VGCNL1 (NALCN) (NM_052867) Human 3' UTR Clone

CAT#: SC215043

3' UTR clone of sodium leak channel non-selective (NALCN) for miRNA target validation



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CNY 5,795.00


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 VGCNL1 (NALCN) (NM_052867) Human 3' UTR Clone
Vector pMirTarget
Synonyms bA430M15.1; CanIon; CLIFAHDD; IHPRF; IHPRF1; INNFD; VGCNL1
ACCN NM_052867
Insert Size 1549 bp
Sequence Data
>SC215043 3’UTR clone of NM_052867
The sequence shown below is from the reference sequence of NM_052867. The complete sequence of this clone may contain minor differences, such as SNPs.
Blue=Stop Codon Red=Cloning site

GGCAAGTTGGACGCCCGCAAGATCCGCGAGATTCTCATTAAGGCCAAGAAGGGCGGAAAGATCGCCGTG
TAACAATTGGCAGAGCTCAGAATTCAAGCGATCGCC
GAAAGTGGGGATGACCTTCTGGATATTTAGGTGGATGTCAATGTAGATGAATTTCTAGTGGTGGAAACC
GTTTTCTAATAATGTCCTTGATTGTCCAGTGAGCAATCTGTAATTGATCTATAACTGAATTCCAGCTTG
TCACAAGATGTTTATAAATTGATTTTCATCCTGCCACAGAAAGGCATAAGCTGCATGTATGATGGGTTA
CTATCAATCATTGCTCAAAAAAATTTTTGTATAATGACAGTACTGATAATATTAGAAATGATACCGCAA
GCAAATGTATATCACTTAAAAATGTCATATATTCTGTCTGCGTAAACTAAGGTATATATTCATATGTGC
TCTAATGCAGTATTATCACCGCCCCGCAAAAGAGTGCTAAGCCCAAAGTGGCTGATATTTAGGGTACAG
GGGTTATAGCTTTAGTTCACATCTTTCCCATTTCCACTAGAAATATTTCTCTTGAGAGAATTTATTATT
TATGATTGATCTGAAAAGGTCAGCACTGAACTTATGCTAAAATGATAGTAGTTTTACAAACTACAGATT
CTGAATTTTAAAAAGTATCTTCTTTTTCTCGTGTTATATTTTTAAATATACACAAGACATTTGGTGACC
AGAACAAGTTGATTTCTGTCCTCAGTTATGTTAATGAAACTGTTGCCTCCTTCTAAGAAAATTGTGTGT
GCAAGCACCAGGCAAAGAAATGGACTCAGGATGCTTAGCGGTTTAAAACAAACCTGTAGATAAATCACT
TGAGTGACATAGTTGCGCAAAGATGTTAAGTTTCTTAAGAAACCTTTTAATAACTGAGTTTAGCAAAAA
GAATAAAACTATATAGCTCAATTTATTTAAAAAAATCTTTGCATGTGTGATGTTATCATTGGCTTCATT
TCTTACCCAAGGTATGTCTGTTTTGCCATAAATCAGCAGAGTCATTTCATTCTGGGTGATCCTAACACA
CCATTGCTACGTTAGATTTGAAATGACATCTCTGTTAAAAGAATCTTCTATGGAAATAATGGTGCCCTG
CAAAATCTTCCTTTGAACTCACAGGTTAGGGATCACACAACTTACTTAATCGTTTTTTGTTTTTGTTTT
TTTTCCTTATATGTCAATGGCCCATGTCCTCCGGGAAAATTAGAAAAGCAAAATGATTACAAAGTGCTG
TTAGATTTCTTGTGCTGGGCCAGCCAAGTAGAAGTGGACTTGACTTGGACCTTTAACTATTTTATTACA
GATTGGACATTTGCTGTTCAGATGTTTTTTAACAGAGGGATTATCTCAGAATCCTGTGACCTCCAGGTT
GTTTTATAATCTATTTTTCTCTATTTAACATTCCTCAGATAGATAGGCAAATAGGACATTCCTTCTGTG
TCACAGAAGTATCGTGGTAGTGGCAGTCTACAGTTTATATGATTCATTGTAACTATGAGATAAAGAACA
ACCAGTCATGTGGCCAAAAGGATTAGATTTGATTTGATGTTCACTTGGAGTTTACTTTTTGTACATACA
AGATAAAATAAATATTGGATTTGTAAAATAA
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_052867.4
Synonyms bA430M15.1; CanIon; CLIFAHDD; IHPRF; IHPRF1; INNFD; VGCNL1
Summary This gene encodes a voltage-independent, nonselective cation channel which belongs to a family of voltage-gated sodium and calcium channels that regulates the resting membrane potential and excitability of neurons. This family is expressed throughout the nervous system and conducts a persistent sodium leak current that contributes to tonic neuronal excitability. The encoded protein forms a channelosome complex that includes G-protein-coupled receptors, UNC-79, UNC-80, NCA localization factor-1, and src family tyrosine kinases. Naturally occurring mutations in this gene are associated with infantile neuroaxonal dystrophy, infantile hypotonia with psychomotor retardation and characteristic facies (IHPRF) syndrome, and congenital contractures of the limbs and face with hypotonia and developmental delay (CLIFAHDD) syndrome. A knockout of the orthologous gene in mice results in paralysis with a severely disrupted respiratory rhythm, and lethality within 24 hours after birth. [provided by RefSeq, Apr 2017]
Locus ID 259232
MW 60.2
*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.

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