
Nature genetics45(6)621-31(2013 Jun)

Genome-wide association analysis identifies multiple loci related to resting heart rate.
Eijgelsheim M, Newton-Cheh C, Sotoodehnia N, de Bakker PI, M?ller M, Morrison AC, Smith AV, Isaacs A, Sanna S, D?rr M, Navarro P, Fuchsberger C, Nolte IM, de Geus EJ, Estrada K, Hwang SJ, Bis JC, R?ckert IM, Alonso A, Launer LJ, Hottenga JJ, Rivadeneira F, Noseworthy PA, Rice KM, Perz S, Arking DE, Spector TD, Kors JA, Aulchenko YS, Tarasov KV, Homuth G, Wild SH, Marroni F, Gieger C, Licht CM, Prineas RJ, Hofman A, Rotter JI, Hicks AA, Ernst F, Najjar SS, Wright AF, Peters A, Fox ER, Oostra BA, Kroemer HK, Couper D, V?lzke H, Campbell H, Meitinger T, Uda M, Witteman JC, Psaty BM, Wichmann HE, Harris TB, K??b S, Siscovick DS, Jamshidi Y, Uitterlinden AG, Folsom AR, Larson MG, Wilson JF, Penninx BW, Snieder H, Pramstaller PP, van Duijn CM, Lakatta EG, Felix SB, Gudnason V, Pfeufer A, Heckbert SR, Stricker BH, Boerwinkle E, O'Donnell CJ
Human molecular genetics19(19)3885-94(2010 Oct)

Genome-wide pleiotropy of osteoporosis-related phenotypes: the Framingham Study.
Karasik D, Hsu YH, Zhou Y, Cupples LA, Kiel DP, Demissie S
Journal of bone and mineral research : the official journal of the American Society for Bone and Mineral Research25(7)1555-63(2010 Jul)

GeneRIFs: Gene References Into Functions What's a GeneRIF?

Observational study, meta-analysis, and genome-wide association study of gene-disease association. (HuGE Navigator)
Title: Genome-wide association analysis identifies multiple loci related to resting heart rate.

Observational study and genome-wide association study of gene-disease association. (HuGE Navigator)
Title: Genome-wide pleiotropy of osteoporosis-related phenotypes: the Framingham Study.

Clinical trial of gene-disease association and gene-environment interaction. (HuGE Navigator)
Title: Personalized smoking cessation: interactions between nicotine dose, dependence and quit-success genotype score.

Meta-analysis and genome-wide association study of gene-disease association. (HuGE Navigator)
Title: Genetic variants associated with cardiac structure and function: a meta-analysis and replication of genome-wide association data.

The following SLC35F1 gene cDNA ORF clone sequences were retrieved from the NCBI Reference Sequence Database (RefSeq). These sequences represent the protein coding region of the SLC35F1 cDNA ORF which is encoded by the open reading frame (ORF) sequence. ORF sequences can be delivered in our standard vector, pcDNA3.1⁺/C-(K)DYK or the vector of your choice as an expression/transfection-ready ORF clone. Not the clone you want? Click here to find your clone.

***CloneID	Accession No.	Definition	**Vector	*Turnaround time	Price (USD)
OHu24322	NM_001029858.4 Latest version!	Homo sapiens solute carrier family 35 member F1 (SLC35F1), mRNA.	pcDNA3.1-C-(k)DYK or customized vector	in pcDNA3.1-C-(k)DYK	$159.50-$223.30 $319.00
OHu24322	XM_005266865.4 Latest version!	Homo sapiens solute carrier family 35 member F1 (SLC35F1), transcript variant X1, mRNA.	pcDNA3.1-C-(k)DYK or customized vector	in pcDNA3.1-C-(k)DYK	$159.50-$223.30 $319.00
View Old Accession Versions >>
OHu24322	XM_005266865.3	Homo sapiens solute carrier family 35, member F1 (SLC35F1), transcript variant X1, mRNA.	pcDNA3.1-C-(k)DYK or customized vector	in pcDNA3.1-C-(k)DYK	$159.50-$223.30 $319.00
OHu24322	NM_001029858.3	Homo sapiens solute carrier family 35 member F1 (SLC35F1), mRNA.	pcDNA3.1-C-(k)DYK or customized vector	in pcDNA3.1-C-(k)DYK	$159.50-$223.30 $319.00
Hide Old Accession Versions >>

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** GenScript guarantees 100% sequence accuracy of all synthetic DNA constructs we deliver, but we do not guarantee protein expression in your experimental system. Protein expression is influenced by many factors that may vary between experiments or laboratories. In addition, please pay attention to the signal peptide, propeptide and transit peptide in target ORF, which may affect the choice of vector (N/C terminal tag vector).

***One clone ID might be correlated to multiple accession numbers, which share the same CDS sequence.

Reference Sequences (Refseq)

SLC35F1 ( NM_001029858.3 ) cDNA ORF clone, Homo sapiens(human) -> NP_001025029.2 Homo sapiens solute carrier family 35 member F1 (SLC35F1), mRNA.

Price & Availability↑

CloneID	OHu24322
Clone ID Related Accession (Same CDS sequence)	XM_005266865.3 , XM_005266865.4 , NM_001029858.3 , NM_001029858.4
Accession Version	NM_001029858.3	Documents for ORF clone product in default vector
Sequence Information	ORF Nucleotide Sequence (Length: 1227bp) Protein sequence SNP
Vector	pcDNA3.1-C-(k)DYK or customized vector	User Manual
Clone information	Clone Map	MSDS
Tag on pcDNA3.1⁺/C-(K)DYK	C terminal DYKDDDDK tags
ORF Insert Method	CloneEZ™ Seamless cloning technology
Insert Structure	linear
Update Date	2017-10-01
Organism	Homo sapiens(human)
Product	solute carrier family 35 member F1
Comment	Comment: VALIDATED REFSEQ: This record has undergone validation or preliminary review. The reference sequence was derived from AL136478.9, Z95326.1, AL449196.1 and AL133379.3. On May 23, 2008 this sequence version replaced NM_001029858.2. Sequence Note: The RefSeq transcript and protein were derived from genomic sequence to make the sequence consistent with the reference genome assembly. The genomic coordinates used for the transcript record were based on alignments. ##Evidence-Data-START## Transcript exon combination :: BC028615.1, SRR1803612.90006.1 [ECO:0000332] RNAseq introns :: single sample supports all introns SAMEA2145240, SAMEA2145313 [ECO:0000348] ##Evidence-Data-END##

