Matrin 3 (MATR3) (NM_018834) Human Untagged Clone

CAT#: SC113375

MATR3 (untagged)-Human matrin 3 (MATR3), transcript variant 2


  "NM_018834" in other vectors (4)

Reconstitution Protocol

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Size
    • 10 ug

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Specifications

Product Data
Type Human Untagged Clone
Tag Tag Free
Symbol MATR3
Synonyms ALS21; MPD2; VCPDM
Vector pCMV6-XL5
E. coli Selection Ampicillin (100 ug/mL)
Mammalian Cell Selection None
Sequence Data
>OriGene ORF within SC113375 sequence for NM_018834 edited (data generated by NextGen Sequencing)
ATGTCCAAGTCATTCCAGCAGTCATCTCTCAGTAGGGACTCACAGGGTCATGGGCGTGAC
CTGTCTGCGGCAGGAATAGGCCTTCTTGCTGCTGCTACCCAGTCTTTAAGTATGCCAGCA
TCTCTTGGAAGGATGAACCAGGGTACTGCACGCCTTGCTAGTTTAATGAATCTTGGAATG
AGTTCTTCATTGAATCAACAAGGAGCTCATAGTGCACTGTCTTCTGCTAGTACTTCTTCC
CATAATTTGCAGTCTATATTTAACATTGGAAGTAGAGGTCCACTCCCTTTATCTTCTCAA
CACCGTGGAGATGCAGACCAGGCCAGTAACATTTTGGCCAGCTTTGGTCTGTCTGCTAGA
GACTTAGATGAACTGAGTCGTTATCCAGAGGACAAGATTACTCCTGAGAATTTGCCCCAA
ATCCTTCTACAGCTTAAAAGGAGGAGAACTGAAGAAGGCCCTACCTTGAGTTATGGTAGA
GATGGCAGATCTGCTACACGGGAGCCACCATACAGAGTACCTAGGGATGATTGGGAAGAA
AAAAGGCACTTTAGAAGAGATAGTTTTGATGATCGTGGTCCTAGTCTCAACCCAGTGCTT
GATTATGACCATGGAAGTCGTTCTCAAGAATCTGGTTATTATGACAGAATGGATTATGAA
GATGACAGATTAAGAGATGGAGAAAGGTGTAGGGATGATTCTTTTTTTGGTGAGACCTCG
CATAACTATCATAAATTTGACAGTGAGTATGAGAGAATGGGACGTGGTCCTGGCCCCTTA
CAAGAGAGATCTCTCTTTGAGAAAAAGAGAGGCGCTCCTCCAAGTAGCAATATTGAAGAC
TTCCATGGACTCTTACCGAAGGGTTATCCCCATCTGTGCTCTATATGTGATTTGCCAGTT
CATTCTAATAAGGAGTGGAGTCAACATATCAATGGAGCAAGTCACAGTCGTCGATGCCAG
