Zinc finger protein 287 (ZNF287) (NM_020653) Human Untagged Clone

CAT#: SC113072

ZNF287 (untagged)-Human zinc finger protein 287 (ZNF287)

Specifications

Product Data

• Type: Human Untagged Clone
• Tag: Tag Free
• Symbol: ZNF287
• Synonyms: ZKSCAN13; ZSCAN45
• Vector: pCMV6-XL4
• E. coli Selection: Ampicillin (100 ug/mL)
• Mammalian Cell Selection: None
• Sequence Data:
  Fully Sequenced ORF

  >OriGene ORF within SC113072 sequence for NM_020653 edited (data generated by NextGen Sequencing)
  ATGTTAGCCTCAAGCAAGAGGATGAACAGTTCTTCACGTTCTCAAATCCTTCTAAGGTGG
  AAGTCAGACAAGGCTCAGAGTGGACCCTACAATGTTGAGAAGGAAATCCTTACTTCAAGA
  TTCTTGCGTGACACTGAGACCTGTCGACAGAATTTTAGGAATTTTCCATACCCAGACCTG
  GCTGGTCCTCGAAAGGCATTGAGTCAACTCCGAGAGCTCTGCCTTAAGTGGCTGAGACCT
  GAGATTCACTCAAAGGAACAAATTTTGGAGCTGCTGGTGCTGGAGCAATTCCTGACCATC
  CTGCCTGGTGAGGTTAGGACTTGGGTAAAGTCCCAGTATCCAGAGAGCAGCGAGGAAGCA
  GTGACTCTGGTGGAGGATTTGACTCAGATTCTAGAAGAGGAAGCTCCTCAAAACTCTACC
  CTTTCCCAAGATACCCCAGAGGAAGACCCCAGAGGAAAACATGCTTTCCAGACAGGATGG
  CTAAATGACTTGGTGACCAAAGAATCGATGACATTCAAAGATGTGGCTGTAGACATCACC
  CAGGAGGACTGGGAGTTAATGCGTCCTGTGCAGAAGGAATTATACAAGACTGTGACGTTA
  CAGAACTATTGGAACATGGTTTCTCTGGGACTTACAGTGTACAGACCAACTGTGATTCCC
  ATATTGGAAGAACCATGGATGGTGATAAAAGAAATTTTAGAAGGCCCTAGTCCAGAATGG
  GAAACTAAAGCCCAAGCATGTACTCCAGTGGAGGATATGTCTAAACTCACAAAGGAAGAA
  ACCCATACCATCAAATTAGAAGACTCATATGACTACGATGATAGACTAGAGAGGCGAGGA
  AAAGGTGGCTTCTGGAAAATTCACACTGATGAAAGAGGTTTCAGTTTGAAGTCAGTCCTT
  TCACAAGAATATGATCCTACAGAAGAATGTCTTAGTAAATATGATATATATAGAAATAAT
  TTTGAAAAGCATTCAAACCTAATTGTACAGTTTGATACCCAATTAGATAATAAAACTTCT
  GTGTATAATGAAGGCAGGGCAACCTTCAATCATGTCTCATATGGTATTGTACATAGGAAA
  ATACTTCCTGGAGAGAAGCCTTACAAGTGTAATGTGTGTGGGAAAAAATTTAGGAAATAC
  CCATCCCTCCTGAAACACCAAAGTACCCATGCCAAAGAGAAATCGTATGAATGTGAAGAA
  TGTGGGAAAGAGTTTAGGCATATCTCATCCCTTATTGCACATCAGAGAATGCACACTGGA
  GAAAAACCATATGAATGCCACCAGTGTGGTAAAGCCTTCAGCCAGCGTGCACACCTTACT
  ATACATCAGAGAATTCATACTGGAGAGAAACCCTATAAGTGTGATGACTGTGGGAAAGAC
  TTCAGTCAGCGTGCACACCTTACCATCCATCAAAGGACACATACTGGAGAGAAACCATAT
  AAATGCTTGGAATGTGGTAAAACCTTCAGTCATAGTTCATCACTGATTAATCATCAGAGA
  GTTCATACTGGAGAAAAACCTTATATATGCAATGAATGTGGGAAGACTTTCAGTCAGAGT
  ACACACCTTCTTCAGCATCAAAAAATACATACTGGGAAGAAACCATATAAATGCAATGAA
  TGTTGGAAAGTGTTTAGTCAGAGTACTTACCTTATTCGACATCAGAGAATTCATTCTGGA
  GAGAAGTGTTATAAATGTAATGAATGTGGAAAAGCCTTTGCTCATTCCTCAACCCTTATT
  CAACATCAAACCACTCACACTGGAGAGAAATCCTATATATGTAATATATGTGGGAAAGCC
  TTCAGCCAGAGTGCAAATCTTACTCAACATCATAGAACACATACTGGAGAGAAACCATAT
  AAATGCAGTGTGTGTGGGAAAGCATTCAGCCAGAGTGTGCACCTTACTCAACATCAGAGG
  ATTCATAATGGAGAAAAACCCTTTAAATGCAATATATGTGGGAAAGCATATAGACAAGGC
  GCAAATCTTACTCAGCATCAAAGGATTCATACTGGAGAAAAACCCTATAAATGTAATGAA
  TGTGGGAAAGCTTTCATTTATTCCTCATCACTTAATCAACATCAGAGAACTCATACTGGA
  GAGAGACCCTATAAATGTAATGAATGTGATAAGGATTTTAGCCAGAGAACATGCCTTATT
  CAACACCAGAGAATTCACACAGGAGAGAAACCCTATGCATGTCGTATATGTGGTAAAACC
  TTCACCCAGAGTACAAACCTTATTCAGCATCAACGTGTTCATACAGGTGCCAAACATCGT
  AATTAA
  
