REEP1 (NM_022912) Human Untagged Clone

CAT#: SC112404

REEP1 (untagged)-Human receptor accessory protein 1 (REEP1), nuclear gene encoding mitochondrial protein, transcript variant 2

Specifications

Product Data

• Type: Human Untagged Clone
• Tag: Tag Free
• Symbol: REEP1
• Synonyms: C2orf23; HMN5B; SPG31; Yip2a
• Vector: pCMV6-XL5
• E. coli Selection: Ampicillin (100 ug/mL)
• Mammalian Cell Selection: None
• Sequence Data:
  Fully Sequenced ORF

  >OriGene ORF within SC112404 sequence for NM_022912 edited (data generated by NextGen Sequencing)
  ATGGTGTCATGGATCATCTCCAGGCTGGTGGTGCTTATATTTGGCACCCTTTACCCTGCG
  TATTATTCCTACAAGGCTGTGAAATCAAAGGACATTAAGGAATATGTCAAATGGATGATG
  TACTGGATTATATTTGCACTTTTCACCACAGCAGAGACATTCACAGACATCTTCCTTTGT
  TGGTTTCCATTCTATTATGAACTAAAAATAGCATTTGTAGCCTGGCTGCTGTCTCCCTAC
  ACAAAAGGCTCCAGCCTCCTGTACAGGAAGTTTGTACATCCCACACTATCTTCAAAAGAA
  AAGGAAATCGATGATTGTCTGGTCCAAGCAAAAGACCGAAGTTACGATGCCCTTGTGCAC
  TTCGGGAAGCGGGGCTTGAACGTGGCCGCCACAGCGGCTGTGATGGCTGCTTCCAAGGGA
  CAGGGTGCCTTATCGGAGAGACTGCGGAGCTTCAGCATGCAGGACCTCACCACCATCAGG
  GGAGACGGCGCCCCTGCTCCCTCGGGCCCCCCACCACCGGGGTCTGGGCGGGCCAGCGGC
  AAACACGGCCAGCCTAAGATGTCCAGGAGTGCTTCTGAGAGCGCTAGCAGCTCAGGCACC
  GCCTAG
  
  Clone variation with respect to NM_022912.2
  285 g=>a
  5' Read Nucleotide Sequence

  >OriGene 5' read for NM_022912 unedited
  AATTTGTAATACGACTCACTATAGGGCGGCCGCGAATTCGGCACGAGGGAACGCCGCAGC
  AGCCCGCGCCGCCCGCAGCCTAGCCGAGCCGCGCCGCCCGGGCCTCGCCCGCCCGCCTGC
  CCGCCATGGTGTCATGGATCATCTCCAGGCTGGTGGTGCTTATATTTGGCACCCTTTACC
  CTGCGTATTATTCCTACAAGGCTGTGAAATCAAAGGACATTAAGGAATATGTCAAATGGA
  TGATGTACTGGATTATATTTGCACTTTTCACCACAGCAGAGACATTCACAGACATCTTCC
  TTTGTTGGTTTCCATTCTATTATGAACTAAAAATAGCATTTGTAGCCTGGCTGCTGTCTC
  CCTACACAAAAGGCTCCAGCCTCCTGTACAGGAAGTTTGTACATCCCACACTATCTTCAA
  AAGAAAAGGAAATCGATGATTGTCTGGTCCAAGCAAAAGACCGAAGTTACGATGCCCTTG
  TGCACTTCGGGAAGCGGGGCTTGAACGTGGCCGCCACAGCGGCTGTGATGGCTGCTTCCA
  AGGGACAGGGTGCCTTATCGGAGAGACTGCGGAGCTTCAGCATGCAGGACCTCACCACCA
  TCAGGGGAGACGGCGCCCCTGCTCCCTCGGGCCCCCCAACCACCGGGGTCTGGCGGGCCA
  GCGGCAAACACGGCCAGCCTAAGATGTCCAGGAGTGCTTCTGAGAGCGCTAGCAGCTCAN
  GCACCGNNCTAAATCCTTCGATCTCGCTTCAGGAAGAAAATACCTCATCCTCGGCCACCG
  AAACCCCGTGAGTGAGATGAGCCAACAGCACCGGATCCACANATAGTTTCTTCTCTGCCT
  TAAGAGCTATTCACTATACATANAATCGCAGCCTGGTGTCTTTGGATGTGCAACT
  
  3' Read Nucleotide Sequence

  >OriGene 3' read for NM_022912 unedited
  CCGCGGGCCGCAATCTANAGTCGAGTTTTTTTTTTTTTTTTTTTGCATTCGTTTCTGATA
  ATTCTGGGTACTTCCAACTAACAGGTAAATACATTTTAAAGAGTATATTCTTCTTCTGTC
  TGGAACTACTCAATGAGCACAAAGAAAACATTTTCTGTCTTCCTTAACAGATTTAGGTAT
  TGGTGGGTGTGGGGCACAGAACATGAGCAAACAGCTTCTGTTTATCCTCTCAGCCACAAA
  TTCGCTTTTAGGTATATTTTCCTATACCCTTTTGCAAATTACAAAATCACCTTCAGAGGA
  ACTATGGGTAGATGGGATTCCAATATGCATATCTGGCAACAATCAGCTTCAAATCAAACC
  CTTTCTGGGGTGGCTAAGATCCAGCTAATGTGTCATCAGCAAAGGCCTCTAATATGTGTT
  TGCGTAGTAATGGAACAGTTTTTAATTGGGCCTGTTTATAGTTGACTGACAGTAAGTTCT
  ATATGGTATATAACACTAATTCTCTAGTCTTCTGGGCATATCTACGAACAAATACAATCC
  AAATATTATGAGTAACTGGGTTGTGACCACTGCATGCATTACACTGAAAGAAACACCAAC
  TCGAAGCACAAATATATTATTCTTATATTTCGGCTCAGCTCTCAGTGGGGAGAGCAGCTA
  CCTCGGGACCACATGCCATTTAAACCAGATTCTTTTCAAATAAAATTCTCAATCTAAGTG
  GAAAGCCCCCTCAGAGGATGCCCTTATCCCCTACTAACAATCCAGGCTTGATAAAACGTC
  TGATAGGCCTGTAGTGCCCATGAGTATGAGTCTGCTGTTTCATTCTGCACAGCCAAGAGG
  GGACAGAAGTGTGAGCCCAGGTGCTCCTGGGTCTGACCAACAGTCTAACCATGAAAACTT
  CAGCCTCCAACCATTCTAGACCCACCATTTGATTGTACCT
  
• Restriction Sites: NotI-NotI
• ACCN: NM_022912
• ORF Size: 606 bp
• Insert Size: 2820
• 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_022912.1, NP_075063.1
• RefSeq Size: 3856
• RefSeq ORF: 606
• Locus ID: 65055
• Domains: TB2_DP1_HVA22
• Protein Families: Druggable Genome, Transmembrane
• Gene Summary: This gene encodes a mitochondrial protein that functions to enhance the cell surface expression of odorant receptors. Mutations in this gene cause spastic paraplegia autosomal dominant type 31, a neurodegenerative disorder. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Sep 2009]
  Transcript Variant: This variant (2) differs in the 5' UTR and 5' coding region, compared to variant 1. The encoded isoform (2) has a distinct and shorter N-terminus, compared to isoform 1.