ATGATCCCCC CTGAGCAGCC GCAGCAGCAG CTGCAGCCGC CGTCGCCAGC CCCGCCGAAC 
CATGTGGTGA CCACCATCGA GAACCTGCCG GCCGAGGGCA GCGGCGGCGG CGGGAGCCTG 
TCCGCCTCCT CCCGGGCTGG CGTGCGCCAG AGGATCCGCA AAGTGCTGAA CAGGGAGATG 
TTAATCTCTG TGGCCCTAGG CCAGGTGTTA TCCCTCCTTA TTTGTGGAAT TGGCTTGACT 
AGCAAGTATC TGTCAGAAGA TTTCCACGCC AACACACCAG TCTTCCAGAG TTTCCTCAAT 
TACATTCTTC TCTTCTTGGT CTATACCACC ACACTAGCCG TCAGACAAGG AGAAGAAAAC 
CTCCTGGCAA TTTTACGACG AAGATGGTGG AAGTACATGA TTTTGGGACT CATAGACCTG 
GAAGCAAATT ATCTGGTGGT CAAGGCTTAC CAATACACAA CTCTGACCAG TATCCAGCTC 
CTGGACTGTT TTGTGATCCC AGTCGTGATT TTGCTCTCCT GGTTCTTCCT GCTGATCCGG 
TACAAGGCTG TGCATTTCAT CGGCATCGTT GTCTGCATCC TGGGAATGGG CTGCATGGTG 
GGAGCAGATG TGCTTGTGGG AAGACATCAG GGAGCAGGGG AAAATAAGCT GGTAGGGGAC 
CTTCTGGTCT TAGGAGGAGC CACACTCTAT GGTATTTCTA ACGTCTGGGA AGAATACATC 
ATCCGAACTC TGAGCCGAGT GGAATTCCTG GGAATGATTG GTCTCTTTGG AGCATTTTTC 
AGTGGAATTC AATTAGCTAT AATGGAGCAT AAGGAACTGT TGAAGGTGCC CTGGGACTGG 
CAAATAGGAC TGCTCTACGT TGGCTTTAGT GCCTGCATGT TTGGTCTCTA CAGCTTTATG 
CCAGTCGTCA TAAAGAAAAC CAGTGCCACT TCAGTCAACC TCTCCTTGCT CACAGCAGAC 
TTGTACAGCC TGTTCTGTGG ATTGTTTCTC TTCCACTACA AGTTTTCAGG ACTTTATCTC 
CTGTCTTTCT TCACCATCCT CATTGGGCTG GTGCTCTACT CCTCCACCTC CACCTACATA 
GCCCAGGACC CCCGAGTGTA TAAGCAGTTC CGCAATCCTT CAGGACCTGT TGTGGACTTA 
CCGACCACAG CTCAGGTGGA ACCCTCAGTC ACCTACACCA GCCTGGGCCA GGAGACCGAA 
GAGGAGCCTC ATGTTCGTGT GGCCTAG

The stop codons will be deleted if pcDNA3.1⁺/C-(K)DYK vector is selected.

RefSeq	NP_001025029.2
CDS	202..1428
Translation	MIPPEQPQQQLQPPSPAPPNHVVTTIENLPAEGSGGGGSLSASSRAGVRQRIRKVLNREMLISVALGQVLSLLICGIGLTSKYLSEDFHANTPVFQSFLNYILLFLVYTTTLAVRQGEENLLAILRRRWWKYMILGLIDLEANYLVVKAYQYTTLTSIQLLDCFVIPVVILLSWFFLLIRYKAVHFIGIVVCILGMGCMVGADVLVGRHQGAGENKLVGDLLVLGGATLYGISNVWEEYIIRTLSRVEFLGMIGLFGAFFSGIQLAIMEHKELLKVPWDWQIGLLYVGFSACMFGLYSFMPVVIKKTSATSVNLSLLTADLYSLFCGLFLFHYKFSGLYLLSFFTILIGLVLYSSTSTYIAQDPRVYKQFRNPSGPVVDLPTTAQVEPSVTYTSLGQETEEEPHVRVA

Target ORF information:

RefSeq Version	NM_001029858.3
Organism	Homo sapiens(human)
Definition	Homo sapiens solute carrier family 35 member F1 (SLC35F1), mRNA.

Target ORF information:

Epitope	DYKDDDDK
Bacterial selection	AMP^R
Mammalian selection	Neo^R
Vector	pcDNA3.1⁺/C-(K)DYK

NM_001029858.3

ORF Insert Sequence:

ATGATCCCCC CTGAGCAGCC GCAGCAGCAG CTGCAGCCGC CGTCGCCAGC CCCGCCGAAC 
CATGTGGTGA CCACCATCGA GAACCTGCCG GCCGAGGGCA GCGGCGGCGG CGGGAGCCTG 
TCCGCCTCCT CCCGGGCTGG CGTGCGCCAG AGGATCCGCA AAGTGCTGAA CAGGGAGATG 
TTAATCTCTG TGGCCCTAGG CCAGGTGTTA TCCCTCCTTA TTTGTGGAAT TGGCTTGACT 
AGCAAGTATC TGTCAGAAGA TTTCCACGCC AACACACCAG TCTTCCAGAG TTTCCTCAAT 
TACATTCTTC TCTTCTTGGT CTATACCACC ACACTAGCCG TCAGACAAGG AGAAGAAAAC 
CTCCTGGCAA TTTTACGACG AAGATGGTGG AAGTACATGA TTTTGGGACT CATAGACCTG 
GAAGCAAATT ATCTGGTGGT CAAGGCTTAC CAATACACAA CTCTGACCAG TATCCAGCTC 
CTGGACTGTT TTGTGATCCC AGTCGTGATT TTGCTCTCCT GGTTCTTCCT GCTGATCCGG 
TACAAGGCTG TGCATTTCAT CGGCATCGTT GTCTGCATCC TGGGAATGGG CTGCATGGTG 
GGAGCAGATG TGCTTGTGGG AAGACATCAG GGAGCAGGGG AAAATAAGCT GGTAGGGGAC 
CTTCTGGTCT TAGGAGGAGC CACACTCTAT GGTATTTCTA ACGTCTGGGA AGAATACATC 
ATCCGAACTC TGAGCCGAGT GGAATTCCTG GGAATGATTG GTCTCTTTGG AGCATTTTTC 
AGTGGAATTC AATTAGCTAT AATGGAGCAT AAGGAACTGT TGAAGGTGCC CTGGGACTGG 
CAAATAGGAC TGCTCTACGT TGGCTTTAGT GCCTGCATGT TTGGTCTCTA CAGCTTTATG 
CCAGTCGTCA TAAAGAAAAC CAGTGCCACT TCAGTCAACC TCTCCTTGCT CACAGCAGAC 
TTGTACAGCC TGTTCTGTGG ATTGTTTCTC TTCCACTACA AGTTTTCAGG ACTTTATCTC 
CTGTCTTTCT TCACCATCCT CATTGGGCTG GTGCTCTACT CCTCCACCTC CACCTACATA 
GCCCAGGACC CCCGAGTGTA TAAGCAGTTC CGCAATCCTT CAGGACCTGT TGTGGACTTA 
CCGACCACAG CTCAGGTGGA ACCCTCAGTC ACCTACACCA GCCTGGGCCA GGAGACCGAA 
GAGGAGCCTC ATGTTCGTGT GGCCTAG

The stop codons will be deleted if pcDNA3.1⁺/C-(K)DYK vector is selected.

