PRMT7 (NM_019023) Human Untagged Clone

CAT#: SC125318

PRMT7 (untagged)-Human protein arginine methyltransferase 7 (PRMT7), transcript variant 1


  "NM_019023" in other vectors (7)

Reconstitution Protocol

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Size
    • 10 ug

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Specifications

Product Data
Type Human Untagged Clone
Tag Tag Free
Symbol PRMT7
Synonyms SBIDDS
Vector pCMV6-XL4
E. coli Selection Ampicillin (100 ug/mL)
Mammalian Cell Selection None
Sequence Data
>OriGene ORF within SC125318 sequence for NM_019023 edited (data generated by NextGen Sequencing)
ATGAAGATCTTCTGCAGTCGGGCCAATCCGACCACGGGGTCTGTGGAGTGGCTGGRGGAG
GATGAACACTATGATTACCACCAGGAGATTGCAAGGTCATCTTATGCAGATATGCTACAT
GACAAAGACAGAAATGTAAAATACTACCAAGGTATCCGGGCTGCCGTGAGCAGGGTGAAG
GACAGAGGACAGAAGGCCTTGGTTCTCGACATTGGCACTGGCACGGGACTCTTGTCAATG
ATGGCGGTCACAGCAGGTGCCGACTTCTGCTATGCCATCGAGGTTTTCAAGCCTATGGCT
GATGCTGCTGTGAAGATTGTGGAGAAAAATGGCTTTAGTGATAAGATTAAGGTTATCAAC
AAGCATTCCACCGAGGTGACTGTAGGTCCAGAGGGTGACATGCCATGCCGTGCCAACATC
CTGGTCACAGAGTTGTTTGACACAGAGCTGATCGGGGAGGGGGCGCTGCCCTCCTATGAG
CACGCACACAGGCATCTCGTGGAGGAAAATTGTGAGGCCGTGCCCCACAGAGCCACCGTC
TATGCACAGCTGGTGGAGTCCGGGAGGATGTGGTCGTGGAACAAGCTATTTCCCATCCAC
GTGCAGACCAGCCTCGGAGAGCAGGTCATCGTCCCTCCCGTTGACGTGGAGAGCTGCCCT
GGCGCACCCTCTGTCTGTGACATTCAGCTGAACCAGGTGTCACCAGCCGACTTTACAGTC
CTCAGCGATGTGCTGCCCATGTTCAGCATAGACTTCAGCAAGCAAGTCAGTAGCTCAGCA
GCCTGCCATAGCAGGCGGTTTGAACCTCTGACATCTGGCCGAGCTCAGGTGGTTCTCTCG
TGGTGGGACATTGAAATGGACCCTGAGGGGAAGATCAAGTGCACCATGGCCCCCTTCTGG
GCACACTCAGACCCAGAGGAGATGCAGTGGCGGGACCACTGGATGCAGTGTGTGTACTTC
CTGCCACAAGAGGAGCCTGTGGTGCAGGGCTCAGCGCTCTATCTGGTAGCCCACCACGAT
GACTACTGCGTATGGTACAGCCTGCAGAGGACCAGCCCTGAAAAGAATGAGAGAGTCCGC
CAGATGCGCCCCGTGTGTGACTGCCAGGCTCACCTGCTCTGGAACCGGCCTCGGTTTGGA
GAGATCAATGACCAGGACAGAACTGATCGATACGTCCAGGCTCTGAGGACCGTGCTGAAG
CCAGACAGCGTGTGCCTGTGTGTCAGCGATGGCAGCCTGCTCTCCGTGCTGGCCCATCAC
CTGGGGGTGGAGCAGGTGTTTACAGTCGAGAGTTCAGCAGCTTCTCACAAACTGTTGAGA
AAAATCTTCAAGGCTAACCACTTGGAAGATAAAATTAACATCATAGAGAAACGGCCGGAA
TTATTAACAAATGAGGACCTACAGGGCAGAAAGGTCTCTCTCCTCCTGGGCGAGCCGTTC
TTCACTACCAGCCTGCTGCCGTGGCACAACCTCTACTTCTGGTACGTGCGGACCGCTGTG
GACCAGCACCTGGGGCCAGGTGCCATGGTGATGCCCCAGGCAGCCTCGCTGCACGCTGTG
GTTGTGGAGTTCAGGGACCTGTGGCGGATCCGGAGCCCCTGTGGTGACTGCGAAGGCTTC
GACGTGCACATCATGGACGACATGATTAAGCGTGCCCTGGACTTCAGGGAGAGCAGGGAA
GCTGAGCCCCACCCGCTGTGGGAGTACCCATGCCGCAGCCTCTCCGAGCCCTGGCAGATC
CTGACCTTTGACTTCCAGCAGCCGGTGCCCCTGCAGCCCCTGTGTGCCGAGGGCACTGTG
GAGCTCAGAAGGCCCGGGCAGAGCCACGCAGCGGTGCTATGGATGGAGTACCACCTGACC
CCGGAGTGCACGCTCAGCACTGGCCTCCTGGAGCCTGCAGACCCCGAGGGGGGCTGCTGC
TGGAACCCCCACTGCAAGCAGGCCGTCTACTTCTTCAGCCCTGCCCCAGATCCCAGAGCA
CTGCTGGGTGGCCCACGGACTGTCAGCTATGCAGTGGAGTTTCACCCCGACACAGGCGAC
ATCATCATGGAGTTCAGGCATGCAGATACCCCAGACTGA