CTTCTTCTTGAAATCTACCCAGAATGGAATCCTGACAATGATACAGGACACACAATGGGT
GATCCATTCATGTTGCAGCAGTCTACAAATCCAGCACCAGGAATTCTGGGACCTCCACCT
CCCTCATTTCATCTTGGGGGACCAGCAGTTGGACCAAGAGGAAATCTGGGTGCTGGAAAT
GGAAACCTGCAAGGACCTAGACACATGCAGAAAGGCAGAGTGGAAACTAGCAGAGTTGTT
CACATCATGGATTTTCAACGAGGGAAAAACTTGAGATACCAGCTATTACAGCTGGTAGAA
CCATTTGGAGTCATTTCAAATCATCTGATTCTAAATAAAATTAATGAGGCATTTATTGAA
ATGGCAACCACAGAGGATGCTCAGGCCGCAGTGGATTATTACACAACCACACCAGCGTTA
GTATTTGGCAAGCCAGTGAGAGTTCATTTATCCCAGAAGTATAAAAGAATAAAGAAACCT
GAAGGAAAGCCAGATCAGAAGTTTGATCAAAAGCAAGAGCTTGGACGTGTGATACATCTC
AGCAATTTGCCGCATTCTGGCTATTCTGATAGTGCTGTTCTCAAGCTTGCTGAGCCTTAT
GGGAAAATAAAGAATTACATATTGATGAGGATGAAAAGTCAGGCTTTTATTGAGATGGAG
ACAAGAGAAGATGCAATGGCAATGGTTGACCATTGTTTGAAAAAAGCCCTTTGGTTTCAG
GGGAGATGTGTGAAGGTTGACCTGTCTGAGAAATATAAAAAACTGGTTCTGAGGATTCCA
AACAGAGGCATTGATTTACTGAAAAAAGATAAATCCCGAAAAAGATCTTACTCTCCAGAT
GGCAAAGAATCTCCAAGTGATAAGAAATCCAAAACTGATGGTTCCCAGAAGACTGAGAGT
TCAACCGAAGGTAAAGAACAAGAAGAGAAGTCCGGTGAAGATGGTGAGAAAGACACAAAG
GATGACCAGACAGAGCAGGAACCTAATATGCTTCTTGAATCTGAAGATGAGCTACTTGTA
GATGAAGAAGAAGCAGCAGCACTGCTAGAAAGTGGCAGTTCAGTGGGAGACGAGACCGAT
CTTGCTAATTTAGGTGATGTGGCTTCTGATGGGAAAAAGGAACCATCAGATAAAGCTGTG
AAAAAAGATGGAAGTGCTTCAGCAGCAGCAAAGAAAAAGCTTAAAAAGGTGGACAAGATC
GAGGAACTTGATCAAGAAAACGAAGCAGCGTTGGAAAATGGAATTAAAAATGAGGAAAAC
ACAGAACCAGGTGCTGAATCTTCTGAGAACGCTGATGATCCCAACAAAGATACAAGTGAA
AACGCAGATGGTCAAAGTGATGAGAACAAGGACGACTATACAATCCCAGATGAGTATAGA
ATTGGACCATATCAGCCCAATGTTCCTGTTGGTATAGACTATGTGATACCTAAAACAGGG
TTTTACTGTAAGCTGTGTTCACTCTTTTATACAAATGAAGAAGTTGCAAAGAATACTCAT
TGCAGCAGCCTTCCTCATTATCAGAAATTAAAGAAATTTCTGAATAAATTGGCAGAAGAA
CGCAGACAGAAGAAGGAAACTTAA