SLC35F1 ( NM_001029858.4 ) cDNA ORF clone, Homo sapiens(human) -> NP_001025029.2 Homo sapiens solute carrier family 35 member F1 (SLC35F1), mRNA.

Price & Availability↑

CloneID	OHu24322
Clone ID Related Accession (Same CDS sequence)	XM_005266865.3 , XM_005266865.4 , NM_001029858.3 , NM_001029858.4
Accession Version	NM_001029858.4 Latest version!	Documents for ORF clone product in default vector
Sequence Information	ORF Nucleotide Sequence (Length: 1227bp) Protein sequence SNP
Vector	pcDNA3.1-C-(k)DYK or customized vector	User Manual
Clone information	Clone Map	MSDS
Tag on pcDNA3.1⁺/C-(K)DYK	C terminal DYKDDDDK tags
ORF Insert Method	CloneEZ™ Seamless cloning technology
Insert Structure	linear
Update Date	2019-04-30
Organism	Homo sapiens(human)
Product	solute carrier family 35 member F1
Comment	Comment: VALIDATED REFSEQ: This record has undergone validation or preliminary review. The reference sequence was derived from AL136478.9, Z95326.1, AL449196.1 and AL133379.3. On Nov 22, 2018 this sequence version replaced NM_001029858.3. Sequence Note: The RefSeq transcript and protein were derived from genomic sequence to make the sequence consistent with the reference genome assembly. The genomic coordinates used for the transcript record were based on alignments. ##Evidence-Data-START## Transcript exon combination :: BC028615.1, SRR1803612.90006.1 [ECO:0000332] RNAseq introns :: single sample supports all introns SAMEA2145240, SAMEA2145313 [ECO:0000348] ##Evidence-Data-END## ##RefSeq-Attributes-START## MANE Ensembl match :: ENST00000360388.9/ ENSP00000353557.4 RefSeq Select criteria :: based on conservation, expression, longest protein ##RefSeq-Attributes-END## COMPLETENESS: full length.

ATGATCCCCC CTGAGCAGCC GCAGCAGCAG CTGCAGCCGC CGTCGCCAGC CCCGCCGAAC 
CATGTGGTGA CCACCATCGA GAACCTGCCG GCCGAGGGCA GCGGCGGCGG CGGGAGCCTG 
TCCGCCTCCT CCCGGGCTGG CGTGCGCCAG AGGATCCGCA AAGTGCTGAA CAGGGAGATG 
TTAATCTCTG TGGCCCTAGG CCAGGTGTTA TCCCTCCTTA TTTGTGGAAT TGGCTTGACT 
AGCAAGTATC TGTCAGAAGA TTTCCACGCC AACACACCAG TCTTCCAGAG TTTCCTCAAT 
TACATTCTTC TCTTCTTGGT CTATACCACC ACACTAGCCG TCAGACAAGG AGAAGAAAAC 
CTCCTGGCAA TTTTACGACG AAGATGGTGG AAGTACATGA TTTTGGGACT CATAGACCTG 
GAAGCAAATT ATCTGGTGGT CAAGGCTTAC CAATACACAA CTCTGACCAG TATCCAGCTC 
CTGGACTGTT TTGTGATCCC AGTCGTGATT TTGCTCTCCT GGTTCTTCCT GCTGATCCGG 
TACAAGGCTG TGCATTTCAT CGGCATCGTT GTCTGCATCC TGGGAATGGG CTGCATGGTG 
GGAGCAGATG TGCTTGTGGG AAGACATCAG GGAGCAGGGG AAAATAAGCT GGTAGGGGAC 
CTTCTGGTCT TAGGAGGAGC CACACTCTAT GGTATTTCTA ACGTCTGGGA AGAATACATC 
ATCCGAACTC TGAGCCGAGT GGAATTCCTG GGAATGATTG GTCTCTTTGG AGCATTTTTC 
AGTGGAATTC AATTAGCTAT AATGGAGCAT AAGGAACTGT TGAAGGTGCC CTGGGACTGG 
CAAATAGGAC TGCTCTACGT TGGCTTTAGT GCCTGCATGT TTGGTCTCTA CAGCTTTATG 
CCAGTCGTCA TAAAGAAAAC CAGTGCCACT TCAGTCAACC TCTCCTTGCT CACAGCAGAC 
TTGTACAGCC TGTTCTGTGG ATTGTTTCTC TTCCACTACA AGTTTTCAGG ACTTTATCTC 
CTGTCTTTCT TCACCATCCT CATTGGGCTG GTGCTCTACT CCTCCACCTC CACCTACATA 
GCCCAGGACC CCCGAGTGTA TAAGCAGTTC CGCAATCCTT CAGGACCTGT TGTGGACTTA 
CCGACCACAG CTCAGGTGGA ACCCTCAGTC ACCTACACCA GCCTGGGCCA GGAGACCGAA 
GAGGAGCCTC ATGTTCGTGT GGCCTAG

The stop codons will be deleted if pcDNA3.1⁺/C-(K)DYK vector is selected.

RefSeq	NP_001025029.2
CDS	464..1690
Translation	MIPPEQPQQQLQPPSPAPPNHVVTTIENLPAEGSGGGGSLSASSRAGVRQRIRKVLNREMLISVALGQVLSLLICGIGLTSKYLSEDFHANTPVFQSFLNYILLFLVYTTTLAVRQGEENLLAILRRRWWKYMILGLIDLEANYLVVKAYQYTTLTSIQLLDCFVIPVVILLSWFFLLIRYKAVHFIGIVVCILGMGCMVGADVLVGRHQGAGENKLVGDLLVLGGATLYGISNVWEEYIIRTLSRVEFLGMIGLFGAFFSGIQLAIMEHKELLKVPWDWQIGLLYVGFSACMFGLYSFMPVVIKKTSATSVNLSLLTADLYSLFCGLFLFHYKFSGLYLLSFFTILIGLVLYSSTSTYIAQDPRVYKQFRNPSGPVVDLPTTAQVEPSVTYTSLGQETEEEPHVRVA

Target ORF information:

RefSeq Version	NM_001029858.4
Organism	Homo sapiens(human)
Definition	Homo sapiens solute carrier family 35 member F1 (SLC35F1), mRNA.

