ANXA9 cDNA ORF clone, Homo sapiens(human)

Gene
Clones
gRNAs

Summary

Gene Symbol	ANXA9
Entrez Gene ID	8416
Full Name	annexin A9
Synonyms	ANX31
General protein information	Preferred Names annexin A9 Names annexin A9 annexin 31 annexin XXXI annexin-9 pemphaxin
Gene Type	protein-coding
Organism	Homo sapiens(human)
Genome	Chromosome: 1 Map Location: 1q21.3
Summary	The annexins are a family of calcium-dependent phospholipid-binding proteins. Members of the annexin family contain 4 internal repeat domains, each of which includes a type II calcium-binding site. The calcium-binding sites are required for annexins to aggregate and cooperatively bind anionic phospholipids and extracellular matrix proteins. This gene encodes a divergent member of the annexin protein family in which all four homologous type II calcium-binding sites in the conserved tetrad core contain amino acid substitutions that ablate their function. However, structural analysis suggests that the conserved putative ion channel formed by the tetrad core is intact. [provided by RefSeq, Jul 2008].
Disorder MIM:	603319

mRNA and Protein(s)

mRNA	Protein	Name
NM_003568.3	NP_003559.2	annexin A9
XM_011510058.2	XP_011508360.1	annexin A9 isoform X1
XM_011510058.3	XP_011508360.1	annexin A9 isoform X1
NM_003568.2	NP_003559.2	annexin A9

Pathways from BioSystems

Homologies

Homo sapiens (human)	ANXA9	NP_003559.2
Rattus norvegicus (Norway rat)	Anxa9	XP_001072193.3
Pan troglodytes (chimpanzee)	ANXA9	XP_513782.2
	ANXA9	XP_001103401.1
Bos taurus (cattle)	ANXA9	NP_001030450.1
Mus musculus (house mouse)	Anxa9	NP_076117.2
Canis lupus familiaris (dog)	ANXA9	XP_850397.1
Xenopus tropicalis (tropical clawed frog)	anxa9	NP_001008048.1

Gene Ontology
Bibliography

Related articles in PubMed

Discovery and refinement of loci associated with lipid levels.
Willer CJ, Schmidt EM, Sengupta S, Peloso GM, Gustafsson S, Kanoni S, Ganna A, Chen J, Buchkovich ML, Mora S, Beckmann JS, Bragg-Gresham JL, Chang HY, Demirkan A, Den Hertog HM, Do R, Donnelly LA, Ehret GB, Esko T, Feitosa MF, Ferreira T, Fischer K, Fontanillas P, Fraser RM, Freitag DF, Gurdasani D, Heikkil? K, Hypp?nen E, Isaacs A, Jackson AU, Johansson ?, Johnson T, Kaakinen M, Kettunen J, Kleber ME, Li X, Luan J, Lyytik?inen LP, Magnusson PKE, Mangino M, Mihailov E, Montasser ME, M?ller-Nurasyid M, Nolte IM, O'Connell JR, Palmer CD, Perola M, Petersen AK, Sanna S, Saxena R, Service SK, Shah S, Shungin D, Sidore C, Song C, Strawbridge RJ, Surakka I, Tanaka T, Teslovich TM, Thorleifsson G, Van den Herik EG, Voight BF, Volcik KA, Waite LL, Wong A, Wu Y, Zhang W, Absher D, Asiki G, Barroso I, Been LF, Bolton JL, Bonnycastle LL, Brambilla P, Burnett MS, Cesana G, Dimitriou M, Doney ASF, D?ring A, Elliott P, Epstein SE, Ingi Eyjolfsson G, Gigante B, Goodarzi MO, Grallert H, Gravito ML, Groves CJ, Hallmans G, Hartikainen AL, Hayward C, Hernandez D, Hicks AA, Holm H, Hung YJ, Illig T, Jones MR, Kaleebu P, Kastelein JJP, Khaw KT, Kim E, Klopp N, Komulainen P, Kumari M, Langenberg C, Lehtim?ki T, Lin SY, Lindstr?m J, Loos RJF, Mach F, McArdle WL, Meisinger C, Mitchell BD, M?ller G, Nagaraja R, Narisu N, Nieminen TVM, Nsubuga RN, Olafsson I, Ong KK, Palotie A, Papamarkou T, Pomilla C, Pouta A, Rader DJ, Reilly MP, Ridker PM, Rivadeneira F, Rudan I, Ruokonen A, Samani N, Scharnagl H, Seeley J, Silander K, Stan??kov? A, Stirrups K, Swift AJ, Tiret L, Uitterlinden AG, van Pelt LJ, Vedantam S, Wainwright N, Wijmenga C, Wild SH, Willemsen G, Wilsgaard T, Wilson JF, Young EH, Zhao JH, Adair LS, Arveiler D, Assimes TL, Bandinelli S, Bennett F, Bochud M, Boehm BO, Boomsma DI, Borecki IB, Bornstein SR, Bovet P, Burnier M, Campbell H, Chakravarti A, Chambers JC, Chen YI, Collins FS, Cooper RS, Danesh J, Dedoussis G, de Faire U, Feranil AB, Ferri?res J, Ferrucci L, Freimer NB, Gieger C, Groop LC, Gudnason V, Gyllensten U, Hamsten A, Harris TB, Hingorani A, Hirschhorn JN, Hofman A, Hovingh GK, Hsiung CA, Humphries SE, Hunt SC, Hveem K, Iribarren C, J?rvelin MR, Jula A, K?h?nen M, Kaprio J, Kes?niemi A, Kivimaki M, Kooner JS, Koudstaal PJ, Krauss RM, Kuh D, Kuusisto J, Kyvik KO, Laakso M, Lakka TA, Lind L, Lindgren CM, Martin NG, M?rz W, McCarthy MI, McKenzie CA, Meneton P, Metspalu A, Moilanen L, Morris AD, Munroe PB, Nj?lstad I, Pedersen NL, Power C, Pramstaller PP, Price JF, Psaty BM, Quertermous T, Rauramaa R, Saleheen D, Salomaa V, Sanghera DK, Saramies J, Schwarz PEH, Sheu WH, Shuldiner AR, Siegbahn A, Spector TD, Stefansson K, Strachan DP, Tayo BO, Tremoli E, Tuomilehto J, Uusitupa M, van Duijn CM, Vollenweider P, Wallentin L, Wareham NJ, Whitfield JB, Wolffenbuttel BHR, Ordovas JM, Boerwinkle E, Palmer CNA, Thorsteinsdottir U, Chasman DI, Rotter JI, Franks PW, Ripatti S, Cupples LA, Sandhu MS, Rich SS, Boehnke M, Deloukas P, Kathiresan S, Mohlke KL, Ingelsson E, Abecasis GR,
Nature genetics45(11)1274-1283(2013 Nov)

