GPR172B (SLC52A1) (NM_001104577) Human 3' UTR Clone
CAT#: SC204966
3' UTR clone of G protein-coupled receptor 172B (GPR172B) transcript variant 1 for miRNA target validation
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CNY 4,845.00
货期*
3周
规格
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Specifications
Product Data | |
Product Name | GPR172B (SLC52A1) (NM_001104577) Human 3' UTR Clone |
Vector | pMirTarget |
Synonyms | GPCR42; GPR172B; hRFT1; huPAR-2; PAR2; RBFVD; RFT1; RFVT1 |
ACCN | NM_001104577 |
Insert Size | 385 bp |
Sequence Data |
>SC204966 3’UTR clone of NM_001104577
The sequence shown below is from the reference sequence of NM_001104577. The complete sequence of this clone may contain minor differences, such as SNPs. Blue=Stop Codon Red=Cloning site GGCAAGTTGGACGCCCGCAAGATCCGCGAGATTCTCATTAAGGCCAAGAAGGGCGGAAAGATCGCCGTG TAACAATTGGCAGAGCTCAGAATTCAAGCGATCGCC AAGGACTGTGTAGACCCCTGTGGCCCCTGAGCCTGGGCAGGTGGGGACCCAACTCCACCCCACCTGTCT TCATCGTGAGGCTGCCACAGTGCCTGACTACTTGTGGCCCAGGCAGGCTTCCCCCAACACAGGAACGCT CATGGACACCTGCACACTCCACAGAAGACGTTGGCATGTGAGGCCAGGGTGGGCACCAAAGACCAGGCC CAGAGCCAGGGGACAGGTTGGGGCTGTGGGCTTGGACCCAGGGCCTGAGACCTTTGTGGGATTTGTGCA ATAAAGTGTTTTTATTTAAAACCAAAAACAAAAACAAAAGCCTAATGAAAACCTTATAAGAAATATATA ATGAAATCAGGAAACTGGATTAAATAATTTTTCATACATA 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_001104577.2 |
Synonyms | GPCR42; GPR172B; hRFT1; huPAR-2; PAR2; RBFVD; RFT1; RFVT1 |
Summary | Biological redox reactions require electron donors and acceptor. Vitamin B2 is the source for the flavin in flavin adenine dinucleotide (FAD) and flavin mononucleotide (FMN) which are common redox reagents. This gene encodes a member of the riboflavin (vitamin B2) transporter family. Haploinsufficiency of this protein can cause maternal riboflavin deficiency. Multiple alternatively spliced variants, encoding the same protein, have been identified. [provided by RefSeq, Jan 2013] |
Locus ID | 55065 |
MW | 13.9 |
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