NR2F2 (NM_021005) Human Untagged Clone

CAT#: SC108069

NR2F2 (untagged)-Human nuclear receptor subfamily 2, group F, member 2 (NR2F2), transcript variant 1

Specifications

Product Data

• Type: Human Untagged Clone
• Tag: Tag Free
• Symbol: NR2F2
• Synonyms: ARP-1; ARP1; CHTD4; COUPTF2; COUPTFB; COUPTFII; NF-E3; SVP40; TFCOUP2
• Vector: pCMV6-XL5
• E. coli Selection: Ampicillin (100 ug/mL)
• Mammalian Cell Selection: None
• Sequence Data:
  Fully Sequenced ORF

  >NCBI ORF sequence for NM_021005, the custom clone sequence may differ by one or more nucleotides
  
  
  ATGGCAATGGTAGTCAGCACGTGGCGCGACCCCCAGGACGAGGTGCCCGGCTCACAGGGCAGCCAGGCCT
  CGCAGGCGCCGCCCGTGCCCGGCCCGCCGCCCGGCGCCCCGCACACGCCACAGACGCCCGGCCAAGGGGG
  CCCAGCCAGCACGCCAGCCCAGACGGCGGCCGGTGGCCAGGGCGGCCCTGGCGGCCCGGGTAGCGACAAG
  CAGCAGCAGCAGCAACACATCGAGTGCGTGGTGTGCGGAGACAAGTCGAGCGGCAAGCACTACGGCCAGT
  TCACGTGCGAGGGCTGCAAGAGCTTCTTCAAGCGCAGCGTGCGGAGGAACCTGAGCTACACGTGCCGCGC
  CAACCGGAACTGTCCCATCGACCAGCACCATCGCAACCAGTGCCAGTACTGCCGCCTCAAAAAGTGCCTC
  AAAGTGGGCATGAGACGGGAAGCGGTGCAGAGGGGCAGGATGCCGCCGACCCAGCCGACCCACGGGCAGT
  TCGCGCTGACCAACGGGGATCCCCTCAACTGCCACTCGTACCTGTCCGGATATATTTCCCTGCTGTTGCG
  CGCGGAGCCCTATCCCACGTCGCGCTTCGGCAGCCAATGCATGCAGCCCAACAACATCATGGGTATCGAG
  AACATTTGCGAACTGGCCGCGAGGATGCTCTTCAGCGCCGTCGAGTGGGCCCGGAACATCCCCTTCTTCC
  CCGACCTGCAGATCACGGACCAGGTGGCCCTGCTTCGCCTCACCTGGAGCGAGCTGTTTGTGTTGAATGC
  GGCGCAGTGCTCCATGCCCCTCCACGTCGCCCCGCTCCTGGCCGCCGCCGGCCTGCATGCTTCGCCCATG
  TCCGCCGACCGGGTGGTCGCCTTTATGGACCACATACGGATCTTCCAAGAGCAAGTGGAGAAGCTCAAGG
  CGCTGCACGTTGACTCAGCCGAGTACAGCTGCCTCAAGGCCATAGTCCTGTTCACCTCAGATGCCTGTGG
  TCTCTCTGATGTAGCCCATGTGGAAAGCTTGCAGGAAAAGTCTCAGTGTGCTTTGGAAGAATACGTTAGG
  AGCCAGTACCCCAACCAGCCGACGAGATTCGGAAAGCTTTTGCTTCGCCTCCCTTCCCTCCGCACCGTCT
  CCTCCTCAGTCATAGAGCAATTGTTTTTCGTCCGTTTGGTAGGTAAAACCCCCATCGAAACCCTCATCCG
  GGATATGTTACTGTCCGGCAGCAGTTTTAACTGGCCGTATATGGCAATTCAATAA
  