Genome-wide association study identifies genetic risk underlying primary rhegmatogenous retinal detachment.
Kirin M, Chandra A, Charteris DG, Hayward C, Campbell S, Celap I, Bencic G, Vatavuk Z, Kirac I, Richards AJ, Tenesa A, Snead MP, Fleck BW, Singh J, Harsum S, Maclaren RE, den Hollander AI, Dunlop MG, Hoyng CB, Wright AF, Campbell H, Vitart V, Mitry D
Human molecular genetics22(15)3174-85(2013 Aug)

Annexin A9 is a periplakin interacting partner in membrane-targeted cytoskeletal linker protein complexes.
Boczonadi V, M??tt? A
FEBS letters586(19)3090-6(2012 Sep)

Genome-wide association study identifies a new melanoma susceptibility locus at 1q21.3.
Macgregor S, Montgomery GW, Liu JZ, Zhao ZZ, Henders AK, Stark M, Schmid H, Holland EA, Duffy DL, Zhang M, Painter JN, Nyholt DR, Maskiell JA, Jetann J, Ferguson M, Cust AE, Jenkins MA, Whiteman DC, Olsson H, Puig S, Bianchi-Scarr? G, Hansson J, Demenais F, Landi MT, D?bniak T, Mackie R, Azizi E, Bressac-de Paillerets B, Goldstein AM, Kanetsky PA, Gruis NA, Elder DE, Newton-Bishop JA, Bishop DT, Iles MM, Helsing P, Amos CI, Wei Q, Wang LE, Lee JE, Qureshi AA, Kefford RF, Giles GG, Armstrong BK, Aitken JF, Han J, Hopper JL, Trent JM, Brown KM, Martin NG, Mann GJ, Hayward NK
Nature genetics43(11)1114-8(2011 Oct)

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

Annexin A9 and periplakin co-localise in the epidermis and annexin A9 is up-regulated in differentiating keratinocytes, but the epidermal annexin A9 expression does not require periplakin.
Title: Annexin A9 is a periplakin interacting partner in membrane-targeted cytoskeletal linker protein complexes.

examination of atypical properties
Title: Atypical properties displayed by annexin A9, a novel member of the annexin family of Ca(2+) and lipid binding proteins.

The following ANXA9 gene cDNA ORF clone sequences were retrieved from the NCBI Reference Sequence Database (RefSeq). These sequences represent the protein coding region of the ANXA9 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)
OHu24958	NM_003568.3 Latest version!	Homo sapiens annexin A9 (ANXA9), mRNA.	pcDNA3.1-C-(k)DYK or customized vector	in pcDNA3.1-C-(k)DYK	$159.50-$223.30 $319.00
OHu61750	XM_011510058.3 Latest version!	Homo sapiens annexin A9 (ANXA9), transcript variant X1, mRNA.	pcDNA3.1-C-(k)DYK or customized vector	7-9	$139.30 $199.00
View Old Accession Versions >>
OHu61750	XM_011510058.2	Homo sapiens annexin A9 (ANXA9), transcript variant X1, mRNA.	pcDNA3.1-C-(k)DYK or customized vector	7-9	$139.30 $199.00
OHu24958	NM_003568.2	Homo sapiens annexin A9 (ANXA9), mRNA.	pcDNA3.1-C-(k)DYK or customized vector	7-9	$69.30 $99.00
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)

ANXA9 ( NM_003568.3 ) cDNA ORF clone, Homo sapiens(human) -> NP_003559.2 Homo sapiens annexin A9 (ANXA9), mRNA.

Price & Availability↑

CloneID	OHu24958
Clone ID Related Accession (Same CDS sequence)	NM_003568.3 , NM_003568.2
Accession Version	NM_003568.3 Latest version!	Documents for ORF clone product in default vector
Sequence Information	ORF Nucleotide Sequence (Length: 1038bp) 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	2019-08-06
Organism	Homo sapiens(human)
Product	annexin A9
Comment	Comment: VALIDATED REFSEQ: This record has undergone validation or preliminary review. The reference sequence was derived from BJ993162.1, BC005830.2 and AJ009985.1. On Nov 22, 2018 this sequence version replaced NM_003568.2. Publication Note: This RefSeq record includes a subset of the publications that are available for this gene. Please see the Gene record to access additional publications. ##Evidence-Data-START## Transcript exon combination :: AJ009985.1, SRR5189661.83590.1 [ECO:0000332] RNAseq introns :: single sample supports all introns SAMEA1970526, SAMEA2144120 [ECO:0000348] ##Evidence-Data-END## ##RefSeq-Attributes-START## MANE Ensembl match :: ENST00000368947.9/ ENSP00000357943.4 RefSeq Select criteria :: based on conservation, expression, longest protein ##RefSeq-Attributes-END## COMPLETENESS: full length.

