ELMO2 (NM_182764) Human Untagged Clone

CAT#: SC314534

ELMO2 (untagged)-Human engulfment and cell motility 2 (ELMO2), transcript variant 2

Specifications

Product Data

• Type: Human Untagged Clone
• Tag: Tag Free
• Symbol: ELMO2
• Synonyms: CED-12; Ced-12A; CED12; ELMO-2; VMPI
• Vector: pCMV6-Entry
• E. coli Selection: Kanamycin (25 ug/mL)
• Mammalian Cell Selection: Neomycin
• Sequence Data:
  Fully Sequenced ORF

  >NCBI ORF sequence for NM_182764, the custom clone sequence may differ by one or more nucleotides
  
  
  ATGCCACCACCGTCAGACATTGTCAAAGTGGCCATTGAGTGGCCAGGTGCTAACGCCCAGCTCCTTGAAA
  TCGACCAGAAACGGCCCCTGGCATCCATTATCAAGGAAGTTTGTGATGGGTGGTCGTTGCCAAACCCAGA
  GTATTATACCCTCCGTTATGCAGATGGTCCTCAGCTGTACATCACCGAACAGACTCGCAGTGACATTAAG
  AATGGGACAATCTTACAACTGGCTATCTCCCCGTCCCGGGCTGCACGCCAGCTGATGGAGAGGACCCAGT
  CATCCAACATGGAGACCCGGCTGGATGCCATGAAGGAGCTGGCCAAGCTCTCTGCCGACGTGACTTTCGC
  TACTGAGTTCATCAACATGGATGGCATCATTGTGCTGACAAGGCTCGTGGAAAGTGGAACCAAGCTCTTG
  TCCCACTACAGTGAGATGCTGGCATTCACCCTGACTGCCTTCCTAGAGCTCATGGACCATGGCATTGTCT
  CCTGGGACATGGTTTCAATCACCTTTATTAAGCAGATTGCAGGGTATGTGAGCCAGCCCATGGTGGACGT
  GTCAATCCTTCAGAGGTCCCTGGCCATCCTGGAGAGCATGGTCTTGAACAGCCAGAGTCTGTACCAGAAG
  ATAGCCGAGGAAATCACCGTGGGACAGCTCATCTCACACCTCCAGGTCTCCAACCAGGAGATTCAGACCT
  ACGCCATTGCACTGATTAATGCACTTTTTCTGAAGGCTCCTGAGGACAAACGACAGGATATGGCAAATGC
  ATTTGCACAGAAGCATCTCCGGTCTATAATCCTGAATCATGTGATCCGAGGGAACCGCCCCATCAAAACT
  GAGATGGCCCATCAGCTATATGTCCTTCAAGTCCTAACCTTTAACCTTCTGGAAGAAAGGATGATGACCA
  AGATGGACCCCAATGACCAGGCTCAAAGGGACATCATATTTGAACTGAGGAGGATTGCATTTGACGCAGA
  GTCTGATCCTAGCAATGCCCCTGGGAGTGGGACCGAAAAACGCAAAGCCATGTACACAAAGGACTACAAA
  ATGCTGGGATTTACCAACCACATCAATCCAGCCATGGACTTTACCCAGACTCCTCCTGGAATGCTGGCCT
  TGGACAACATGCTGTACTTGGCTAAAGTCCACCAGGACACCTACATCCGGATTGTCTTGGAGAACAGTAG
  CCGGGAAGACAAACATGAATGCCCCTTTGGCCGCAGTGCCATTGAGCTCACCAAAATGCTCTGTGAAATC
  CTGCAGGTTGGGGAACTACCAAATGAAGGACGCAATGACTACCACCCGATGTTCTTTACCCATGACCGAG
  CCTTTGAAGAGCTCTTTGGAATCTGCATCCAGCTGTTGAACAAGACCTGGAAGGAGATGAGGGCAACAGC
  AGAGGACTTCAACAAGGTTATGCAAGTCGTCCGAGAGCAAATCACTCGAGCTTTGCCCTCCAAACCCAAC
  TCTTTGGATCAGTTCAAGAGCAAATTGCGTAGCCTGAGTTACTCTGAGATTCTACGACTGCGCCAGTCTG
  AGAGGATGAGTCAGGATGACTTCCAGTCCCCGCCAATTGTGGAGCTGAGGGAGAAGATCCAGCCCGAGAT
  CCTTGAGCTGATCAAGCAGCAGCGCCTGAACCGGCTCTGTGAGGGCAGCAGCTTCCGAAAGATTGGGAAC
  CGCCGAAGGCAAGAACGGTTCTGGTACTGCCGGTTGGCACTGAACCACAAGGTCCTTCACTATGGTGACT
  TGGATGACAACCCACAAGGGGAGGTGACATTTGAATCCCTGCAGGAGAAAATTCCTGTTGCAGACATTAA
  GGCCATTGTCACTGGGAAAGATTGTCCCCACATGAAAGAGAAAAGTGCTCTGAAACAGAACAAGGAGGTG
  TTGGAATTGGCCTTCTCCATCCTGTATGACCCTGATGAGACCTTAAACTTCATCGCACCTAATAAATATG
  AGTACTGCATCTGGATTGATGGCCTCAGTGCCCTTCTGGGGAAGGACATGTCCAGTGAGCTGACCAAGAG
  TGACCTGGACACCCTGCTGAGCATGGAGATGAAGCTGCGGCTCCTGGACCTGGAGAACATCCAGATTCCC
  GAAGCCCCACCCCCCATCCCCAAGGAGCCCAGCAGCTATGACTTTGTCTATCACTATGGCTGA
  
  
• Restriction Sites: SgfI-MluI
• ACCN: NM_182764
• ORF Size: 2163 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).
• OTI Annotation: This TrueClone is provided through our Custom Cloning Process that includes sub-cloning into OriGene's pCMV6 vector and full sequencing to provide a non-variant match to the expected reference without frameshifts, and is delivered as lyophilized plasmid DNA.

Reference Data

• RefSeq: NM_182764.2, NP_877496.1
• RefSeq Size: 4021
• RefSeq ORF: 2163
• Locus ID: 63916
• Gene Summary: The protein encoded by this gene interacts with the dedicator of cyto-kinesis 1 protein. Similarity to a C. elegans protein suggests that this protein may function in phagocytosis of apoptotic cells and in cell migration. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Dec 2015]
  Transcript Variant: This variant (2) differs in the 5' UTR compared to variant 1. Variants 1 and 2 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.