RIM1 (RIMS1) (NM_001168408) Human Untagged Clone

CAT#: SC329151

RIMS1 (untagged)-Human regulating synaptic membrane exocytosis 1 (RIMS1) transcript variant 3

Specifications

Product Data

• Type: Human Untagged Clone
• Tag: Tag Free
• Symbol: RIMS1
• Synonyms: CORD7; RAB3IP2; RIM; RIM1
• Vector: pCMV6-XL5
• E. coli Selection: Ampicillin (100 ug/mL)
• Mammalian Cell Selection: None
• Sequence Data:
  Fully Sequenced ORF

  >NCBI ORF sequence for NM_001168408, the custom clone sequence may differ by one or more nucleotides
  ATGTGTGCACCTGGGATTCATGTCTCTTCAGAAGGGTGGGAAGAAGTGAGGTCTGTTGAT
  TCCGAAGAGGGAACAATTGAAGCTCGACGAGCAGTTGCTGGTGATTTGGATTATTACTGG
  TTGGATCCTGCCACGTGGCACAGCCGGGAGACATCACCTATTAGTTCGCATCCTGTAACG
  TGGCAACCATCTAAAGAGGGGGACCGATTAATTGGACGTGTTATTCTTAACAAGAGAACA
  ACCATGCCCAAAGACTCAGGTGCATTGCTGGGTCTGAAAGTTGTTGGAGGAAAAATGACT
  GACTTAGGACGACTTGGTGCTTTCATCACCAAAGTAAAGAAGGGTAGCCTAGCAGATGTA
  GTTGGACACCTAAGAGCAGGGGATGAAGTTCTAGAATGGAATGGTAAACCCCTGCCGGGA
  GCTACAAATGAAGAAGTTTACAACATTATTTTAGAATCAAAATCAGAACCTCAAGTTGAA
  ATTATTGTTTCAAGGCCTATTGGTGACATTCCCCGGATTCCTGAGAGCTCCCACCCTCCA
  CTGGAGTCCAGTTCAAGTTCCTTTGAATCTCAGAAGATGGAAAGGCCTTCCATTTCTGTT
  ATTTCTCCAACAAGTCCTGGAGCTCTAAAAGATGCCCCACAAGTCTTACCAGGGCAACTT
  TCTGTGAAGTTGTGGTATGATAAAGTGGGACACCAGCTGATTGTAAATGTTCTGCAAGCA
  ACAGATCTACCTGCTAGAGTAGATGGACGTCCTCGAAATCCCTATGTAAAAATGTATTTT
  CTTCCAGATAGAAGTGATAAAAGTAAAAGGAGGACCAAAACAGTAAAGAAAATACTAGAA
  CCAAAATGGAATCAAACTTTTGTCTATTCACATGTACATCGTAGAGATTTTAGAGAACGA
  ATGTTAGAAATAACTGTGTGGGACCAACCAAGAGTGCAAGAAGAAGAAAGTGAATTTCTT
  GGAGAGATCCTCATAGAATTGGAGACAGCGCTTTTAGATGATGAACCGCATTGGTATAAA
  CTTCAGACACATGATGAGTCTTCACTACCTCTGCCTCAGCCATCACCTTTCATGCCAAGG
  CGACATATTCATGGAGAAAGCTCTAGCAAAAAGCTACAAAGATCTCAGCGAATCAGTGAT
  AGTGACATCTCAGATTATGAGGTTGATGATGGTATTGGCGTAGTTCCTCCAGTAGGCTAT
  AGGTCTAGTGCTAGAGAAAGTAAATCTACAACATTAACTGTGCCAGAACAGCAAAGAACA
  ACTCATCACCGCTCACGTTCAGTATCTCCTCATCGCGGCAATGATCAGGGAAAGCCGCGT
  TCACGTTTACCAAATGTGCCATTACAGAGGAGTTTAGATGAAATTCATCCAACAAGAAGG
  TCACGTTCTCCAACCAGACACCATGATGCCTCCCGAAGTCCAGTTGATCATAGAACCAGA
  GATGTGGATAGTCAGTATTTATCAGAACAAGACAGTGAGCTTCTTATGCTGCCCAGAGCA
  AAACGAGGACGAAGTGCAGAATGCCTACATACTACCAGTGAACTGCAGCCCTTTCTTGAC
  AGGGCTAGGAGTGCTAGTACCAACTGCTTGAGACCAGATACTAGTTTGCATTCACCAGAA
  CGAGAAAGAATGCACCGACAGAGAAGTCCAACACAATCTCCTCCAGCAGACACATCGTTC
  AGCAGTCGCAGGGGAAGACAGCTCCCACAAGTGCCAGTGAGAAGCGGCAGTATAGAACAA
  GAGTCGGGCCACAAAAAGTTAAAAAGTACCATCCAGAGAAGCACAGAAACAGGCATGGCA
  GCTGAAATGAGAAAGATGGTAAGGCAGCCGAGCCGAGAGTCTACTGATGGCAGCATCAAC
  AGTTACAGCTCTGAGGGCAATTTAATATTTCCTGGAGTGCGACTGGGAGCTGACAGTCAA
  TTCAGTGATTTTCTTGATGGATTGGGACCAGCCCAGCTTGTTGGCCGCCAAACCCTTGCC
  ACCCCTGCAATGGGTGATATACAAATAGGAATGGAGGACAAAAAGGGCCAATTAGAAGTG
  GAAGTCATTAGAGCACGAAGCCTCACACAAAAGCCTGGTTCCAAATCTACACCTGCTCCA
  TATGTCAAAGTATATCTTTTGGAAAATGGGGCCTGTATAGCCAAGAAGAAGACAAGAATT
  GCACGAAAAACCCTTGATCCTTTGTATCAGCAGTCTCTGGTTTTTGATGAAAGTCCACAG
  GGTAAAGTTCTTCAGGTGATTGTCTGGGGAGACTATGGCAGAATGGACCACAAATGCTTT
  ATGGGTGTGGCTCAGATCTTGTTGGAAGAACTCGACCTGTCCAGCATGGTGATCGGATGG
  TACAAATTGTTCCCACCGTCCTCACTGGTGGATCCCACACTCACTCCCCTCACCCGGCGG
  GCTTCCCAGTCATCTCTGGAAAGTTCAACTGGGCCTCCCTGTATTCGATCATAG
  
• Restriction Sites: Please inquire
• ACCN: NM_001168408
• ORF Size: 2454 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_001168408.1, NP_001161880.1
• RefSeq Size: 5202
• RefSeq ORF: 2454
• Locus ID: 22999
• Gene Summary: The protein encoded by this gene is a RAS gene superfamily member that regulates synaptic vesicle exocytosis. This gene also plays a role in the regulation of voltage-gated calcium channels during neurotransmitter and insulin release. Mutations have suggested a role cognition and have been identified as the cause of cone-rod dystrophy type 7. Multiple transcript variants encoding different isoforms have been described for this gene. [provided by RefSeq, Mar 2012]
  Transcript Variant: This variant (3) differs in the 5' UTR and has multiple coding region differences, compared to variant 1. The resulting isoform (3) has a shorter and distinct N-terminus and internal differences, compared to isoform 1.