ATGTCTGTGA CTGGCGGGAA GATGGCACCG TCCCTCACCC AGGAGATCCT CAGCCACCTG 
GGCCTGGCCA GCAAGACTGC AGCGTGGGGG ACCCTGGGCA CCCTCAGGAC CTTCTTGAAC 
TTCAGCGTGG ACAAGGATGC GCAGAGGCTA CTGAGGGCCA TTACTGGCCA AGGCGTGGAC 
CGCAGTGCCA TTGTGGACGT GCTGACCAAC CGGAGCAGAG AGCAAAGGCA GCTCATCTCA 
CGAAACTTCC AGGAGCGCAC CCAACAGGAC CTGATGAAGT CTCTACAGGC AGCACTTTCC 
GGCAACCTGG AGAGGATTGT GATGGCTCTG CTGCAGCCCA CAGCCCAGTT TGACGCCCAG 
GAATTGAGGA CAGCTCTGAA GGCCTCAGAT TCTGCTGTGG ACGTGGCCAT TGAAATTCTT 
GCCACTCGAA CCCCACCCCA GCTGCAGGAG TGCCTGGCAG TCTACAAACA CAATTTCCAG 
GTGGAGGCTG TGGATGACAT CACATCTGAG ACCAGTGGCA TCTTGCAGGA CCTGCTGTTG 
GCCCTGGCCA AGGGGGGCCG TGACAGCTAC TCTGGAATCA TTGACTATAA TCTGGCAGAA 
CAAGATGTCC AGGCACTGCA GCGGGCAGAA GGACCTAGCA GAGAGGAAAC ATGGGTCCCA 
GTCTTCACCC AGCGAAATCC TGAACACCTC ATCCGAGTGT TTGATCAGTA CCAGCGGAGC 
ACTGGGCAAG AGCTGGAGGA GGCTGTCCAG AACCGTTTCC ATGGAGATGC TCAGGTGGCT 
CTGCTCGGCC TAGCTTCGGT GATCAAGAAC ACACCGCTGT ACTTTGCTGA CAAACTTCAT 
CAAGCCCTCC AGGAAACTGA GCCCAATTAC CAAGTCCTGA TTCGCATCCT TATCTCTCGA 
TGTGAGACTG ACCTTCTGAG TATCAGAGCT GAGTTCAGGA AGAAATTTGG GAAGTCCCTC 
TACTCTTCTC TCCAGGATGC AGTGAAAGGG GATTGCCAGT CAGCCCTCCT GGCCTTGTGC 
AGGGCTGAAG ACATGTGA

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

RefSeq	NP_003559.2
CDS	202..1239
Translation	MSVTGGKMAPSLTQEILSHLGLASKTAAWGTLGTLRTFLNFSVDKDAQRLLRAITGQGVDRSAIVDVLTNRSREQRQLISRNFQERTQQDLMKSLQAALSGNLERIVMALLQPTAQFDAQELRTALKASDSAVDVAIEILATRTPPQLQECLAVYKHNFQVEAVDDITSETSGILQDLLLALAKGGRDSYSGIIDYNLAEQDVQALQRAEGPSREETWVPVFTQRNPEHLIRVFDQYQRSTGQELEEAVQNRFHGDAQVALLGLASVIKNTPLYFADKLHQALQETEPNYQVLIRILISRCETDLLSIRAEFRKKFGKSLYSSLQDAVKGDCQSALLALCRAEDM

Target ORF information:

RefSeq Version	NM_003568.3
Organism	Homo sapiens(human)
Definition	Homo sapiens annexin A9 (ANXA9), mRNA.

Target ORF information:

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

NM_003568.3

ORF Insert Sequence:

ATGTCTGTGA CTGGCGGGAA GATGGCACCG TCCCTCACCC AGGAGATCCT CAGCCACCTG 
GGCCTGGCCA GCAAGACTGC AGCGTGGGGG ACCCTGGGCA CCCTCAGGAC CTTCTTGAAC 
TTCAGCGTGG ACAAGGATGC GCAGAGGCTA CTGAGGGCCA TTACTGGCCA AGGCGTGGAC 
CGCAGTGCCA TTGTGGACGT GCTGACCAAC CGGAGCAGAG AGCAAAGGCA GCTCATCTCA 
CGAAACTTCC AGGAGCGCAC CCAACAGGAC CTGATGAAGT CTCTACAGGC AGCACTTTCC 
GGCAACCTGG AGAGGATTGT GATGGCTCTG CTGCAGCCCA CAGCCCAGTT TGACGCCCAG 
GAATTGAGGA CAGCTCTGAA GGCCTCAGAT TCTGCTGTGG ACGTGGCCAT TGAAATTCTT 
GCCACTCGAA CCCCACCCCA GCTGCAGGAG TGCCTGGCAG TCTACAAACA CAATTTCCAG 
GTGGAGGCTG TGGATGACAT CACATCTGAG ACCAGTGGCA TCTTGCAGGA CCTGCTGTTG 
GCCCTGGCCA AGGGGGGCCG TGACAGCTAC TCTGGAATCA TTGACTATAA TCTGGCAGAA 
CAAGATGTCC AGGCACTGCA GCGGGCAGAA GGACCTAGCA GAGAGGAAAC ATGGGTCCCA 
GTCTTCACCC AGCGAAATCC TGAACACCTC ATCCGAGTGT TTGATCAGTA CCAGCGGAGC 
ACTGGGCAAG AGCTGGAGGA GGCTGTCCAG AACCGTTTCC ATGGAGATGC TCAGGTGGCT 
CTGCTCGGCC TAGCTTCGGT GATCAAGAAC ACACCGCTGT ACTTTGCTGA CAAACTTCAT 
CAAGCCCTCC AGGAAACTGA GCCCAATTAC CAAGTCCTGA TTCGCATCCT TATCTCTCGA 
TGTGAGACTG ACCTTCTGAG TATCAGAGCT GAGTTCAGGA AGAAATTTGG GAAGTCCCTC 
TACTCTTCTC TCCAGGATGC AGTGAAAGGG GATTGCCAGT CAGCCCTCCT GGCCTTGTGC 
AGGGCTGAAG ACATGTGA