Clone variation with respect to NM_019023.2
56 a=>r;1797 c=>t
>OriGene 5' read for NM_019023 unedited
GGGCGGTCAGGAATTGTATACGACTCACTATAGGCGGCCGCGAATTCGCACGAGCCCGCC
TGCTGGCCGCGGTAAAATGGTAGCAGCGGAGGCGAGCGGAGGGTTTCCCGCGGCGGGTGA
GGCGCTGGATTTCTGACAGTCAGACTTGTCCACAAGAACTCAACTGGCAAGGCTGCTTTT
CTGTGCTAAAACTGGGGAGCTAGTGGGCACCATGAAGATCTTCTGCAGTCGGGCCAATCC
GACCACGGGGTCTGTGGAGTGGCTGGAGGAGGATGAACACTATGATTACCACCAGGAGAT
TGCAAGGTCATCTTATGCAGATATGCTACATGACAAAGACAGAAATGTAAAATACTACCA
AGGTATCCGGGCTGCCGTGAGCAGGGTGAAGGACAGAGGACAGAAGGCCTTGGTTCTCGA
CATTGGCACTGGCACGGGACTCTTGTCAATGATGGCGGTCACAGCAGGTGCCGACTTCTG
CTATGCCATCGAGGTTTTCAAGCCTATGGCTGATGCTGCTGTGAAGATTGTGGAGAAAAA
TGGCTTTAGTGATAAGATTAAGGTTATCAACAAGCATTCCACCGAGGTGACTGTAGGTCC
AGAGGGTGACATGCCATGCCGTGCCAACATCCTGGTCACAGAGTTGTTTGACACAACTGG
ATCGGGGAGGGGGCGCTGCCCTCCTATGAGCACGCACACAGGCATCTCGTGGAGGAAAAT
TGTGAGGCCGTGCCCCACAGAGCCACCGTCTATGCACAGCTGGNTGGAGTCCGGNAAGAT
GTNGTTCGTGGAACAAGCTATTTCCATNCACGTGCAGACCAGCCTCGNAGAAGCAGTCAT
CGTCCCTCCCGTTGACGTGNAGAGCTGCCCTGGCGCACCCTCTGTCTGTGACATTCAGCT
GAACCCAGTGTCACCAN
>OriGene 3' read for NM_019023 unedited
TTCCTCAGGCCACTTTATGCTCAGNATGGTCAGTCTGGGGTATCTGCATGCCTGAACTCC
ATGATGATGTCGCCTGTGTCGGGGTGAAACTCCACTGCATAGCTGACAGTCCGTGGGCCA
CCCAGCAGTGCTCTGGGATCTGGGGCAGGGCTGAAGAAGTAGACGGCCTGCTTGCAGTGG
GGGTTCCAGCAGCAGCCCCCCTCGGGGTCTGCAGGCTCCAGGAGGCCAGTGCTGAGCGTG
CACTCCGGGGTCAGGTGGTACTCCATCCATAGCACCGCTGCGTGGCTCTGCCCGGGCCTT
CTGAGCTCCACAGTGCCCTCGGCACACAGGGGCTGCAGGGGCACCGGCTGCTGGAAGTCA
AAGGTCAGGATCTGCCAGGGCTCGGAGAGGCTGCGGCATGGGTACTCCCACAGCGGGTGG
GGCTCAGCTTCCCTGCTCTCCCTGAAGTCCAGGGCACGCTTAATCATGTCGTCCATGATG
TGCACGTCGAAGCCTTCGCAGTCACCACAGGGGCTCCGGATCCGCCACAGGTCCCTGAAC
TCCACAACCACAGCGTGCAGCGAGGCTGCCTGGGGCATCACCATGGCACCTGGCCNCAGG
TGCTGGTCCACAGCGGTCCGCACGTACCAGAAGTAGAGGTTGTGCCACGGCAGCAGGCTG
GTAGTGAAGAACGGCTCGCCCAGNANGAGAGAGACCCTTCTGCCCTGTANGTCCTCATTT
GTTAATAATTCCCGCCGTTTCTCTATGATGGTAATTTNTATCTCCAAGTGGTTAGCCTTG
AAAGATTTTCTCACAGTTTGTGAGGAGCTGCTGAACTCTCGACTGTAAACACCCTGCTCA
CCCCCAGGTGATGGCCAGCACCGAGAGCAGGCTGCATCGCTGACCCCAAGCCCACGCTGG
CTGGGTTCAGAACGGTCTCAGACCTGGACTTTCGATCAGTTCTGTCTGTCAA
Restriction Sites ECoRI-NOT     
ACCN NM_019023
ORF Size 2079 bp
Insert Size 2500
OTI Disclaimer Due to the inherent nature of this plasmid, standard methods to replicate additional amounts of DNA in E. coli are highly likely to result in mutations and/or rearrangements. Therefore, OriGene does not guarantee the capability to replicate this plasmid DNA. Additional amounts of DNA can be purchased from OriGene with batch-specific, full-sequence verification at a reduced cost. Please contact our customer care team at custsupport@origene.com or by calling 301.340.3188 option 3 for pricing and delivery.