Clone variation with respect to NM_018834.5
>OriGene 5' read for NM_018834 unedited
TTGTAATACGACTCACTTATAGGGCGGCCGCGAATTCGCACGAGGTGGGAGTCTCCGCGT
CCCGCTCGCTGGGAGAGAGGTACCTCTCCTTTTCCCTCTCCCTTTCCCTAAGAGTTGTCT
GCTGGTTCTCAGCTTGAAGAAGATTCTGCAGTCCTTATTGATCCTTTTTCTTGGCGTTAC
CATTTTTGAAGCAAAGTTAACCTAGCTTTCTAGTTTGAGCTTTCTTTTTGGCCGTCTTTA
AAAAAATTTTTTTTTTTTAATCTATAAAATAGACAAGAGCTAGTTCTACAATGTCCAAGT
CATTCCAGCAGTCATCTCTCAGTAGGGACTCACAGGGTCATGGGCGTGACCTGTCTGCGG
CAGGAATAGGCCTTCTTGCTGCTGCTACCCAGTCTTTAAGTATGCCAGCATCTCTTGGAA
GGATGAACCAGGGTACTGCACGCCTTGCTAGTTTAATGAATCTTGGAATGAGTTCTTCAT
TGAATCAACAAGGAGCTCATAGTGCACTGTCTTCTGCTAGTACTTCTTCCCATAATTTGC
AGTCTATATTTAACATTGGAAGTAGAGGTCCACTCCCTTTATCTTCTCAACACCGTGGAG
ATGCAGACCAGGCCAGTAACATTTTGGCCAGCTTTGGTCTGTCTGCTAGAGACTTAGATG
AACTGAGTCGTTATCCAGAGGACAAGATTACTCCTGAGAATTTGCCCCANATCCTTCTAC
AGCTTAAAGGAGGAGAACTGAAGAAGGCCCTACCTTGAGTTATGGTAGAGATGGCAGATC
TGCTACCGGGAGCCACCTACAGAGTACCTAGGATGATTGGGAAGAAAAAGGCCTTTAAAG
AGATAGNNTTGATGATCGGGGNCCTAGTCTCAACCAGTGCTTGATATACCCTGGNAAGTC
GTCTCAGAATCTGGGTATATGACGAN
>OriGene 3' read for NM_018834 unedited
AACCCCTTGTCTNTGNNACCGCGGCCGCTTTTTNANGATCGNGTTTTTTTTTTTTTTTTT
TGGTTTTGTTCTTTATTGGAAGGAATAAAAGTTGACATTTCTTTGAAACTTGGAACTACT
AAATTTCATTTTTCCAAATGGTTCTACATTTTTTTCTTAGTGGTGCAAGTTGTCTTAAGT
AGCTTAGGAAGTCAATCTCTACAAAGTACTTCTGTCTGTTGCCATTCTGATAAAACAAAA
ACTATTCATTAACTTAACCATATGTGTATTTTTTTTGCTATAACACTTAACACATGAACA
GACATCTATTATTTCTCCACTAAAACAAAAGAGTACAATAGTTTTCTTCTAACTATCAGT
ATTGTATTTAAAAAAGGTTAACATTAAAAACAAAGAACCATTATTTTCTTTGAAATCATT
AAATCTCCTTGCACATCTTAAGTTTCCTTCTTCTGTCTGCGTTCTTCTGCCAATTTATTC
AGAAATTTCTTTAATTTCTGATAATGAGGAAGGCTGCTGCAATGAGTATTCTTTGCAACT
TCTTCATTTGTATAAAAGAGTGAACACAGCTTACAGTAAAACCCTGTTTTAGGTATCACA
TAGTCTATACCAACAGGAACATTGGGCTGATATGGTCCAATTCTATACTCATCTGGGATT
GTATAGTCGTCCTTGTTCTCATCACTTTGACCATCTGCGTTTTCACTTGTATCTTTGNTG
GGATCATCAGCGTTCTCAGAAGATTCACACCTGGCTCTGGGGTTTCCTCATTTTTAATTC
CATTTTCAACGCTGCTTTCGTTTCTTGATCAAGTTCCTCGAATCTGTCACCTTTTTAAGC
TTTTTTTTTGCTGCTGCTGAAACACTTCCATCTTTTTTCACAGNTTTACCTGAAGGG
Restriction Sites NotI-NotI     
ACCN NM_018834
ORF Size 2544 bp
Insert Size 1360
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).
Reference Data
RefSeq NM_018834.4, NP_061322.2
RefSeq Size 3921
RefSeq ORF 2544
Locus ID 9782
Domains RRM, ZnF_U1
Gene Summary This gene encodes a nuclear matrix protein, which is proposed to stabilize certain messenger RNA species. Mutations of this gene are associated with distal myopathy 2, which often includes vocal cord and pharyngeal weakness. Alternatively spliced transcript variants, including read-through transcripts composed of the upstream small nucleolar RNA host gene 4 (non-protein coding) and matrin 3 gene sequence, have been identified. Pseudogenes of this gene are located on chromosomes 1 and X. [provided by RefSeq, Aug 2013]
Transcript Variant: This variant (2) differs in the 5' UTR, compared to variant 1. Variants 1-4 encode the same isoform (a). 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.

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