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

ANXA9 ( NM_003568.2 ) cDNA ORF clone, Homo sapiens(human) -> NP_003559.2 Homo sapiens annexin A9 (ANXA9), mRNA.

Price & Availability↑

CloneID	OHu24958
Clone ID Related Accession (Same CDS sequence)	NM_003568.3 , NM_003568.2
Accession Version	NM_003568.2	Documents for ORF clone product in default vector
Sequence Information	ORF Nucleotide Sequence (Length: 1038bp) 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	annexin A9
Comment	Comment: VALIDATED REFSEQ: This record has undergone validation or preliminary review. The reference sequence was derived from BJ993162.1, BC005830.2 and AJ009985.1. On Apr 26, 2007 this sequence version replaced NM_003568.1. Publication Note: This RefSeq record includes a subset of the publications that are available for this gene. Please see the Gene record to access additional publications. ##Evidence-Data-START## Transcript exon combination :: BC005830.2, AJ009985.1 [ECO:0000332] RNAseq introns :: single sample supports all introns SAMEA1970526, SAMEA2144120 [ECO:0000348] ##Evidence-Data-END## COMPLETENESS: complete on the 3' end.

ATGTCTGTGA CTGGCGGGAA GATGGCACCG TCCCTCACCC AGGAGATCCT CAGCCACCTG 
GGCCTGGCCA GCAAGACTGC AGCGTGGGGG ACCCTGGGCA CCCTCAGGAC CTTCTTGAAC 
TTCAGCGTGG ACAAGGATGC GCAGAGGCTA CTGAGGGCCA TTACTGGCCA AGGCGTGGAC 
CGCAGTGCCA TTGTGGACGT GCTGACCAAC CGGAGCAGAG AGCAAAGGCA GCTCATCTCA 
CGAAACTTCC AGGAGCGCAC CCAACAGGAC CTGATGAAGT CTCTACAGGC AGCACTTTCC 
GGCAACCTGG AGAGGATTGT GATGGCTCTG CTGCAGCCCA CAGCCCAGTT TGACGCCCAG 
GAATTGAGGA CAGCTCTGAA GGCCTCAGAT TCTGCTGTGG ACGTGGCCAT TGAAATTCTT 
GCCACTCGAA CCCCACCCCA GCTGCAGGAG TGCCTGGCAG TCTACAAACA CAATTTCCAG 
GTGGAGGCTG TGGATGACAT CACATCTGAG ACCAGTGGCA TCTTGCAGGA CCTGCTGTTG 
GCCCTGGCCA AGGGGGGCCG TGACAGCTAC TCTGGAATCA TTGACTATAA TCTGGCAGAA 
CAAGATGTCC AGGCACTGCA GCGGGCAGAA GGACCTAGCA GAGAGGAAAC ATGGGTCCCA 
GTCTTCACCC AGCGAAATCC TGAACACCTC ATCCGAGTGT TTGATCAGTA CCAGCGGAGC 
ACTGGGCAAG AGCTGGAGGA GGCTGTCCAG AACCGTTTCC ATGGAGATGC TCAGGTGGCT 
CTGCTCGGCC TAGCTTCGGT GATCAAGAAC ACACCGCTGT ACTTTGCTGA CAAACTTCAT 
CAAGCCCTCC AGGAAACTGA GCCCAATTAC CAAGTCCTGA TTCGCATCCT TATCTCTCGA 
TGTGAGACTG ACCTTCTGAG TATCAGAGCT GAGTTCAGGA AGAAATTTGG GAAGTCCCTC 
TACTCTTCTC TCCAGGATGC AGTGAAAGGG GATTGCCAGT CAGCCCTCCT GGCCTTGTGC 
AGGGCTGAAG ACATGTGA

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

RefSeq	NP_003559.2
CDS	471..1508
Translation	MSVTGGKMAPSLTQEILSHLGLASKTAAWGTLGTLRTFLNFSVDKDAQRLLRAITGQGVDRSAIVDVLTNRSREQRQLISRNFQERTQQDLMKSLQAALSGNLERIVMALLQPTAQFDAQELRTALKASDSAVDVAIEILATRTPPQLQECLAVYKHNFQVEAVDDITSETSGILQDLLLALAKGGRDSYSGIIDYNLAEQDVQALQRAEGPSREETWVPVFTQRNPEHLIRVFDQYQRSTGQELEEAVQNRFHGDAQVALLGLASVIKNTPLYFADKLHQALQETEPNYQVLIRILISRCETDLLSIRAEFRKKFGKSLYSSLQDAVKGDCQSALLALCRAEDM

Target ORF information:

RefSeq Version	NM_003568.2
Organism	Homo sapiens(human)
Definition	Homo sapiens annexin A9 (ANXA9), mRNA.

