GPR172B (SLC52A1) (NM_017986) Human 3' UTR Clone

CAT#: SC204965

3' UTR clone of G protein-coupled receptor 172B (GPR172B) transcript variant 2 for miRNA target validation



Need custom modification / cloning service?
Get a free quote

CNY 4,845.00


货期*
3周

规格
    • 10 ug

Product images

经常一起买 (2)
Firefly luciferase assay kit, 150 assays
    • 1 kit

CNY 1,520.00


DH5α Chemically Competent Cells (≥10^8 cfu/μg of pUC19 DNA)
    • 5 x 200 ul

CNY 1,280.00

Specifications

Product Data
Product Name GPR172B (SLC52A1) (NM_017986) Human 3' UTR Clone
Vector pMirTarget
Synonyms GPCR42; GPR172B; hRFT1; huPAR-2; PAR2; RBFVD; RFT1; RFVT1
ACCN NM_017986
Insert Size 385 bp
Sequence Data
>SC204965 3’UTR clone of NM_017986
The sequence shown below is from the reference sequence of NM_017986. 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_017986.4
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
*Delivery time may vary from web posted schedule. Occasional delays may occur due to unforeseen complexities in the preparation of your product. International customers may expect an additional 1-2 weeks in shipping.

Documents

Customer Reviews 
Loading...