The molecular sequence of this clone aligns with the gene accession number as a point of reference only. However, individual transcript sequences of the same gene can differ through naturally occurring variations (e.g. polymorphisms), each with its own valid existence. This clone is substantially in agreement with the reference, but a complete review of all prevailing variants is recommended prior to use. More info
Reference Data
RefSeq NM_019023.1, NP_061896.1
RefSeq Size 2390
RefSeq ORF 2079
Locus ID 54496
Protein Families Druggable Genome
Gene Summary This gene encodes a member of the protein arginine N-methyltransferase family of proteins. The encoded enzyme transfers single methyl groups to arginine residues to generate monomethylarginines on histone proteins as well as other protein substrates. This enzyme plays a role in a wide range of biological processes, including neuronal differentiation, male germ line imprinting, small nuclear ribonucleoprotein biogenesis, and regulation of the Wnt signaling pathway. Mutations in this gene underlie multiple related syndromes in human patients characterized by intellectual disability, short stature and other features. The encoded protein may promote breast cancer cell invasion and metastasis in human patients. [provided by RefSeq, May 2017]
Transcript Variant: This variant (1) includes a 3' terminal exon that extends past a splice site that is used in variant 4, which results in a novel 3' coding region and 3' UTR compared to variant 4. The encoded isoform (1) is shorter and has a distinct C-terminus compared to isoform 4. Both variants 1 and 3 encode the same isoform (1).

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