Target ORF information:

Epitope	DYKDDDDK
Bacterial selection	AMP^R
Mammalian selection	Neo^R
Vector	pcDNA3.1⁺/C-(K)DYK

NM_001029858.4

ORF Insert Sequence:

ATGATCCCCC CTGAGCAGCC GCAGCAGCAG CTGCAGCCGC CGTCGCCAGC CCCGCCGAAC 
CATGTGGTGA CCACCATCGA GAACCTGCCG GCCGAGGGCA GCGGCGGCGG CGGGAGCCTG 
TCCGCCTCCT CCCGGGCTGG CGTGCGCCAG AGGATCCGCA AAGTGCTGAA CAGGGAGATG 
TTAATCTCTG TGGCCCTAGG CCAGGTGTTA TCCCTCCTTA TTTGTGGAAT TGGCTTGACT 
AGCAAGTATC TGTCAGAAGA TTTCCACGCC AACACACCAG TCTTCCAGAG TTTCCTCAAT 
TACATTCTTC TCTTCTTGGT CTATACCACC ACACTAGCCG TCAGACAAGG AGAAGAAAAC 
CTCCTGGCAA TTTTACGACG AAGATGGTGG AAGTACATGA TTTTGGGACT CATAGACCTG 
GAAGCAAATT ATCTGGTGGT CAAGGCTTAC CAATACACAA CTCTGACCAG TATCCAGCTC 
CTGGACTGTT TTGTGATCCC AGTCGTGATT TTGCTCTCCT GGTTCTTCCT GCTGATCCGG 
TACAAGGCTG TGCATTTCAT CGGCATCGTT GTCTGCATCC TGGGAATGGG CTGCATGGTG 
GGAGCAGATG TGCTTGTGGG AAGACATCAG GGAGCAGGGG AAAATAAGCT GGTAGGGGAC 
CTTCTGGTCT TAGGAGGAGC CACACTCTAT GGTATTTCTA ACGTCTGGGA AGAATACATC 
ATCCGAACTC TGAGCCGAGT GGAATTCCTG GGAATGATTG GTCTCTTTGG AGCATTTTTC 
AGTGGAATTC AATTAGCTAT AATGGAGCAT AAGGAACTGT TGAAGGTGCC CTGGGACTGG 
CAAATAGGAC TGCTCTACGT TGGCTTTAGT GCCTGCATGT TTGGTCTCTA CAGCTTTATG 
CCAGTCGTCA TAAAGAAAAC CAGTGCCACT TCAGTCAACC TCTCCTTGCT CACAGCAGAC 
TTGTACAGCC TGTTCTGTGG ATTGTTTCTC TTCCACTACA AGTTTTCAGG ACTTTATCTC 
CTGTCTTTCT TCACCATCCT CATTGGGCTG GTGCTCTACT CCTCCACCTC CACCTACATA 
GCCCAGGACC CCCGAGTGTA TAAGCAGTTC CGCAATCCTT CAGGACCTGT TGTGGACTTA 
CCGACCACAG CTCAGGTGGA ACCCTCAGTC ACCTACACCA GCCTGGGCCA GGAGACCGAA 
GAGGAGCCTC ATGTTCGTGT GGCCTAG

The stop codons will be deleted if pcDNA3.1⁺/C-(K)DYK vector is selected.

SLC35F1 ( XM_005266865.3 ) cDNA ORF clone, Homo sapiens(human) -> XP_005266922.1 Homo sapiens solute carrier family 35, member F1 (SLC35F1), transcript variant X1, mRNA.

Price & Availability↑

CloneID	OHu24322
Clone ID Related Accession (Same CDS sequence)	XM_005266865.3 , XM_005266865.4 , NM_001029858.3 , NM_001029858.4
Accession Version	XM_005266865.3	Documents for ORF clone product in default vector
Sequence Information	ORF Nucleotide Sequence (Length: 1227bp) Protein sequence SNP
Vector	pcDNA3.1-C-(k)DYK or customized vector	User Manual
Clone information	Clone Map	MSDS
Tag on pcDNA3.1⁺/C-(K)DYK	C terminal DYKDDDDK tags
ORF Insert Method	CloneEZ™ Seamless cloning technology
Insert Structure	linear
Update Date	2015-03-11
Organism	Homo sapiens(Human)
Product	solute carrier family 35 member F1 isoform X1
Comment

ATGATCCCCC CTGAGCAGCC GCAGCAGCAG CTGCAGCCGC CGTCGCCAGC CCCGCCGAAC 
CATGTGGTGA CCACCATCGA GAACCTGCCG GCCGAGGGCA GCGGCGGCGG CGGGAGCCTG 
TCCGCCTCCT CCCGGGCTGG CGTGCGCCAG AGGATCCGCA AAGTGCTGAA CAGGGAGATG 
TTAATCTCTG TGGCCCTAGG CCAGGTGTTA TCCCTCCTTA TTTGTGGAAT TGGCTTGACT 
AGCAAGTATC TGTCAGAAGA TTTCCACGCC AACACACCAG TCTTCCAGAG TTTCCTCAAT 
TACATTCTTC TCTTCTTGGT CTATACCACC ACACTAGCCG TCAGACAAGG AGAAGAAAAC 
CTCCTGGCAA TTTTACGACG AAGATGGTGG AAGTACATGA TTTTGGGACT CATAGACCTG 
GAAGCAAATT ATCTGGTGGT CAAGGCTTAC CAATACACAA CTCTGACCAG TATCCAGCTC 
CTGGACTGTT TTGTGATCCC AGTCGTGATT TTGCTCTCCT GGTTCTTCCT GCTGATCCGG 
TACAAGGCTG TGCATTTCAT CGGCATCGTT GTCTGCATCC TGGGAATGGG CTGCATGGTG 
GGAGCAGATG TGCTTGTGGG AAGACATCAG GGAGCAGGGG AAAATAAGCT GGTAGGGGAC 
CTTCTGGTCT TAGGAGGAGC CACACTCTAT GGTATTTCTA ACGTCTGGGA AGAATACATC 
ATCCGAACTC TGAGCCGAGT GGAATTCCTG GGAATGATTG GTCTCTTTGG AGCATTTTTC 
AGTGGAATTC AATTAGCTAT AATGGAGCAT AAGGAACTGT TGAAGGTGCC CTGGGACTGG 
CAAATAGGAC TGCTCTACGT TGGCTTTAGT GCCTGCATGT TTGGTCTCTA CAGCTTTATG 
CCAGTCGTCA TAAAGAAAAC CAGTGCCACT TCAGTCAACC TCTCCTTGCT CACAGCAGAC 
TTGTACAGCC TGTTCTGTGG ATTGTTTCTC TTCCACTACA AGTTTTCAGG ACTTTATCTC 
CTGTCTTTCT TCACCATCCT CATTGGGCTG GTGCTCTACT CCTCCACCTC CACCTACATA 
GCCCAGGACC CCCGAGTGTA TAAGCAGTTC CGCAATCCTT CAGGACCTGT TGTGGACTTA 
CCGACCACAG CTCAGGTGGA ACCCTCAGTC ACCTACACCA GCCTGGGCCA GGAGACCGAA 
GAGGAGCCTC ATGTTCGTGT GGCCTAG

