Cd247 (NM_170789) Rat Untagged Clone

CAT#: RN208401

Cd247 (untagged ORF) - Rat Cd247 molecule (Cd247), (10 ug)

Specifications

Product Data

• Type: Rat Untagged Clone
• Tag: Tag Free
• Symbol: Cd247
• Synonyms: Cd3z; TCRzeta
• Vector: pCMV6-Entry
• E. coli Selection: Kanamycin (25 ug/mL)
• Mammalian Cell Selection: Neomycin
• Sequence Data:
  Fully Sequenced ORF

  >RN208401 representing NM_170789
  Red=Cloning site Blue=ORF Orange=Stop codon
  
  TTTTGTAATACGACTCACTATAGGGCGGCCGGGAATTCGTCGACTGGATCCGGTACCGAGGAGATCTGCC
  GCCGCGATCGCC
  
  ATGAAGTGGACGGCATCAGTCCTCGCCTGCATCCTTCAAGTGCAGTTCCCAGGAGCAGAGGCACAGAGCT
  TTGGTCTGCTGGATCCCAAACTCTGCTATATGCTAGATGGAATCCTCTTCATCTACGGAGTCATCGTCAC
  GGCCCTGTACCTGAGAGCAAAATTCAGCAGGAGTGCAGATGCTGCTGCTTACCTTCAGGACCCCAACCAG
  CTCTATAACGAGCTCAACCTAGGGCGAAGAGAGGAATATGATGTTTTGGACAAGAAGCGGCCTCGGGATC
  CGGAGATGGGGGGCAAACAGCAGAGGAGGAGGAACCCCCAGGAAGGCGTGTACAATGCACTGCAGAAAGA
  CAAGATGGCAGAGGCCTACAGTGAGATTGGCATGAAAGGCGAGAGGCGGAGAGGCAAGGGGCACGACGGC
  CTTTACCAGGGTCTCAGCACTGCCACCAAGGACACCTATGACGCCCTGCATATGCAGACCCTGCCCCCTC
  GCTAA
  
  ACGCGTACGCGGCCGCTCGAGCAGAAACTCATCTCAGAAGAGGATCTGGCAGCAAATGATATCCTGGATT
  ACAAGGATGACGACGATAAGGTTTAA
• Restriction Sites: SgfI-MluI
• ACCN: NM_170789
• ORF Size: 495 bp
• Insert Size: 495
• 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_170789.2, NP_740770.2
• RefSeq Size: 1741
• RefSeq ORF: 495
• Locus ID: 25300
• Gene Summary: component of T cell receptor (TCR) complex that plays a role in TCR assembly and signaling; does not promote surface expression of Fc gamma RIII, unlike human homolog [RGD, Feb 2006]
  Transcript Variant: This variant (1) encodes the longer isoform (1). 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.