PEX10 (NM_002617) Human 3' UTR Clone
CAT#: SC211560
3' UTR clone of peroxisomal biogenesis factor 10 (PEX10) transcript variant 2 for miRNA target validation
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CNY 4,845.00
货期*
3周
规格
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经常一起买 (2)
Specifications
Product Data | |
Product Name | PEX10 (NM_002617) Human 3' UTR Clone |
Vector | pMirTarget |
Synonyms | NALD; PBD6A; PBD6B; RNF69 |
ACCN | NM_002617 |
Insert Size | 1822 bp |
Sequence Data |
>SC211560 3’UTR clone of NM_002617
The sequence shown below is from the reference sequence of NM_002617. The complete sequence of this clone may contain minor differences, such as SNPs. Blue=Stop Codon Red=Cloning site GGCAAGTTGGACGCCCGCAAGATCCGCGAGATTCTCATTAAGGCCAAGAAGGGCGGAAAGATCGCCGTG TAACAATTGGCAGAGCTCAGAATTCAAGCGATCGCC AAGCTCATCTACCTTCGGCACTACCGCTGAGCCGGCGCCCGGGTGGGCCTGGACACAGATGACCTCTAC GGGAGTCTGAACGCCAAGATTTAGTCTCAGGATTAACCTTGCTTGCACAGAAGTTAGAACACTCTCAGT TTTTTGTCATGTAAGATACTAACCTAGCCACCCTGGGAGAGAACAGAAAGCTGTCCCTGGCTGCGCTTT CTCAGCCCTGGGAGGGGCGCCTGAACCCAGAACATTTCCCTAACCCCAACCTGGTAGGACTCAGCCACT TCTTCAGGAATTTCACTTATTTGGACGGGATTTTAGGTTTCCCTCCCTTCCCCAAACCATACAGTTGAG AAGTAATTCAGAAGTAGGCCAGAAGACACTTTATTCGTTTATATTGTGAGAAAACAGCCCCATCAGGCT TGTGTTAAGGCAATGGACTGAATGAGTGCGTGCTGGGTGGGGTGGGGCACGGAGGCTGGCGGGTTGCTT CAGCCAGTGCAGTGAGAACAGCAGCCCCACGGCCCCATGGGAGGCGGCGCTGCTCTCCCCGAGGGCGGC TGGGCAGAGCACATCCCCCAGGACTTGATGACCACACGGGGCAGAGAGAAACCAACCAAGGCCAGCACC TCCGTCGGAAGCATTTGGCACACACACCTTCAATACACGTCAAGGTCGCTTCCAGTTTTAGAAAACAGA AATCTGCATCTCAGCCTGAGACGCACAGAGAGGTCTCTTCCTGACCCAGACGCACTCACGAGCCAGGTC CTGGGGGTATGGGGGCTGCCAGGGGCGCCCGAGCCCTCTCCTGGGGGGCCTGCTGGGCAGGCGACCTGC TGACCCACGGTCACTGCTGTGTTCAGCCCCTCAGCTCGGCCCCAGCCTATTTCCCGCCTCCATTTGATG TTTCCAGGTTTTCAAAACTGCATTTAACCTGCGCCAGAGAGTTCACCGTAGGCATCTTTAATAAACTAA CTCCAGCAAAATGTGGGTACGTTACTAACACAAGATGGAACTTGAGATTTCCTGAAGCGCAGTGTTAAA ATGCCTCGAGGGCGTGTGCCACATTTCCCTGCTGACGTAAAACACCTGGCCAGCAGGACCGGCTTCCGG CAAAGACCCGCGCAAACCATGTCTTGCTGTTTGACTTACTTAGGAATGAGGATGACCCTGTATTCCTGG GTTAGTCAAGGTCAGCTTGCCAGAGACGGAGGAGGGCGGGGGGGCCGTGACCCTCTAGACTGGGAGGAC CACCAGGAGAGGCACTGGGGGCTGCGGCCGGGTGGGCAGATGCCGCCGTGGCTCCATCCATCAGCACCC AGTCCTTTGCTTCACTGTGCTCTGGCCAAGCGCGTGCGACTTCCTGTCACACCTTAGGCCTGAGCGCTT ATTAAGAAAACAGTATGAAAAATGACAAACACTCCTGTCCACAGTCTGAGAATCCCAAGTGTCTCAACA CGGTACCAGAAGTACCACCTGGGAGCAGCACTGGCTATCTTGGGTCAGGGACACACAAGCTTGAACGTG GCCTCTTAGAGGAGCTCGATGTCAGATATGTAAACACTGGTACAAGAAAATCCAGACACTAAGCATTCA CCGTGTCAATTCTGAGACAGGAAACACCGCCCAGAGTGAGGAGCCTGCGCAGCCCGGGGCCCAGGAGGA GAGGCCTTCACTCGCATGTCAGTGTCTCATCTGGGACCACAGCTGTGATGTTCTGCTGTGCAATATGGG TCACCTTTCGAAAAGGCCAAACAAAAGGTGGGCTTTCCTGTGTCCAGCGACTGCCATGTTTTAGGTAAA GACTTTAGTAAAGGTGGAGGTAAAATCA ACGCGTAAGCGGCCGCGGCATCTAGATTCGAAGAAAATGACCGACCAAGCGACGCCCAACCTGCCATCA CGAGATTTCGATTCCACCGCCGCCTTCTATGAAAGG |
Restriction Sites | SgfI-MluI |
OTI Disclaimer | Our molecular clone sequence data has been matched to the sequence identifier above as a point of reference. Note that the complete sequence of this clone is largely the same as the reference sequence but may contain minor differences , e.g., single nucleotide polymorphisms (SNPs). |
Reference Data | |
RefSeq | NM_002617.4 |
Synonyms | NALD; PBD6A; PBD6B; RNF69 |
Summary | This gene encodes a protein involved in import of peroxisomal matrix proteins. This protein localizes to the peroxisomal membrane. Mutations in this gene result in phenotypes within the Zellweger spectrum of peroxisomal biogenesis disorders, ranging from neonatal adrenoleukodystrophy to Zellweger syndrome. Alternative splicing results in two transcript variants encoding different isoforms. [provided by RefSeq, Jul 2008] |
Locus ID | 5192 |
MW | 66.5 |
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