NBPF15 (NM_173638) Human 3' UTR Clone
CAT#: SC215712
3' UTR clone of neuroblastoma breakpoint family member 15 (NBPF15) for miRNA target validation
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CNY 5795.00
货期*
3周
规格
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Specifications
Product Data | |
Product Name | NBPF15 (NM_173638) Human 3' UTR Clone |
Vector | pMirTarget |
Synonyms | AB14; AG3; NBPF16 |
ACCN | NM_173638 |
Insert Size | 1653 bp |
Sequence Data |
>SC215712 3’UTR clone of NM_173638
The sequence shown below is from the reference sequence of NM_173638. The complete sequence of this clone may contain minor differences, such as SNPs. Blue=Stop Codon Red=Cloning site GGCAAGTTGGACGCCCGCAAGATCCGCGAGATTCTCATTAAGGCCAAGAAGGGCGGAAAGATCGCCGTG TAACAATTGGCAGAGCTCAGAATTCAAGCGATCGCC TTCCAGATGGGAGTCATATTCCCACAATAAGCAGCTCTTACTAAGCCGAGAGATGTCATTCCTGCAGGC AGGACCTATAGGCACGAGAAGATTTGAATGAAAGTACAGTTCCATTTGGAAGCCCAGACATAGGATGGG TCAGTGAGCATGGCTCTATTCCTATTCTCAAACCATGCCATTGGCAACCTGTGCTCAATCTGAAGACAA TGGACCCATGTTAGGTGTGACACGTTCACATAACTGTGCAGAACATGCCGGGAGTGATCAGTCAGACAT TTTAATTTGAACCACGTATCTCTGGGTAGCTACAAAATTCCTCAGGGATTTCATTTTGCAGGCATGTCT CTGAGCTTCTATACCTGCTCAAGGTCATTGTCATCTTTGTGTTTAGCTCATCCAAAGGTGTTACCCTGG TTTCAATGAACCTAACCTCATTCTTTGTGTCTTCAGTGTTGGCTTGTTTTAGCTGATCCATCTGTAACA CAGGAGGGATCCTTGGCTGAGGATTGTATTTCAGAACCACCAACTGCTCTTGACAATTGTTAACCCGCT AGGCTCCTTTGGTTAGAGAAGCCACAGTCCTTCAGCCTCCAATTGGTGTCAGTACTTAGGAAGACCACA GCTAGATGGACAAACAGCATTGGGAGGCCTTAGCCCTGCTCCTCTCAATTCCATCCTGTAGAGAACAGG AGTCAGGAGCCGCTGGCAGGAGACAGCATGTCACCCAGGACTCTGCCGGTGCAGAATATGAACAATGCC ATGTTCTTGCAGAAAACACTTAGCCTGAGTTTCATAGGAGGTAATCACCAGACAACTGCAGAATGTAGA ACACTGAGCAGGACAACTGACCTGTCTCCTTCACATAGTCCATATCACCACAAATCACACAACAAAAAG GAGAAGAGATATTTTGGGTTCAAAAAAAGTAAAAAGATAATGTAGCTGCATTTCTTTAGTTATTTTGAA CCCCAAATATTTCCTCATCTTTTTGTTGTTGTCATGGATGGTGGTGACATGGACTTGTTTATAGAGGAC AGGTCAGCTGTCTGGCTCAATGATCTACATTCTGAAGTTGTCTGAAAATGTCTTCATGATTAAATTCAG CCTAAACATTTTGCCGGGAACACTGCAGAGACAATGCTGTGAGTTTCCAACCTCAGCCCATCTGCGGGC AGAGAAGGTCTAGTTTGTCCATCACCATTATGATATCAGGACTGGTTACTTGGTTAAGGAGGGGTCTAG GAGATCTGTCCCTTTTAGAGACACCTTACTTATAATGAAGTACTTGGGAAAGCGGTTTTCAAGAGTATA AATATCCTGTATTCTAATGATCATCCTCTAAACATTTTATCATTTATTAATCCTCCCTGCCTGTGTCTA TTATTATATTCATATCTCTACACTGCAAATTTTGGGTCTCAATTTTTACTGTGCCTTTGTTTTTACTAG TGTCTGCTGTTGCAAAAAGAAGAAAACATTCTCTGCCTGAGTTTTAATTTTTGTCCAAAGTTAATTTTA ATCTATACAATTAAAACCTTTTGCCTATCACTCTGGACTTCTGGATTGTTTTTTACATTCAGTGTTATA ATATTTGATTATGCTGATTGGTTTTGGTGGGTACTGATGCGAATTAATAAAAACATTTCATTTCCA 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_173638.5 |
Synonyms | AB14; AG3; NBPF16 |
Summary | This gene is a member of the neuroblastoma breakpoint family (NBPF) which consists of dozens of recently duplicated genes primarily located in segmental duplications on human chromosome 1. This gene family has experienced its greatest expansion within the human lineage and has expanded, to a lesser extent, among primates in general. Members of this gene family are characterized by tandemly repeated copies of DUF1220 protein domains. Gene copy number variations in the human chromosomal region 1q21.1, where most DUF1220 domains are located, have been implicated in a number of developmental and neurogenetic diseases such as microcephaly, macrocephaly, autism, schizophrenia, cognitive disability, congenital heart disease, neuroblastoma, and congenital kidney and urinary tract anomalies. Altered expression of some gene family members is associated with several types of cancer. This gene family contains numerous pseudogenes. [provided by RefSeq, May 2013] |
Locus ID | 284565 |
MW | 63 |
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