The stop codons will be deleted if pcDNA3.1⁺/C-(K)DYK vector is selected.

RefSeq

XP_005266922.1

Translation

MIPPEQPQQQLQPPSPAPPNHVVTTIENLPAEGSGGGGSLSASSRAGVRQRIRKVLNREMLISVALGQVLSLLICGIGLTSKYLSEDFHANTPVFQSFLNYILLFLVYTTTLAVRQGEENLLAILRRRWWKYMILGLIDLEANYLVVKAYQYTTLTSIQLLDCFVIPVVILLSWFFLLIRYKAVHFIGIVVCILGMGCMVGADVLVGRHQGAGENKLVGDLLVLGGATLYGISNVWEEYIIRTLSRVEFLGMIGLFGAFFSGIQLAIMEHKELLKVPWDWQIGLLYVGFSACMFGLYSFMPVVIKKTSATSVNLSLLTADLYSLFCGLFLFHYKFSGLYLLSFFTILIGLVLYSSTSTYIAQDPRVYKQFRNPSGPVVDLPTTAQVEPSVTYTSLGQETEEEPHVRVA

Target ORF information:

RefSeq Version	XM_005266865.3
Organism	Homo sapiens(Human)
Definition	Homo sapiens solute carrier family 35, member F1 (SLC35F1), transcript variant X1, mRNA.

Target ORF information:

Epitope	DYKDDDDK
Bacterial selection	AMP^R
Mammalian selection	Neo^R
Vector	pcDNA3.1⁺/C-(K)DYK

XM_005266865.3

ORF Insert Sequence:

ATGATCCCCC CTGAGCAGCC GCAGCAGCAG CTGCAGCCGC CGTCGCCAGC CCCGCCGAAC 
CATGTGGTGA CCACCATCGA GAACCTGCCG GCCGAGGGCA GCGGCGGCGG CGGGAGCCTG 
TCCGCCTCCT CCCGGGCTGG CGTGCGCCAG AGGATCCGCA AAGTGCTGAA CAGGGAGATG 
TTAATCTCTG TGGCCCTAGG CCAGGTGTTA TCCCTCCTTA TTTGTGGAAT TGGCTTGACT 
AGCAAGTATC TGTCAGAAGA TTTCCACGCC AACACACCAG TCTTCCAGAG TTTCCTCAAT 
TACATTCTTC TCTTCTTGGT CTATACCACC ACACTAGCCG TCAGACAAGG AGAAGAAAAC 
CTCCTGGCAA TTTTACGACG AAGATGGTGG AAGTACATGA TTTTGGGACT CATAGACCTG 
GAAGCAAATT ATCTGGTGGT CAAGGCTTAC CAATACACAA CTCTGACCAG TATCCAGCTC 
CTGGACTGTT TTGTGATCCC AGTCGTGATT TTGCTCTCCT GGTTCTTCCT GCTGATCCGG 
TACAAGGCTG TGCATTTCAT CGGCATCGTT GTCTGCATCC TGGGAATGGG CTGCATGGTG 
GGAGCAGATG TGCTTGTGGG AAGACATCAG GGAGCAGGGG AAAATAAGCT GGTAGGGGAC 
CTTCTGGTCT TAGGAGGAGC CACACTCTAT GGTATTTCTA ACGTCTGGGA AGAATACATC 
ATCCGAACTC TGAGCCGAGT GGAATTCCTG GGAATGATTG GTCTCTTTGG AGCATTTTTC 
AGTGGAATTC AATTAGCTAT AATGGAGCAT AAGGAACTGT TGAAGGTGCC CTGGGACTGG 
CAAATAGGAC TGCTCTACGT TGGCTTTAGT GCCTGCATGT TTGGTCTCTA CAGCTTTATG 
CCAGTCGTCA TAAAGAAAAC CAGTGCCACT TCAGTCAACC TCTCCTTGCT CACAGCAGAC 
TTGTACAGCC TGTTCTGTGG ATTGTTTCTC TTCCACTACA AGTTTTCAGG ACTTTATCTC 
CTGTCTTTCT TCACCATCCT CATTGGGCTG GTGCTCTACT CCTCCACCTC CACCTACATA 
GCCCAGGACC CCCGAGTGTA TAAGCAGTTC CGCAATCCTT CAGGACCTGT TGTGGACTTA 
CCGACCACAG CTCAGGTGGA ACCCTCAGTC ACCTACACCA GCCTGGGCCA GGAGACCGAA 
GAGGAGCCTC ATGTTCGTGT GGCCTAG

The stop codons will be deleted if pcDNA3.1⁺/C-(K)DYK vector is selected.

SLC35F1 ( XM_005266865.4 ) cDNA ORF clone, Homo sapiens(human) -> XP_005266922.1 Homo sapiens solute carrier family 35 member F1 (SLC35F1), transcript variant X1, mRNA.