Target ORF information:

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

NM_003568.2

ORF Insert Sequence:

ATGTCTGTGA CTGGCGGGAA GATGGCACCG TCCCTCACCC AGGAGATCCT CAGCCACCTG 
GGCCTGGCCA GCAAGACTGC AGCGTGGGGG ACCCTGGGCA CCCTCAGGAC CTTCTTGAAC 
TTCAGCGTGG ACAAGGATGC GCAGAGGCTA CTGAGGGCCA TTACTGGCCA AGGCGTGGAC 
CGCAGTGCCA TTGTGGACGT GCTGACCAAC CGGAGCAGAG AGCAAAGGCA GCTCATCTCA 
CGAAACTTCC AGGAGCGCAC CCAACAGGAC CTGATGAAGT CTCTACAGGC AGCACTTTCC 
GGCAACCTGG AGAGGATTGT GATGGCTCTG CTGCAGCCCA CAGCCCAGTT TGACGCCCAG 
GAATTGAGGA CAGCTCTGAA GGCCTCAGAT TCTGCTGTGG ACGTGGCCAT TGAAATTCTT 
GCCACTCGAA CCCCACCCCA GCTGCAGGAG TGCCTGGCAG TCTACAAACA CAATTTCCAG 
GTGGAGGCTG TGGATGACAT CACATCTGAG ACCAGTGGCA TCTTGCAGGA CCTGCTGTTG 
GCCCTGGCCA AGGGGGGCCG TGACAGCTAC TCTGGAATCA TTGACTATAA TCTGGCAGAA 
CAAGATGTCC AGGCACTGCA GCGGGCAGAA GGACCTAGCA GAGAGGAAAC ATGGGTCCCA 
GTCTTCACCC AGCGAAATCC TGAACACCTC ATCCGAGTGT TTGATCAGTA CCAGCGGAGC 
ACTGGGCAAG AGCTGGAGGA GGCTGTCCAG AACCGTTTCC ATGGAGATGC TCAGGTGGCT 
CTGCTCGGCC TAGCTTCGGT GATCAAGAAC ACACCGCTGT ACTTTGCTGA CAAACTTCAT 
CAAGCCCTCC AGGAAACTGA GCCCAATTAC CAAGTCCTGA TTCGCATCCT TATCTCTCGA 
TGTGAGACTG ACCTTCTGAG TATCAGAGCT GAGTTCAGGA AGAAATTTGG GAAGTCCCTC 
TACTCTTCTC TCCAGGATGC AGTGAAAGGG GATTGCCAGT CAGCCCTCCT GGCCTTGTGC 
AGGGCTGAAG ACATGTGA

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

ANXA9 ( XM_011510058.2 ) cDNA ORF clone, Homo sapiens(human) -> XP_011508360.1 Homo sapiens annexin A9 (ANXA9), transcript variant X1, mRNA.

Price & Availability↑

CloneID	OHu61750
Clone ID Related Accession (Same CDS sequence)	XM_011510058.2 , XM_011510058.3
Accession Version	XM_011510058.2	Documents for ORF clone product in default vector
Sequence Information	ORF Nucleotide Sequence (Length: 915bp) 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	2016-06-05
Organism	Homo sapiens(human)
Product	annexin A9 isoform X1
Comment	Comment: MODEL REFSEQ: This record is predicted by automated computational analysis. This record is derived from a genomic sequence (NC_000001.11) annotated using gene prediction method: Gnomon, supported by EST evidence. Also see: Documentation of NCBI's Annotation Process On Jun 6, 2016 this sequence version replaced XM_011510058.1. ##Genome-Annotation-Data-START## Annotation Provider :: NCBI Annotation Status :: Full annotation Annotation Version :: Homo sapiens Annotation Release 108 Annotation Pipeline :: NCBI eukaryotic genome annotation pipeline Annotation Software Version :: 7.0 Annotation Method :: Best-placed RefSeq; Gnomon Features Annotated :: Gene; mRNA; CDS; ncRNA ##Genome-Annotation-Data-END##

ATGTCTGTGA CTGGCGGGAA GATGGCACCG TCCCTCACCC AGGAGATCCT CAGCCACCTG 
GGCCTGGCCA GCAAGACTGC AGCGTGGGGG ACCCTGGGCA CCCTCAGGAC CTTCTTGAAC 
TTCAGCGTGG ACAAGGATGC GCAGAGGCTA CTGAGGGCCA TTACTGGCCA AGGCGTGGAC 
CGCAGTGCCA TTGTGGACGT GCTGACCAAC CGGAGCAGAG AGCAAAGGCA GCTCATCTCA 
CGAAACTTCC AGGAGCGCAC CCAACAGGAC CTGATGAAGT CTCTACAGGC AGCACTTTCC 
GGCAACCTGG AGAGGATTGT GATGGCTCTG CTGCAGCCCA CAGCCCAGTT TGACGCCCAG 
GAATTGAGGA CAGCTCTGAA GGCCTCAGAT TCTGCTGTGG ACGTGGCCAT TGAAATTCTT 
GCCACTCGAA CCCCACCCCA GCTGCAGGAG TGCCTGGCAG TCTACAAACA CAATTTCCAG 
GTGGAGGCTG TGGATGACAT CACATCTGAG ACCAGTGGCA TCTTGCAGGA CCTGCTGTTG 
GCCCTGGCCA AGGGGGGCCG TGACAGCTAC TCTGGAATCA TTGACTATAA TCTGGCAGAA 
CAAGATGTCC AGGCACTGCA GCGGGCAGAA GGACCTAGCA GAGAGGAAAC ATGGGTCCCA 
GTCTTCACCC AGCGAAATCC TGAACACCTC ATCCGAGTGT TTGATCAGTA CCAGCGGAGC 
ACTGGGCAAG AGCTGGAGGA GGCTGTCCAG AACCGTTTCC ATGGAGATGC TCAGGTGGCT 
CTGCTCGGCC TAGCTTCGGT GATCAAGAAC ACACCGCTGT ACTTTGCTGA CAAACTTCAT 
CAAGCCCTCC AGGATGCAGT GAAAGGGGAT TGCCAGTCAG CCCTCCTGGC CTTGTGCAGG 
GCTGAAGACA TGTGA

