GGCX (NM_001142269) Human 3' UTR Clone

CAT#: SC210578

3' UTR clone of gamma-glutamyl carboxylase (GGCX) transcript variant 2 for miRNA target validation



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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 GGCX (NM_001142269) Human 3' UTR Clone
Vector pMirTarget
Synonyms VKCFD1
ACCN NM_001142269
Insert Size 2000 bp
Sequence Data
>SC210578 3’UTR clone of NM_001142269
The sequence shown below is from the reference sequence of NM_001142269. The complete sequence of this clone may contain minor differences, such as SNPs.
Blue=Stop Codon Red=Cloning site

GGCAAGTTGGACGCCCGCAAGATCCGCGAGATTCTCATTAAGGCCAAGAAGGGCGGAAAGATCGCCGTG
TAACAATTGGCAGAGCTCAGAATTCAAGCGATCGCC
AATCCTGATCCTGTCCACTCAGAGTTCTGAAGGGGGCCAGATGTTGGGTGCAGATGTAGAAGCAGCCAG
TCACAGACCCATTCTATGCAATGGACATTTATTTGAAAAAAATTCTCAAAAGTTTTTTTTTTTTTTTTG
GGGGGGCGGGGTTCTAAAGCTGTTTTTAACTCCGAGATTACAACTTAGAGGAACCAAGGAAATAAAGCA
AATAAGATTTAACAACCCAAGATTAAGAGGCCAGGAAGAGGTTAGACGCAATGTGAAACTGTCCTCCTA
GGATAAGGTTTAAAGTGGCTTTTTGGGGGCTGGGTGCCGTGGCTCACGCCTGTAATCCCAGCATTTTGG
GAGGCTGAGGTGGGCAGATCACTTGAGGCCAGGAGTTCGAGACCAGCCTGGCCAACATGGCAAAACCCC
TTCTCTACTAAAAATACAAAAATTAGCCAGACGTGGTGGTGGGTGCCTGTAATCCAACTACCCAGGAGG
CTGAGGCATGAGAATCGCTTGGGCCCAGGAGGTGGAGGTTGCAGTGAGCCGAGATCGAGCCACTGCACT
CCTGGGCAACAGAGCAAGACTTCGTCTCAAAATAAATAAATAAAGTGGCTCTTGGGGAAAAGCAATTTA
ATGTACCACGATGAATAGCTAACTGTTCCCAAGTGTTTGCTATGTGCAACACACCGCGTGAGCAGTGTT
ACCTGCATTATTACATTAGGCTGAGAGGTAAAATAATTTGCCCGAAGACATACAGCTAGTGACGAATGG
ACTGATGGTTTGAACTTAACGTCTATTTGACTTAAGGTCCTGCACCCTGCCACTTGTAATTTTCAGAAT
CACTGATAATCTGAAATAATGCAGCTTAAAACATGTTTTCTTAATTAAAAGTATAATTGGATGGTGGTC
AGGTTGTAAATGCACACAAAGTAATTTATCTTCATTGCAATTTTGGTTCCTTCTTTGTTCCTATTATCT
ATATACACCCAGTGTTTCACTAGCAGTTATGAGAGCAGTCAGAATAGCAGCATCAAAGTTAAATAAGGA
AATCTAGATGATTGCTAGATTTTCTCTAAAAATAAGCTTAGTATTTGGTATTATTCTAGCCTTTGGTGA
GCAGAAGGGGAGGTAAAGTAAGAATTAACTAAATTTAGTAAGGGATTAGGGAATGCTTAGACATTTTGT
AGGTTGGGGTATACAAGGGTAACTCAGGAAGCTCCTCAGTTCAGTGAAAATTCAAAGGGTTGGCACTGA
GCTAGGAAGCGAGAATGCAGGGTTATGAAAAAGGATCCCTGCTTTGGGAGCTCATGGACTTGTAGCAGA
GACCGGTAGTAAATTGGCAGTCTCAGTAACTTCTGTAAATGATTGCATCTCTTTGCAGGCTTCTCTTCC
CATACTCTCCCCCACTCCTCCTTGGACAGTGTTCCGGGGGTTCTTTCCTAAGCAACTGCTTTTTCAGTA
TACATACTTCAGATGATTGTGTCTACTCCAGGATTTCCAACGATGCTAGGTTTCTTTCCTGTGCCCTAG
ACGTATAGGTCTAAGTTCCACCTGGATATCCCACAGGGCTATCAAGCTCAGTTCATCCTAAACAGAACT
TACATTCATCCCCAACTCAGACTTCCTTATTCTTTATTATTGAATGGCAGCTCTGTACCTTAGCCAAGC
TGTTATCTCTAGGTCATCAGCCTTGACTCTTCCTTTTTCCTTGCATTTCTTAAAATTGCCAAGTCCCAT
CAATTTTACCTCCTGGATACCTCTTGAATCTATTTTTTTTTAAAGACAGGGTTTCACTCTATCACCCAG
GCTGGAGTTCAGTGGCACAATCTTGGCTTACTGCAGCCACCACCTCCTGGGTTTAAACGATTCTTCCAC
TTCAGCCTCCCATGTAGCTGGGACTACAGGTGCCCACCACCACGCCCAACTAATTTTTGTATTTTTAGT
AGAGACATGGTTTCCCACATTGGCCAGGCTGGTCTCAAACTCATGACCTTAAGTATCCACCTGCCTTG
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_001142269.4
Synonyms VKCFD1
Summary This gene encodes an integral membrane protein of the rough endoplasmic reticulum that carboxylates glutamate residues of vitamin K-dependent proteins to gamma carboxyl glutamate, a modification that is required for their activity. The vitamin K-dependent protein substrates have a propeptide that binds the enzyme, with carbon dioxide, dioxide, and reduced vitamin K acting as co-substrates. Vitamin K-dependent proteins affect a number of physiologic processes including blood coagulation, prevention of vascular calcification, and inflammation. Allelic variants of this gene have been associated with pseudoxanthoma elasticum-like disorder with associated multiple coagulation factor deficiency. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Aug 2015]
Locus ID 2677
MW 75.8
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