  
  5' Read Nucleotide Sequence

  >OriGene 5' read for NM_021005 unedited
  TAAAATTTGTATACGACTCATATAGGCGGCCGCGACATTCGCACGAGGCTTCTGTCTTGA
  AGCCAGACAATCGACTTCAGCTCTCCCTCCCCTCCCTCTTTCTCCACGTTCTGCTCCCAC
  TCGCTCTCCTGTCCCCTTCCCCTCCCCTCCCGGCGGAAAGCCCCCCGAAACCAACAAAGC
  TGAGCCGAGAGAAACAAACAAAACAAACACACCGGGCCAGACAAGCCATCGACAAAACTT
  TGCAAAAGCAAAAACAAAAAAGGAAAAACTAACCAACCTCAACCAACCAGCCCCCGAGCC
  ACCCGGGGCGCCCTCCCGCGCCCTCTTGCACCCTCGCACACACAAAAGGCGGCGCGCCGG
  AGCCCGAGACCCGGGGAGCCGCCGCCGCCCCGCCGCCGCCCGCAGCCAGGGGAGCAGGAA
  GTCCGGACGCAGCCCCCATAGATATGGCAATGGTAGTCAGCACGTGGCGCGACCCCCAGG
  ACGAGGTGCCCGGCTCACAGGGCAGCCAGGCCTCGCAGGCGCCGCCCGTGCCCGGCCCGC
  CGCCCGGCGCCCCGCACACGCCACAGACGCCCGGCCAAGGGGGCCCAGCCAGCACGCCAG
  CCCAGACGGCGGCCGGTGGCCAGGGCGGCCCTGGCGGCCCGGGTAGCGACAAGCAGCAGC
  AGCAGCAACACATCGAGTGCGTGGTGTGCGGAGACAAGTCGAGCGGCAAGCACTACGGCC
  AGTTCACGTGCGAAGGCTGNCAGAGCTTCTTCAAGCGCAGCGTGCGGAGGAACCTGAGCT
  ACACGTGCCGCGCCAACCGGAACTGTCCCATCGACCAGCACCATCGCAACCAGTGCCAGT
  ACTGCCGCCTCANAAGTGCCTCAAAGTGGGCATGAAACGGGAAAGCGTGCANNAGGGCAG
  GATGCCGNCGACCCANCCGACCACGGGCAGTTNGCGCTGACAACGGGGATCCCTCACT
  
  3' Read Nucleotide Sequence

  >OriGene 3' read for NM_021005 unedited
  GGACGCGGCCGCAATCTANATCGAGTTTTTTTTTTTTTTTTTTGAAATTACAGTCCATTA
  AATTCTTCCCCTCTCTTCTTTTAGCAAACTTGTAACATCCTTTTATACCCTTTCTTAACA
  GAAGGAAATTAAGCAAACAAACCAGTCTTTTGCCTTTTCTTTCTCTGTTTCACTCCCCCT
  TCTTATTTTATTTATTTATTGAATTGCCATATACGGCCAGTTAAAACTGCTGCCGGACAG
  TAACATATCCCGGATGAGGGTTTCGATGGGGGTTTTACCTACCAAACGGACGAAAAACAA
  TTGCTCTATGACTGAGGAGGAGACGGTGCGGAGGGAAGGGAGGCGAATCAAAAGCTTTCC
  GAATCTCGCCGGCTGGTTGGGGTACTGGCTCCTAACGTATTCTTCCAAAGCACACTGAGA
  CTTNTCCTGCAAGCTTTCCACATGGGCTACATCAGAGAGACCACAGGCATCTGAGGTGAA
  CAGGACTATGGCCTTGAGGCAGCTGTACTCGGCTGAGCAACGTGCAGCGCCTTGAGCTTC
  TTCACTTGCTCTTGGAAGACCGTATGTGGTCCATAAAGGCGACCACCCGGCCGGCGGACA
  TGGGCGAAGCATGCAGGCCGGCGGCGGCCATAACCGGTGCGACTTGGAGGGGCATGGACC
  ACTGCGCCGAATTAACACAAACAGCTCGCTTCAGGTGAGGCGAAGCAGCGCACCTTGTCC
  CTGATCTGCAAGTCCGGGAAGAATGCGATGTCCCGGCCCCCTCGACAGCGCTGAAAGCTT
  CCTCCGGGCCAGTTCCAAATGTTCCGAACCCAAGATGTTGCCGCGCTGATGCCTTGCCTG
  CCCAACCGGACTGGGAAATGCCTCCGCCCCACAAGCCGGGAAATTATTCCGCACGTTCCC
  AGGGGAATCTGAGGGGATCCCCTTGGCACACCCAACTGCCCGGGTCCGTTGTGGCCGGGG
  AATCTCGACCTTTGGCCGCTTATCGTCTATGCACATCT
  
• Restriction Sites: NotI-NotI
• ACCN: NM_021005
• Insert Size: 2000 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 cDNA clone is shipped in a 2-D bar-coded Matrix tube as dried plasmid DNA. The package also includes 100 pmols of both the corresponding 5' and 3' vector primers in separate vials. Every lot of primer is tested to provide clean sequencing of OriGene TrueClones.
• 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_021005.2, NP_066285.1
• RefSeq Size: 3049 bp
• RefSeq ORF: 1245 bp
• Locus ID: 7026
• Cytogenetics: 15q26.2
• Domains: HOLI, zf-C4
• Protein Families: Druggable Genome, Nuclear Hormone Receptor, Transcription Factors
• Gene Summary: 'This gene encodes a member of the steroid thyroid hormone superfamily of nuclear receptors. The encoded protein is a ligand inducible transcription factor that is involved in the regulation of many different genes. Alternate splicing results in multiple transcript variants. [provided by RefSeq, Mar 2010]'
  Transcript Variant: This variant (1) represents the longest transcript and encodes the longest 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.