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

RefSeq	XP_011508360.1
CDS	190..1104
Translation	MSVTGGKMAPSLTQEILSHLGLASKTAAWGTLGTLRTFLNFSVDKDAQRLLRAITGQGVDRSAIVDVLTNRSREQRQLISRNFQERTQQDLMKSLQAALSGNLERIVMALLQPTAQFDAQELRTALKASDSAVDVAIEILATRTPPQLQECLAVYKHNFQVEAVDDITSETSGILQDLLLALAKGGRDSYSGIIDYNLAEQDVQALQRAEGPSREETWVPVFTQRNPEHLIRVFDQYQRSTGQELEEAVQNRFHGDAQVALLGLASVIKNTPLYFADKLHQALQDAVKGDCQSALLALCRAEDM

Target ORF information:

RefSeq Version	XM_011510058.2
Organism	Homo sapiens(human)
Definition	Homo sapiens annexin A9 (ANXA9), transcript variant X1, mRNA.

Target ORF information:

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

XM_011510058.2

ORF Insert Sequence:

ATGTCTGTGA CTGGCGGGAA GATGGCACCG TCCCTCACCC AGGAGATCCT CAGCCACCTG 
GGCCTGGCCA GCAAGACTGC AGCGTGGGGG ACCCTGGGCA CCCTCAGGAC CTTCTTGAAC 
TTCAGCGTGG ACAAGGATGC GCAGAGGCTA CTGAGGGCCA TTACTGGCCA AGGCGTGGAC 
CGCAGTGCCA TTGTGGACGT GCTGACCAAC CGGAGCAGAG AGCAAAGGCA GCTCATCTCA 
CGAAACTTCC AGGAGCGCAC CCAACAGGAC CTGATGAAGT CTCTACAGGC AGCACTTTCC 
GGCAACCTGG AGAGGATTGT GATGGCTCTG CTGCAGCCCA CAGCCCAGTT TGACGCCCAG 
GAATTGAGGA CAGCTCTGAA GGCCTCAGAT TCTGCTGTGG ACGTGGCCAT TGAAATTCTT 
GCCACTCGAA CCCCACCCCA GCTGCAGGAG TGCCTGGCAG TCTACAAACA CAATTTCCAG 
GTGGAGGCTG TGGATGACAT CACATCTGAG ACCAGTGGCA TCTTGCAGGA CCTGCTGTTG 
GCCCTGGCCA AGGGGGGCCG TGACAGCTAC TCTGGAATCA TTGACTATAA TCTGGCAGAA 
CAAGATGTCC AGGCACTGCA GCGGGCAGAA GGACCTAGCA GAGAGGAAAC ATGGGTCCCA 
GTCTTCACCC AGCGAAATCC TGAACACCTC ATCCGAGTGT TTGATCAGTA CCAGCGGAGC 
ACTGGGCAAG AGCTGGAGGA GGCTGTCCAG AACCGTTTCC ATGGAGATGC TCAGGTGGCT 
CTGCTCGGCC TAGCTTCGGT GATCAAGAAC ACACCGCTGT ACTTTGCTGA CAAACTTCAT 
CAAGCCCTCC AGGATGCAGT GAAAGGGGAT TGCCAGTCAG CCCTCCTGGC CTTGTGCAGG 
GCTGAAGACA TGTGA

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

ANXA9 ( XM_011510058.3 ) cDNA ORF clone, Homo sapiens(human) -> XP_011508360.1 Homo sapiens annexin A9 (ANXA9), transcript variant X1, mRNA.

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CloneID	OHu61750
Clone ID Related Accession (Same CDS sequence)	XM_011510058.2 , XM_011510058.3
Accession Version	XM_011510058.3 Latest version!	Documents for ORF clone product in default vector
Sequence Information	ORF Nucleotide Sequence (Length: 915bp) 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	annexin A9 isoform X1
Comment	Comment: MODEL REFSEQ: This record is predicted by automated computational analysis. This record is derived from a genomic sequence (NC_000001.11) annotated using gene prediction method: Gnomon, supported by EST evidence. Also see: Documentation of NCBI's Annotation Process On Mar 26, 2018 this sequence version replaced XM_011510058.2. ##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##

ATGTCTGTGA CTGGCGGGAA GATGGCACCG TCCCTCACCC AGGAGATCCT CAGCCACCTG 
GGCCTGGCCA GCAAGACTGC AGCGTGGGGG ACCCTGGGCA CCCTCAGGAC CTTCTTGAAC 
TTCAGCGTGG ACAAGGATGC GCAGAGGCTA CTGAGGGCCA TTACTGGCCA AGGCGTGGAC 
CGCAGTGCCA TTGTGGACGT GCTGACCAAC CGGAGCAGAG AGCAAAGGCA GCTCATCTCA 
CGAAACTTCC AGGAGCGCAC CCAACAGGAC CTGATGAAGT CTCTACAGGC AGCACTTTCC 
GGCAACCTGG AGAGGATTGT GATGGCTCTG CTGCAGCCCA CAGCCCAGTT TGACGCCCAG 
GAATTGAGGA CAGCTCTGAA GGCCTCAGAT TCTGCTGTGG ACGTGGCCAT TGAAATTCTT 
GCCACTCGAA CCCCACCCCA GCTGCAGGAG TGCCTGGCAG TCTACAAACA CAATTTCCAG 
GTGGAGGCTG TGGATGACAT CACATCTGAG ACCAGTGGCA TCTTGCAGGA CCTGCTGTTG 
GCCCTGGCCA AGGGGGGCCG TGACAGCTAC TCTGGAATCA TTGACTATAA TCTGGCAGAA 
CAAGATGTCC AGGCACTGCA GCGGGCAGAA GGACCTAGCA GAGAGGAAAC ATGGGTCCCA 
GTCTTCACCC AGCGAAATCC TGAACACCTC ATCCGAGTGT TTGATCAGTA CCAGCGGAGC 
ACTGGGCAAG AGCTGGAGGA GGCTGTCCAG AACCGTTTCC ATGGAGATGC TCAGGTGGCT 
CTGCTCGGCC TAGCTTCGGT GATCAAGAAC ACACCGCTGT ACTTTGCTGA CAAACTTCAT 
CAAGCCCTCC AGGATGCAGT GAAAGGGGAT TGCCAGTCAG CCCTCCTGGC CTTGTGCAGG 
GCTGAAGACA TGTGA