  Clone variation with respect to NM_020653.2
  
  5' Read Nucleotide Sequence

  >OriGene 5' read for NM_020653 unedited
  TATTTTGTAATACGACTCACTATAGGGCGGCCGCGAATTCGGCACCAGCCGAGGCGAGGT
  CGCGGCTAAGCAGAGGCGCCGGGGTTTCTGGGCCGGGCTTCTCAGGACCGGGCTGGAACG
  TGCAGCTCCTGGCCGGGACACTCTGTGCTTTGCGGGGAAGGGAAGTGGCGGAGCCCGAGG
  ATCCGCTGCCGCTCGGGACTGAGCCCGCCACGCAGGCGCCTGTGCCAGCGTCGCCATTGT
  TGCCTGTGGCCTTAGGGCCGCTCCGGCTGCCCGTCGGCCGGGTCCCAGCGACAGCTCCAT
  CCCCCACCAACCCCAAGCAGATGGCAGTTCCCTTACAAGTCTAAGGATATAGGGGAGGAA
  GACAAGGGTCTCTTATCCATCCCTGCAAGTTCTGGGCTCAGAATTTGTCACTAAGGCTGC
  TAACTCTACCTTGATTCTGTTCTGCCCTCGGCTGCAGCAGCCTTTGATATAGTGTCCTTG
  TGACTCTAGCATGAGACTTCAAGCAGTTGGCTCACTACTGGAGAAATAAAGGATATTGCC
  AGATTGACTCTCCTGTCTGTAGCAATGTTAGCCTCAAGCAAGAGGATGAACAGTTCTTCA
  CGTTCTCAAATCCTTCTAAGGTGGAAGTCAGACAAGGCTCAGAGTGGACCCTACAATGTT
  GAGAAGGAAATCCTTACTTCAAGATTCTTGCGTGACACTGAGACCTGTCGACAGAANTTT
  ANGAATTTTCCATACCCAGACCTGGCTGGTCCTCGAAAGGCATTGAGTCAACTCCGAGAG
  CTCTGCCTTAAGTGGCTGAGACCTGAGATTCACTCANAGGACAANATTTGGAGCTGCTGG
  TGCTGGNAGCATTCCTGACCTCCCTGCTGGTGAGGNTAGACTGGNGTAAGTCCCAGATCC
  ANAGAGCNCGAGAACCATGACTCTGTGGGAGATTGACTCAGATCTAGAGAGGAGCTCTCA
  AACCTACCTT
  
  3' Read Nucleotide Sequence

  >OriGene 3' read for NM_020653 unedited
  CTCTGTCCACGCGGCACGCAATCTAGAGATCGAGTTTTTTTTTTTTTTTTTTTTTTTTTT
  TTTTTTGAACTGGACAAATCCATTTATACTGGGAATTTTTTTTCCTCAACTGAACAGAAG
  TTTGAAAGCACATTATTCAGGGATGGGAAACCTGCATAAATGTAGGGCCTTTTCATATAC
  ACAGGTTCCACCAGGCTGACCGGGCAACTTGAGTATGGGTAGATTTTCGTATACATGGGG
  GGGCCTGGAACCAATCCCCCGAGTATACCAAAGGATAAGGGGACTTGAAATAAAAAGTTG
  ATGAGTTATGTTTTTGAATACCCTTCACAGGGTTTCTTTCTGGAATGAATTAAAATCATA
  TCAAATTAAGGGTAAAAAGCCAAGTTCCCTTCTTAAATTTCACATTAAATCTAAATAGGG
  TATATCCATACCACTACTTCTGATACTTCTGCTGAGTATCTAACATATTGCACTTCTTCA
  AACTTCTTCTGAATGTTCTGACCCATAGAATGCACAAAACAAAATTGAAACAAAGTTGTA
  AAACCGAATTGAAGTTTCCCTTATCCATTAATTACGATGTTTGGCACCTGTATGAACACG
  TTGATGCTGAATAAGGGTTGTACTCTGGGGGAAGGTTTTACCACATATACCACATGCATA
  GGGTTTCTCTCCTGAGAGAATTCTCTGGCGTTGAATAAAGCATGTTCCCTGGCTAAAATC
  CTTATCACATTCATTACATTTATAGGGGTCTCCTCTCCAGCATGGAGTCCTCTCGAGGTC
  GATTAAGCGGATGAAGGAATAAATGAAAGCCTCTCCCACATCTCATTACACTTTTATAGG
  TTTTCTCTTCCAGTATAGATACCTCTGGATGCTGGAAAAAATTAGCGCCCTTGTCTATTG
  GCTCTCCCACATATATTGGCATTTAAGAGGTTCTTTCCCCTTTAGAATCCCCTGAGGCTG
  AACAGAGCGCCCACCTCTGGCTGAATGCCTTCCCCC
  
• Restriction Sites: NotI-NotI
• ACCN: NM_020653
• ORF Size: 2265 bp
• Insert Size: 2940
• 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_020653.1, NP_065704.1
• RefSeq Size: 4278
• RefSeq ORF: 2265
• Locus ID: 57336
• Domains: KRAB, LER, zf-C2H2
• Protein Families: Transcription Factors
• Gene Summary: This gene encodes a member of the krueppel family of zinc finger proteins, suggesting a role as a transcription factor. Its specific function has not been determined. This gene is located near the Smith-Magenis syndrome region on chromosome 17. [provided by RefSeq, Jul 2008]
  Transcript Variant: This variant (2) differs in the 5' UTR compared to variant 1. Variants 1-4 all 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.