Price & Availability↑

CloneID	OHu24322
Clone ID Related Accession (Same CDS sequence)	XM_005266865.3 , XM_005266865.4 , NM_001029858.3 , NM_001029858.4
Accession Version	XM_005266865.4 Latest version!	Documents for ORF clone product in default vector
Sequence Information	ORF Nucleotide Sequence (Length: 1227bp) Protein sequence SNP
Vector	pcDNA3.1-C-(k)DYK or customized vector	User Manual
Clone information	Clone Map	MSDS
Tag on pcDNA3.1⁺/C-(K)DYK	C terminal DYKDDDDK tags
ORF Insert Method	CloneEZ™ Seamless cloning technology
Insert Structure	linear
Update Date	2019-12-05
Organism	Homo sapiens(human)
Product	solute carrier family 35 member F1 isoform X1
Comment	Comment: MODEL REFSEQ: This record is predicted by automated computational analysis. This record is derived from a genomic sequence (NC_000006.12) annotated using gene prediction method: Gnomon, supported by mRNA and EST evidence. Also see: Documentation of NCBI's Annotation Process On Jun 6, 2016 this sequence version replaced XM_005266865.3. ##Genome-Annotation-Data-START## Annotation Provider :: NCBI Annotation Status :: Updated annotation Annotation Name :: Homo sapiens Updated Annotation Release 109.20191205 Annotation Version :: 109.20191205 Annotation Pipeline :: NCBI eukaryotic genome annotation pipeline Annotation Software Version :: 8.3 Annotation Method :: Best-placed RefSeq; propagated RefSeq model Features Annotated :: Gene; mRNA; CDS; ncRNA ##Genome-Annotation-Data-END##

ATGATCCCCC CTGAGCAGCC GCAGCAGCAG CTGCAGCCGC CGTCGCCAGC CCCGCCGAAC 
CATGTGGTGA CCACCATCGA GAACCTGCCG GCCGAGGGCA GCGGCGGCGG CGGGAGCCTG 
TCCGCCTCCT CCCGGGCTGG CGTGCGCCAG AGGATCCGCA AAGTGCTGAA CAGGGAGATG 
TTAATCTCTG TGGCCCTAGG CCAGGTGTTA TCCCTCCTTA TTTGTGGAAT TGGCTTGACT 
AGCAAGTATC TGTCAGAAGA TTTCCACGCC AACACACCAG TCTTCCAGAG TTTCCTCAAT 
TACATTCTTC TCTTCTTGGT CTATACCACC ACACTAGCCG TCAGACAAGG AGAAGAAAAC 
CTCCTGGCAA TTTTACGACG AAGATGGTGG AAGTACATGA TTTTGGGACT CATAGACCTG 
GAAGCAAATT ATCTGGTGGT CAAGGCTTAC CAATACACAA CTCTGACCAG TATCCAGCTC 
CTGGACTGTT TTGTGATCCC AGTCGTGATT TTGCTCTCCT GGTTCTTCCT GCTGATCCGG 
TACAAGGCTG TGCATTTCAT CGGCATCGTT GTCTGCATCC TGGGAATGGG CTGCATGGTG 
GGAGCAGATG TGCTTGTGGG AAGACATCAG GGAGCAGGGG AAAATAAGCT GGTAGGGGAC 
CTTCTGGTCT TAGGAGGAGC CACACTCTAT GGTATTTCTA ACGTCTGGGA AGAATACATC 
ATCCGAACTC TGAGCCGAGT GGAATTCCTG GGAATGATTG GTCTCTTTGG AGCATTTTTC 
AGTGGAATTC AATTAGCTAT AATGGAGCAT AAGGAACTGT TGAAGGTGCC CTGGGACTGG 
CAAATAGGAC TGCTCTACGT TGGCTTTAGT GCCTGCATGT TTGGTCTCTA CAGCTTTATG 
CCAGTCGTCA TAAAGAAAAC CAGTGCCACT TCAGTCAACC TCTCCTTGCT CACAGCAGAC 
TTGTACAGCC TGTTCTGTGG ATTGTTTCTC TTCCACTACA AGTTTTCAGG ACTTTATCTC 
CTGTCTTTCT TCACCATCCT CATTGGGCTG GTGCTCTACT CCTCCACCTC CACCTACATA 
GCCCAGGACC CCCGAGTGTA TAAGCAGTTC CGCAATCCTT CAGGACCTGT TGTGGACTTA 
CCGACCACAG CTCAGGTGGA ACCCTCAGTC ACCTACACCA GCCTGGGCCA GGAGACCGAA 
GAGGAGCCTC ATGTTCGTGT GGCCTAG

The stop codons will be deleted if pcDNA3.1⁺/C-(K)DYK vector is selected.

RefSeq	XP_005266922.1
CDS	502..1728
Translation	MIPPEQPQQQLQPPSPAPPNHVVTTIENLPAEGSGGGGSLSASSRAGVRQRIRKVLNREMLISVALGQVLSLLICGIGLTSKYLSEDFHANTPVFQSFLNYILLFLVYTTTLAVRQGEENLLAILRRRWWKYMILGLIDLEANYLVVKAYQYTTLTSIQLLDCFVIPVVILLSWFFLLIRYKAVHFIGIVVCILGMGCMVGADVLVGRHQGAGENKLVGDLLVLGGATLYGISNVWEEYIIRTLSRVEFLGMIGLFGAFFSGIQLAIMEHKELLKVPWDWQIGLLYVGFSACMFGLYSFMPVVIKKTSATSVNLSLLTADLYSLFCGLFLFHYKFSGLYLLSFFTILIGLVLYSSTSTYIAQDPRVYKQFRNPSGPVVDLPTTAQVEPSVTYTSLGQETEEEPHVRVA

Target ORF information:

RefSeq Version	XM_005266865.4
Organism	Homo sapiens(human)
Definition	Homo sapiens solute carrier family 35 member F1 (SLC35F1), transcript variant X1, mRNA.

Target ORF information:

Epitope	DYKDDDDK
Bacterial selection	AMP^R
Mammalian selection	Neo^R
Vector	pcDNA3.1⁺/C-(K)DYK

XM_005266865.4

ORF Insert Sequence:

ATGATCCCCC CTGAGCAGCC GCAGCAGCAG CTGCAGCCGC CGTCGCCAGC CCCGCCGAAC 
CATGTGGTGA CCACCATCGA GAACCTGCCG GCCGAGGGCA GCGGCGGCGG CGGGAGCCTG 
TCCGCCTCCT CCCGGGCTGG CGTGCGCCAG AGGATCCGCA AAGTGCTGAA CAGGGAGATG 
TTAATCTCTG TGGCCCTAGG CCAGGTGTTA TCCCTCCTTA TTTGTGGAAT TGGCTTGACT 
AGCAAGTATC TGTCAGAAGA TTTCCACGCC AACACACCAG TCTTCCAGAG TTTCCTCAAT 
TACATTCTTC TCTTCTTGGT CTATACCACC ACACTAGCCG TCAGACAAGG AGAAGAAAAC 
CTCCTGGCAA TTTTACGACG AAGATGGTGG AAGTACATGA TTTTGGGACT CATAGACCTG 
GAAGCAAATT ATCTGGTGGT CAAGGCTTAC CAATACACAA CTCTGACCAG TATCCAGCTC 
CTGGACTGTT TTGTGATCCC AGTCGTGATT TTGCTCTCCT GGTTCTTCCT GCTGATCCGG 
TACAAGGCTG TGCATTTCAT CGGCATCGTT GTCTGCATCC TGGGAATGGG CTGCATGGTG 
GGAGCAGATG TGCTTGTGGG AAGACATCAG GGAGCAGGGG AAAATAAGCT GGTAGGGGAC 
CTTCTGGTCT TAGGAGGAGC CACACTCTAT GGTATTTCTA ACGTCTGGGA AGAATACATC 
ATCCGAACTC TGAGCCGAGT GGAATTCCTG GGAATGATTG GTCTCTTTGG AGCATTTTTC 
AGTGGAATTC AATTAGCTAT AATGGAGCAT AAGGAACTGT TGAAGGTGCC CTGGGACTGG 
CAAATAGGAC TGCTCTACGT TGGCTTTAGT GCCTGCATGT TTGGTCTCTA CAGCTTTATG 
CCAGTCGTCA TAAAGAAAAC CAGTGCCACT TCAGTCAACC TCTCCTTGCT CACAGCAGAC 
TTGTACAGCC TGTTCTGTGG ATTGTTTCTC TTCCACTACA AGTTTTCAGG ACTTTATCTC 
CTGTCTTTCT TCACCATCCT CATTGGGCTG GTGCTCTACT CCTCCACCTC CACCTACATA 
GCCCAGGACC CCCGAGTGTA TAAGCAGTTC CGCAATCCTT CAGGACCTGT TGTGGACTTA 
CCGACCACAG CTCAGGTGGA ACCCTCAGTC ACCTACACCA GCCTGGGCCA GGAGACCGAA 
GAGGAGCCTC ATGTTCGTGT GGCCTAG

The stop codons will be deleted if pcDNA3.1⁺/C-(K)DYK vector is selected.

PubMed

Genetic association study of QT interval highlights role for calcium signaling pathways in myocardial repolarization.
Nature genetics46(8)826-36(2014 Aug)
Arking DE,Pulit SL,Crotti L,van der Harst P,Munroe PB,Koopmann TT,Sotoodehnia N,Rossin EJ,Morley M,Wang X,Johnson AD,Lundby A,Gudbjartsson DF,Noseworthy PA,Eijgelsheim M,Bradford Y,Tarasov KV,D?rr M,M?ller-Nurasyid M,Lahtinen AM,Nolte IM,Smith AV,Bis JC,Isaacs A,Newhouse SJ,Evans DS,Post WS,Waggott D,Lyytik?inen LP,Hicks AA,Eisele L,Ellinghaus D,Hayward C,Navarro P,Ulivi S,Tanaka T,Tester DJ,Chatel S,Gustafsson S,Kumari M,Morris RW,Naluai ?T,Padmanabhan S,Kluttig A,Strohmer B,Panayiotou AG,Torres M,Knoflach M,Hubacek JA,Slowikowski K,Raychaudhuri S,Kumar RD,Harris TB,Launer LJ,Shuldiner AR,Alonso A,Bader JS,Ehret G,Huang H,Kao WH,Strait JB,Macfarlane PW,Brown M,Caulfield MJ,Samani NJ,Kronenberg F,Willeit J,,,Smith JG,Greiser KH,Meyer Zu Schwabedissen H,Werdan K,Carella M,Zelante L,Heckbert SR,Psaty BM,Rotter JI,Kolcic I,Pola?ek O,Wright AF,Griffin M,Daly MJ,,Arnar DO,H?lm H,Thorsteinsdottir U,,Denny JC,Roden DM,Zuvich RL,Emilsson V,Plump AS,Larson MG,O'Donnell CJ,Yin X,Bobbo M,D'Adamo AP,Iorio A,Sinagra G,Carracedo A,Cummings SR,Nalls MA,Jula A,Kontula KK,Marjamaa A,Oikarinen L,Perola M,Porthan K,Erbel R,Hoffmann P,J?ckel KH,K?lsch H,N?then MM,,den Hoed M,Loos RJ,Thelle DS,Gieger C,Meitinger T,Perz S,Peters A,Prucha H,Sinner MF,Waldenberger M,de Boer RA,Franke L,van der Vleuten PA,Beckmann BM,Martens E,Bardai A,Hofman N,Wilde AA,Behr ER,Dalageorgou C,Giudicessi JR,Medeiros-Domingo A,Barc J,Kyndt F,Probst V,Ghidoni A,Insolia R,Hamilton RM,Scherer SW,Brandimarto J,Margulies K,Moravec CE,del Greco M F,Fuchsberger C,O'Connell JR,Lee WK,Watt GC,Campbell H,Wild SH,El Mokhtari NE,Frey N,Asselbergs FW,Mateo Leach I,Navis G,van den Berg MP,van Veldhuisen DJ,Kellis M,Krijthe BP,Franco OH,Hofman A,Kors JA,Uitterlinden AG,Witteman JC,Kedenko L,Lamina C,Oostra BA,Abecasis GR,Lakatta EG,Mulas A,Orr? M,Schlessinger D,Uda M,Markus MR,V?lker U,Snieder H,Spector TD,?rnl?v J,Lind L,Sundstr?m J,Syv?nen AC,Kivimaki M,K?h?nen M,Mononen N,Raitakari OT,Viikari JS,Adamkova V,Kiechl S,Brion M,Nicolaides AN,Paulweber B,Haerting J,Dominiczak AF,Nyberg F,Whincup PH,Hingorani AD,Schott JJ,Bezzina CR,Ingelsson E,Ferrucci L,Gasparini P,Wilson JF,Rudan I,Franke A,M?hleisen TW,Pramstaller PP,Lehtim?ki TJ,Paterson AD,Parsa A,Liu Y,van Duijn CM,Siscovick DS,Gudnason V,Jamshidi Y,Salomaa V,Felix SB,Sanna S,Ritchie MD,Stricker BH,Stefansson K,Boyer LA,Cappola TP,Olsen JV,Lage K,Schwartz PJ,K??b S,Chakravarti A,Ackerman MJ,Pfeufer A,de Bakker PI,Newton-Cheh C

Genome-wide association analyses suggest NELL1 influences adverse metabolic response to HCTZ in African Americans.
The pharmacogenomics journal14(1)35-40(2014 Feb)
Del-Aguila JL,Beitelshees AL,Cooper-Dehoff RM,Chapman AB,Gums JG,Bailey K,Gong Y,Turner ST,Johnson JA,Boerwinkle E