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

RefSeq	XP_011508360.1
CDS	208..1122
Translation	MSVTGGKMAPSLTQEILSHLGLASKTAAWGTLGTLRTFLNFSVDKDAQRLLRAITGQGVDRSAIVDVLTNRSREQRQLISRNFQERTQQDLMKSLQAALSGNLERIVMALLQPTAQFDAQELRTALKASDSAVDVAIEILATRTPPQLQECLAVYKHNFQVEAVDDITSETSGILQDLLLALAKGGRDSYSGIIDYNLAEQDVQALQRAEGPSREETWVPVFTQRNPEHLIRVFDQYQRSTGQELEEAVQNRFHGDAQVALLGLASVIKNTPLYFADKLHQALQDAVKGDCQSALLALCRAEDM

Target ORF information:

RefSeq Version	XM_011510058.3
Organism	Homo sapiens(human)
Definition	Homo sapiens annexin A9 (ANXA9), transcript variant X1, mRNA.

Target ORF information:

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

XM_011510058.3

ORF Insert Sequence:

ATGTCTGTGA CTGGCGGGAA GATGGCACCG TCCCTCACCC AGGAGATCCT CAGCCACCTG 
GGCCTGGCCA GCAAGACTGC AGCGTGGGGG ACCCTGGGCA CCCTCAGGAC CTTCTTGAAC 
TTCAGCGTGG ACAAGGATGC GCAGAGGCTA CTGAGGGCCA TTACTGGCCA AGGCGTGGAC 
CGCAGTGCCA TTGTGGACGT GCTGACCAAC CGGAGCAGAG AGCAAAGGCA GCTCATCTCA 
CGAAACTTCC AGGAGCGCAC CCAACAGGAC CTGATGAAGT CTCTACAGGC AGCACTTTCC 
GGCAACCTGG AGAGGATTGT GATGGCTCTG CTGCAGCCCA CAGCCCAGTT TGACGCCCAG 
GAATTGAGGA CAGCTCTGAA GGCCTCAGAT TCTGCTGTGG ACGTGGCCAT TGAAATTCTT 
GCCACTCGAA CCCCACCCCA GCTGCAGGAG TGCCTGGCAG TCTACAAACA CAATTTCCAG 
GTGGAGGCTG TGGATGACAT CACATCTGAG ACCAGTGGCA TCTTGCAGGA CCTGCTGTTG 
GCCCTGGCCA AGGGGGGCCG TGACAGCTAC TCTGGAATCA TTGACTATAA TCTGGCAGAA 
CAAGATGTCC AGGCACTGCA GCGGGCAGAA GGACCTAGCA GAGAGGAAAC ATGGGTCCCA 
GTCTTCACCC AGCGAAATCC TGAACACCTC ATCCGAGTGT TTGATCAGTA CCAGCGGAGC 
ACTGGGCAAG AGCTGGAGGA GGCTGTCCAG AACCGTTTCC ATGGAGATGC TCAGGTGGCT 
CTGCTCGGCC TAGCTTCGGT GATCAAGAAC ACACCGCTGT ACTTTGCTGA CAAACTTCAT 
CAAGCCCTCC AGGATGCAGT GAAAGGGGAT TGCCAGTCAG CCCTCCTGGC CTTGTGCAGG 
GCTGAAGACA TGTGA

