CRIPT (NM_014171) Human Tagged ORF Clone

CAT#: RG204980

CRIPT (GFP-tagged) - Human cysteine-rich PDZ-binding protein (CRIPT)

Specifications

Product Data

• Type: Human Tagged ORF Clone
• Tag: TurboGFP
• Symbol: CRIPT
• Synonyms: HSPC139; SSMDF
• Vector: pCMV6-AC-GFP
• E. coli Selection: Ampicillin (100 ug/mL)
• Mammalian Cell Selection: Neomycin
• Sequence Data:
  ORF Nucleotide Sequence

  >RG204980 representing NM_014171
  Red=Cloning site Blue=ORF Green=Tags(s)
  
  TTTTGTAATACGACTCACTATAGGGCGGCCGGGAATTCGTCGACTGGATCCGGTACCGAGGAGATCTGCC
  GCCGCGATCGCC
  
  ATGGTGTGCGAAAAATGTGAAAAGAAACTTGGTACTGTTATCACTCCAGATACATGGAAAGATGGTGCTA
  GGAATACCACAGAAAGTGGTGGAAGAAAGCTGAATGAAAATAAAGCTTTGACTTCAAAAAAAGCAAGATT
  TGATCCATATGGAAAGAATAAGTTCTCCACTTGTAGAATTTGTAAAAGTTCTGTGCACCAACCAGGTTCT
  CATTACTGCCAGGGCTGTGCCTACAAAAAAGGCATCTGTGCGATGTGTGGAAAAAAGGTTTTGGATACCA
  AAAACTACAAGCAAACATCTGTC
  
  ACGCGTACGCGGCCGCTCGAG - GFP Tag - GTTTAA
  Protein Sequence

  >RG204980 representing NM_014171
  Red=Cloning site Green=Tags(s)
  
  MVCEKCEKKLGTVITPDTWKDGARNTTESGGRKLNENKALTSKKARFDPYGKNKFSTCRICKSSVHQPGS
  HYCQGCAYKKGICAMCGKKVLDTKNYKQTSV
  
  TRTRRLE - GFP Tag - V
• Restriction Sites: SgfI-MluI Cloning Scheme for this gene Plasmid Map
• ACCN: NM_014171
• ORF Size: 303 bp
• OTI Disclaimer: The molecular sequence of this clone aligns with the gene accession number as a point of reference only. However, individual transcript sequences of the same gene can differ through naturally occurring variations (e.g. polymorphisms), each with its own valid existence. This clone is substantially in agreement with the reference, but a complete review of all prevailing variants is recommended prior to use. More info
• OTI Annotation: This clone was engineered to express the complete ORF with an expression tag. Expression varies depending on the nature of the gene.

Reference Data

• RefSeq: NM_014171.3, NP_054890.1
• RefSeq Size: 1255
• RefSeq ORF: 306
• Locus ID: 9419
• Gene Summary: This gene encodes a protein that binds to the PDZ3 peptide recognition domain. The encoded protein may modulates protein interactions with the cytoskeleton. A mutation in this gene resulted in short stature with microcephaly and distinctive facies. [provided by RefSeq, Jun 2014]