Identification of heart rate-associated loci and their effects on cardiac conduction and rhythm disorders.
Nature genetics45(6)621-31(2013 Jun)
den Hoed M,Eijgelsheim M,Esko T,Brundel BJ,Peal DS,Evans DM,Nolte IM,Segr? AV,Holm H,Handsaker RE,Westra HJ,Johnson T,Isaacs A,Yang J,Lundby A,Zhao JH,Kim YJ,Go MJ,Almgren P,Bochud M,Boucher G,Cornelis MC,Gudbjartsson D,Hadley D,van der Harst P,Hayward C,den Heijer M,Igl W,Jackson AU,Kutalik Z,Luan J,Kemp JP,Kristiansson K,Ladenvall C,Lorentzon M,Montasser ME,Njajou OT,O'Reilly PF,Padmanabhan S,St Pourcain B,Rankinen T,Salo P,Tanaka T,Timpson NJ,Vitart V,Waite L,Wheeler W,Zhang W,Draisma HH,Feitosa MF,Kerr KF,Lind PA,Mihailov E,Onland-Moret NC,Song C,Weedon MN,Xie W,Yengo L,Absher D,Albert CM,Alonso A,Arking DE,de Bakker PI,Balkau B,Barlassina C,Benaglio P,Bis JC,Bouatia-Naji N,Brage S,Chanock SJ,Chines PS,Chung M,Darbar D,Dina C,D?rr M,Elliott P,Felix SB,Fischer K,Fuchsberger C,de Geus EJ,Goyette P,Gudnason V,Harris TB,Hartikainen AL,Havulinna AS,Heckbert SR,Hicks AA,Hofman A,Holewijn S,Hoogstra-Berends F,Hottenga JJ,Jensen MK,Johansson A,Junttila J,K??b S,Kanon B,Ketkar S,Khaw KT,Knowles JW,Kooner AS,Kors JA,Kumari M,Milani L,Laiho P,Lakatta EG,Langenberg C,Leusink M,Liu Y,Luben RN,Lunetta KL,Lynch SN,Markus MR,Marques-Vidal P,Mateo Leach I,McArdle WL,McCarroll SA,Medland SE,Miller KA,Montgomery GW,Morrison AC,M?ller-Nurasyid M,Navarro P,Nelis M,O'Connell JR,O'Donnell CJ,Ong KK,Newman AB,Peters A,Polasek O,Pouta A,Pramstaller PP,Psaty BM,Rao DC,Ring SM,Rossin EJ,Rudan D,Sanna S,Scott RA,Sehmi JS,Sharp S,Shin JT,Singleton AB,Smith AV,Soranzo N,Spector TD,Stewart C,Stringham HM,Tarasov KV,Uitterlinden AG,Vandenput L,Hwang SJ,Whitfield JB,Wijmenga C,Wild SH,Willemsen G,Wilson JF,Witteman JC,Wong A,Wong Q,Jamshidi Y,Zitting P,Boer JM,Boomsma DI,Borecki IB,van Duijn CM,Ekelund U,Forouhi NG,Froguel P,Hingorani A,Ingelsson E,Kivimaki M,Kronmal RA,Kuh D,Lind L,Martin NG,Oostra BA,Pedersen NL,Quertermous T,Rotter JI,van der Schouw YT,Verschuren WM,Walker M,Albanes D,Arnar DO,Assimes TL,Bandinelli S,Boehnke M,de Boer RA,Bouchard C,Caulfield WL,Chambers JC,Curhan G,Cusi D,Eriksson J,Ferrucci L,van Gilst WH,Glorioso N,de Graaf J,Groop L,Gyllensten U,Hsueh WC,Hu FB,Huikuri HV,Hunter DJ,Iribarren C,Isomaa B,Jarvelin MR,Jula A,K?h?nen M,Kiemeney LA,van der Klauw MM,Kooner JS,Kraft P,Iacoviello L,Lehtim?ki T,Lokki ML,Mitchell BD,Navis G,Nieminen MS,Ohlsson C,Poulter NR,Qi L,Raitakari OT,Rimm EB,Rioux JD,Rizzi F,Rudan I,Salomaa V,Sever PS,Shields DC,Shuldiner AR,Sinisalo J,Stanton AV,Stolk RP,Strachan DP,Tardif JC,Thorsteinsdottir U,Tuomilehto J,van Veldhuisen DJ,Virtamo J,Viikari J,Vollenweider P,Waeber G,Widen E,Cho YS,Olsen JV,Visscher PM,Willer C,Franke L,,,Erdmann J,Thompson JR,,Pfeufer A,,Sotoodehnia N,,Newton-Cheh C,,Ellinor PT,Stricker BH,Metspalu A,Perola M,Beckmann JS,Smith GD,Stefansson K,Wareham NJ,Munroe PB,Sibon OC,Milan DJ,Snieder H,Samani NJ,Loos RJ

Genome-wide association analysis identifies multiple loci related to resting heart rate.
Human molecular genetics19(19)3885-94(2010 Oct)
Eijgelsheim M,Newton-Cheh C,Sotoodehnia N,de Bakker PI,M?ller M,Morrison AC,Smith AV,Isaacs A,Sanna S,D?rr M,Navarro P,Fuchsberger C,Nolte IM,de Geus EJ,Estrada K,Hwang SJ,Bis JC,R?ckert IM,Alonso A,Launer LJ,Hottenga JJ,Rivadeneira F,Noseworthy PA,Rice KM,Perz S,Arking DE,Spector TD,Kors JA,Aulchenko YS,Tarasov KV,Homuth G,Wild SH,Marroni F,Gieger C,Licht CM,Prineas RJ,Hofman A,Rotter JI,Hicks AA,Ernst F,Najjar SS,Wright AF,Peters A,Fox ER,Oostra BA,Kroemer HK,Couper D,V?lzke H,Campbell H,Meitinger T,Uda M,Witteman JC,Psaty BM,Wichmann HE,Harris TB,K??b S,Siscovick DS,Jamshidi Y,Uitterlinden AG,Folsom AR,Larson MG,Wilson JF,Penninx BW,Snieder H,Pramstaller PP,van Duijn CM,Lakatta EG,Felix SB,Gudnason V,Pfeufer A,Heckbert SR,Stricker BH,Boerwinkle E,O'Donnell CJ

Genome-wide pleiotropy of osteoporosis-related phenotypes: the Framingham Study.
Journal of bone and mineral research : the official journal of the American Society for Bone and Mineral Research25(7)1555-63(2010 Jul)
Karasik D,Hsu YH,Zhou Y,Cupples LA,Kiel DP,Demissie S

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SLC35F1 cDNA ORF clone, Homo sapiens(human)

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Target ORF information:

ORF Insert Sequence:

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Target ORF information:

ORF Insert Sequence:

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