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

PubMed

Discovery and refinement of loci associated with lipid levels.
Nature genetics45(11)1274-1283(2013 Nov)
Willer CJ,Schmidt EM,Sengupta S,Peloso GM,Gustafsson S,Kanoni S,Ganna A,Chen J,Buchkovich ML,Mora S,Beckmann JS,Bragg-Gresham JL,Chang HY,Demirkan A,Den Hertog HM,Do R,Donnelly LA,Ehret GB,Esko T,Feitosa MF,Ferreira T,Fischer K,Fontanillas P,Fraser RM,Freitag DF,Gurdasani D,Heikkil? K,Hypp?nen E,Isaacs A,Jackson AU,Johansson ?,Johnson T,Kaakinen M,Kettunen J,Kleber ME,Li X,Luan J,Lyytik?inen LP,Magnusson PKE,Mangino M,Mihailov E,Montasser ME,M?ller-Nurasyid M,Nolte IM,O'Connell JR,Palmer CD,Perola M,Petersen AK,Sanna S,Saxena R,Service SK,Shah S,Shungin D,Sidore C,Song C,Strawbridge RJ,Surakka I,Tanaka T,Teslovich TM,Thorleifsson G,Van den Herik EG,Voight BF,Volcik KA,Waite LL,Wong A,Wu Y,Zhang W,Absher D,Asiki G,Barroso I,Been LF,Bolton JL,Bonnycastle LL,Brambilla P,Burnett MS,Cesana G,Dimitriou M,Doney ASF,D?ring A,Elliott P,Epstein SE,Ingi Eyjolfsson G,Gigante B,Goodarzi MO,Grallert H,Gravito ML,Groves CJ,Hallmans G,Hartikainen AL,Hayward C,Hernandez D,Hicks AA,Holm H,Hung YJ,Illig T,Jones MR,Kaleebu P,Kastelein JJP,Khaw KT,Kim E,Klopp N,Komulainen P,Kumari M,Langenberg C,Lehtim?ki T,Lin SY,Lindstr?m J,Loos RJF,Mach F,McArdle WL,Meisinger C,Mitchell BD,M?ller G,Nagaraja R,Narisu N,Nieminen TVM,Nsubuga RN,Olafsson I,Ong KK,Palotie A,Papamarkou T,Pomilla C,Pouta A,Rader DJ,Reilly MP,Ridker PM,Rivadeneira F,Rudan I,Ruokonen A,Samani N,Scharnagl H,Seeley J,Silander K,Stan??kov? A,Stirrups K,Swift AJ,Tiret L,Uitterlinden AG,van Pelt LJ,Vedantam S,Wainwright N,Wijmenga C,Wild SH,Willemsen G,Wilsgaard T,Wilson JF,Young EH,Zhao JH,Adair LS,Arveiler D,Assimes TL,Bandinelli S,Bennett F,Bochud M,Boehm BO,Boomsma DI,Borecki IB,Bornstein SR,Bovet P,Burnier M,Campbell H,Chakravarti A,Chambers JC,Chen YI,Collins FS,Cooper RS,Danesh J,Dedoussis G,de Faire U,Feranil AB,Ferri?res J,Ferrucci L,Freimer NB,Gieger C,Groop LC,Gudnason V,Gyllensten U,Hamsten A,Harris TB,Hingorani A,Hirschhorn JN,Hofman A,Hovingh GK,Hsiung CA,Humphries SE,Hunt SC,Hveem K,Iribarren C,J?rvelin MR,Jula A,K?h?nen M,Kaprio J,Kes?niemi A,Kivimaki M,Kooner JS,Koudstaal PJ,Krauss RM,Kuh D,Kuusisto J,Kyvik KO,Laakso M,Lakka TA,Lind L,Lindgren CM,Martin NG,M?rz W,McCarthy MI,McKenzie CA,Meneton P,Metspalu A,Moilanen L,Morris AD,Munroe PB,Nj?lstad I,Pedersen NL,Power C,Pramstaller PP,Price JF,Psaty BM,Quertermous T,Rauramaa R,Saleheen D,Salomaa V,Sanghera DK,Saramies J,Schwarz PEH,Sheu WH,Shuldiner AR,Siegbahn A,Spector TD,Stefansson K,Strachan DP,Tayo BO,Tremoli E,Tuomilehto J,Uusitupa M,van Duijn CM,Vollenweider P,Wallentin L,Wareham NJ,Whitfield JB,Wolffenbuttel BHR,Ordovas JM,Boerwinkle E,Palmer CNA,Thorsteinsdottir U,Chasman DI,Rotter JI,Franks PW,Ripatti S,Cupples LA,Sandhu MS,Rich SS,Boehnke M,Deloukas P,Kathiresan S,Mohlke KL,Ingelsson E,Abecasis GR,

Genome-wide association study identifies genetic risk underlying primary rhegmatogenous retinal detachment.
Human molecular genetics22(15)3174-85(2013 Aug)
Kirin M,Chandra A,Charteris DG,Hayward C,Campbell S,Celap I,Bencic G,Vatavuk Z,Kirac I,Richards AJ,Tenesa A,Snead MP,Fleck BW,Singh J,Harsum S,Maclaren RE,den Hollander AI,Dunlop MG,Hoyng CB,Wright AF,Campbell H,Vitart V,Mitry D

Annexin A9 is a periplakin interacting partner in membrane-targeted cytoskeletal linker protein complexes.
FEBS letters586(19)3090-6(2012 Sep)
Boczonadi V,M??tt? A

Genome-wide association study identifies a new melanoma susceptibility locus at 1q21.3.
Nature genetics43(11)1114-8(2011 Oct)
Macgregor S,Montgomery GW,Liu JZ,Zhao ZZ,Henders AK,Stark M,Schmid H,Holland EA,Duffy DL,Zhang M,Painter JN,Nyholt DR,Maskiell JA,Jetann J,Ferguson M,Cust AE,Jenkins MA,Whiteman DC,Olsson H,Puig S,Bianchi-Scarr? G,Hansson J,Demenais F,Landi MT,D?bniak T,Mackie R,Azizi E,Bressac-de Paillerets B,Goldstein AM,Kanetsky PA,Gruis NA,Elder DE,Newton-Bishop JA,Bishop DT,Iles MM,Helsing P,Amos CI,Wei Q,Wang LE,Lee JE,Qureshi AA,Kefford RF,Giles GG,Armstrong BK,Aitken JF,Han J,Hopper JL,Trent JM,Brown KM,Martin NG,Mann GJ,Hayward NK

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ANXA9 cDNA ORF clone, Homo sapiens(human)

Gene

Clones

gRNAs

Related articles in PubMed

Target ORF information:

Target ORF information:

ORF Insert Sequence:

Target ORF information:

Target ORF information:

ORF Insert Sequence:

Target ORF information:

Target ORF information:

ORF Insert Sequence:

Target ORF information:

Target ORF information:

ORF Insert Sequence:

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