SNRPN (NM_022808) Human Untagged Clone

CAT#: SC112434

SNRPN (untagged)-Human small nuclear ribonucleoprotein polypeptide N (SNRPN), transcript variant 5



  "NM_022808" in other vectors (4)

CNY 2,400.00

CNY 2,950.00


货期*
现货

规格
    • 10 ug

Product images

经常一起买 (4)
TurboFectin Transfection Reagent (1 mL in 1 vial)
    • 1 ml in 1 vial

CNY 4,090.00


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

CNY 1,280.00


Forward sequencing primer VP1.5, Reverse sequencing primer XL39, 100pmoles each
    • 100 pmol

CNY 480.00


Rabbit Polyclonal Anti-SNRPN Antibody
    • 100 ug

CNY 5,808.00

Specifications

Product Data
Type Human Untagged Clone
Tag Tag Free
Synonyms HCERN3; PWCR; PWS; RT-LI; SM-D; sm-N; SMN; SNRNP-N; SNURF-SNRPN
Vector pCMV6-XL5
E. coli Selection Ampicillin (100 ug/mL)
Mammalian Cell Selection None
Sequence Data
>NCBI ORF sequence for NM_022808, the custom clone sequence may differ by one or more nucleotides


ATGACTGTTGGCAAGAGTAGCAAGATGCTGCAGCACATTGACTATAGAATGAGATGTATCCTGCAAGATG
GCCGAATCTTCATTGGCACCTTTAAGGCTTTTGACAAGCATATGAATTTGATCCTCTGTGATTGTGATGA
GTTCAGAAAGATCAAGCCAAAGAATGCGAAGCAACCAGAGCGTGAAGAAAAGCGGGTTTTGGGTCTGGTG
TTGCTGCGTGGGGAGAACTTGGTATCCATGACTGTGGAGGGGCCACCCCCCAAAGATACTGGCATTGCTC
GGGTACCACTTGCTGGAGCTGCTGGAGGCCCTGGGGTTGGTAGGGCAGCTGGTAGAGGAGTACCAGCTGG
TGTGCCAATTCCCCAGGCCCCTGCTGGATTGGCAGGCCCTGTCCGAGGAGTTGGGGGACCATCCCAGCAG
GTAATGACTCCACAGGGAAGAGGCACTGTAGCAGCTGCTGCTGTTGCTGCGACTGCCAGTATTGCTGGAG
CCCCAACACAGTACCCACCAGGACGGGGCACTCCGCCCCCACCCGTCGGCAGAGCAACCCCACCTCCAGG
CATTATGGCTCCTCCACCTGGTATGAGACCACCCATGGGCCCACCAATTGGGCTTCCCCCTGCTCGAGGG
ACGCCAATAGGCATGCCGCCTCCGGGAATGAGACCCCCTCCACCAGGCATTAGAGGTCCACCTCCCCCAG
GAATGCGTCCACCAAGACCTTAG


>OriGene 5' read for NM_022808 unedited
GTATTTGTATACGACTCACTATAGGGCGGCCGCGCAATTCGCACGAGGGAGCCTTCTGTG
TGGTTTGCGGGGGCAAGGTCAGCTGCCCCCTGCCCTCTCTCTGGGGCTATTTGAGGAATG
CGGCCTTTTTGCATAAGAAAGGCTTTTCTCTACAGTAACTGTGGTCGCTGATCAATGACA
CCTTCCTGATGTAAGTGGGATCTGTGGATCTGAAAATTCACAGTGGCCAGCTCACCACCA
CCTGATGAAAGATACACCACAGGGTGAGAGCATCCTAACAGCAAACTGCAAATGAGATAC
TTTGACGAAGGTAATTGGGACTCCCATCAAGTCTCCACACAGCTAGCAGCCACGTGGGGC
ACTTCTCCAGCATATGTAAGTGGAACTCAGAAGGCAACATTCCCTGAACATACTCTTCCA
CCAGAATCTCCTCTACAGATTTTTGCTGCCCCTTTTACCAGTGGCTGAATCTACTTTCTC
TTATGGATCGCTTACACCTGAGACGAACTACAGAACAGCACGTACCAGAGGTGGAAGTCC
AAGTCAAACGCAGAAGGACTGCCTCACTGAGCAACCAAGAGTGTCAGTTGTACCCGAGGC
GTTCTCAGCAGCAGCAAGTACCTGTGGTGGATNNTCCAGCTGAACTGAGGCANGCATTTC
TAGCTGAGACACCAAGAAGTGGTTAAAGCCATATTGGAGTAGCGAGGAATCTGATTCCAA
GCAAAACCCAGCTCCATCTACTCTTTGAAGCTTCTGCCCAGCTTGCATTGTTTCTAAGAG
ACCTGCGGTATACCTTTATCTATAGCCTTCCCCTAGTTCTTCAGAGCATCAATTTTAACT
GTGGACATTGAATTTGTGGGACCGCAATCATGACTGTGGCCAAGATANCAGATGCTGCAG
CCATTGCTATAGAATGAATGATCCTGCAAGAGGCCGAATCCCATG
>OriGene 3' read for NM_022808 unedited
CGGCACGCAATCTAGTATCGAGTTTTTTTTTTTTTTTTTTAATTGCTCTATGCATTTATT
ATTAGCTATTATTAATGCAGAATGAGGGAACAAAAAGCTCACAAACACTCTACACAATTT
CACAAGACGCATTGCAGGGGAAAAAGTGACTGAGATGGATCAACAGTATGCTAAGGTCTT
GGTGGACGCATTCCTGGGGGAGGTGGACCTCTAATGCCTGGTGGAGGGGGTCTCATTCCC
GGAGGCGGCATGCCTATTGGCGTCCCTCGAGCAGGGGGAAGCCCAATTGGTGGGCCCATG
GGTGGTCTCATACCAGGTGGAGGAGCCATAATGCCTGGAGGTGGGGTTGCTCTGCCGACG
GGTGGGGGCGGAGTGCCCCGTCCTGGTGGGTACTGTGTTGGGGCTCCAGCAATACTGGCA
GTCGCAGCAACAGCAGCAGCTGCTACAGTGCCTCTTCCCTGTGGAGTCATTACCTGCTGG
GATGGTCCCCCAACTCCTCGGACAGGGCCTGCCAATCCAGCAGGGGCCTGGGGAATTGGC
ACACCAGCTGGTACTCCTCTACCAGCTGCCCTACCAACCCCAGGGCCTCCAGCAGCTCCA
GCAAGTGGTACCCGAGCAATGCCAGTATCTTTGGGGGGTGGCCCCTCCACAGTCATGGAT
ACCAAGTTCTCCCCACGCAGCATCACCAGACCCAAAACCCGCTTTTCTTCACGCTCTGGT
TGCTTCGCATTCTTTGGCTTGATCTTTCTGAACTCATCACAATCACAGAGGATCAAATTC
ATATGCTTGTCAAAGCNCTTAAAGTGCCAATGAAGATTCGGCCATCTTGCAGGATACATC
TCATTCTATAGNCAATGGGCTGCAGCATCTTGCTACTCTTGCCACAGTCATGGATTGCTG
TCCACCAATCCATGTCCACAGTAAACTTGAGCTTCTGAAACTAGGGAAGCTTANNATAAG
CTGACGCAGTTCTCTAT
Restriction Sites NotI-NotI     
ACCN NM_022808
Insert Size 1820 bp
OTI Disclaimer Our molecular clone sequence data has been matched to the reference identifier above as a point of reference. Note that the complete sequence of our molecular clones may differ from the sequence published for this corresponding reference, e.g., by representing an alternative RNA splicing form or single nucleotide polymorphism (SNP).
Product Components The ORF clone is ion-exchange column purified and shipped in a 2D barcoded Matrix tube containing 10ug of transfection-ready, dried plasmid DNA (reconstitute with 100 ul of water).
Reconstitution 1. Centrifuge at 5,000xg for 5min.
2. Carefully open the tube and add 100ul of sterile water to dissolve the DNA.
3. Close the tube and incubate for 10 minutes at room temperature.
4. Briefly vortex the tube and then do a quick spin (less than 5000xg) to concentrate the liquid at the bottom.
5. Store the suspended plasmid at -20°C. The DNA is stable for at least one year from date of shipping when stored at -20°C.
Reference Data
RefSeq NM_022808.2, NP_073719.1
RefSeq Size 1643 bp
RefSeq ORF 723 bp
Locus ID 6638
UniProt ID P63162
Domains Sm
Protein Families Stem cell - Pluripotency
Gene Summary This gene is located within the Prader-Willi Syndrome critical region on chromosome 15 and is imprinted and expressed from the paternal allele. It encodes a component of the small nuclear ribonucleoprotein complex, which functions in pre-mRNA processing and may contribute to tissue-specific alternative splicing. Alternative promoter use and alternative splicing result in a multitude of transcript variants encoding the same protein. Transcript variants that initiate at the CpG island-associated imprinting center may be bicistronic and also encode the SNRPN upstream reading frame protein (SNURF) from an upstream open reading frame. In addition, long spliced transcripts for small nucleolar RNA host gene 14 (SNHG14) may originate from the promoters at this locus and share exons with this gene. Alterations in this region are associated with parental imprint switch failure, which may cause Angelman syndrome or Prader-Willi syndrome. [provided by RefSeq, Mar 2017]
Transcript Variant: This variant (5) represents use of an alternate upstream promoter compared to variant 1. Sequence Note: This RefSeq record was created from transcript and genomic sequence data to make the sequence consistent with the reference genome assembly. The genomic coordinates used for the transcript record were based on transcript alignments.
*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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