ABHD11 (NM_031295) Human Untagged Clone

CAT#: SC110667

ABHD11 (untagged)-Human abhydrolase domain containing 11 (ABHD11), transcript variant 4

Specifications

Product Data

• Type: Human Untagged Clone
• Tag: Tag Free
• Symbol: ABHD11
• Synonyms: abhydrolase domain containing 11; PP1226; PP1226, WBSCR21; WBSCR21; Williams Beuren syndrome chromosome region 21
• Vector: pCMV6-XL5
• E. coli Selection: Ampicillin (100 ug/mL)
• Mammalian Cell Selection: None
• Sequence Data:
  Fully Sequenced ORF

  >NCBI ORF sequence for NM_031295, the custom clone sequence may differ by one or more nucleotides
  
  
  ATGCGAGCCGGCCAACAGCTTGCAAGCATGCTCCGCTGGACCCGAGCCTGGAGGCTCCCGCGTGAGGGAC
  TCGGCCCCCACGGCCCTAGCTTCGCGAGGGTGCCTGTCGCACCCAGCAGCAGCAGCGGCGGCCGAGGGGG
  CGCCGAGCCGAGGCCGCTTCCGCTTTCCTACAGGCTTCTGGACGGGGAGGCAGCCCTCCCGGCCGTCGTC
  TTTTTGCACGGGCTCTTCGGCAGCAAAACTAACTTCAACTCCATCGCCAAGATCTTGGCCCAGCAGACAG
  GCCGTGCTGACGGTGGATGCTCGTAA
  
  
  5' Read Nucleotide Sequence

  >OriGene 5' read for NM_031295 unedited
  GTCACATTTGTATACGACTCACTATAGGCGGCCGCGATTCGGCACGAGGGTGAGATGCGA
  GCCGGCCAACAGCTTGCAAGCATGCTCCGCTGGACCCGAGCCTGGAGGCTCCCGCGTGAG
  GGACTCGGCCCCCACGGCCCTAGCTTCGCGAGGGTGCCTGTCGCACCCAGCAGCAGCAGC
  GGCGGCCGAGGGGGCGCCGAGCCGAGGCCGCTTCCGCTTTCCTACAGGCTTCTGGACGGG
  GAGGCAGCCCTCCCGGCCGTCGTCTTTTTGCACGGGCTCTTCGGCAGCAAAACTAACTTC
  AACTCCATCGCCAAGATCTTGGCCCAGCAGACAGGCCGTAGGGTGCTGACGGTGGATGCT
  CGTAACCACGGTGACAGCCCCCACAGCCCAGACATGAGCTACGAGATCATGAGCCAGGAC
  CTGCAGGACCTTCTGCCCCAGCTGGGCCTGGTGCCCTGCGTCGTCGTTGGCCACAGCATG
  GGAGGAAAGACAGCCATGCTGCTGGCACTACAGAGGCCAGAGCTGGTGGAACGTCTCATT
  GCTGTAGATATCAGCCCAGTGGAAAGCACAGGTGTCTCCCACTTTGCAACCTATGTGGCA
  GCCATGAGGGCCATCAACATCGCAGATGAGCTGCCCCGCTCCCGTGCCCGAAAACTGGCG
  GATGAACAGCTCAGTTCTGTCATCCAGGACATGGCCGTGCGGCAGCACCTGCTCACTAAC
  CTGGTAGAGGTAGACGGGCGCCTTCTGTGGAGGGTGAACTTGGATGCCCTGACCCAGCAC
  CTAGACAAGATCTTGCTTTTCCCACAAAGCAGGAGTCCTACCCGGGGCCACACTTTTTCT
  CCTTGTTGGAACCTCCAGTTTGGGCCTTCCACCCCAACCTGGAATATGCGGCTCTTCCCC
  GG
  
  3' Read Nucleotide Sequence

  >OriGene 3' read for NM_031295 unedited
  GCTATGGACCGCGGCACGCAATCTAGGATCGAGTTTTTTTTTTTTTTTTTTCCAGCTAAT
  TTTTGTATTTTTAGTAAAGAAGGGTTTCACCATGTTGGCCAGGCTGGTCTCCAACTCCTG
  GCCTCAAGTCATCCTCCCGCCTTATCCTCCCAAAGTGCTGGAATTACAGGCATGAGCCAC
  CACGCCCGGCCATCTTCTTGCCAGCAACTCTTATACCAGGAAGCCTCGGATGGCAGCTAT
  GAAGCCCTGTGGGCGGTCAGCGTGGATCCAGTGGCCAGCGTTCGGCACCGTCTGCATCTG
  GGCCCGAGGGAAGAGCCGCATAATCTCAGGGGGGTGGCTGGGATGCACGAACTGGGAGTT
  TCCACCAAGGAGAAAGAGTGTTGGCCCGAGGTAGGACTCCTGCCTCTGTGGGAAAGCCAA
  GATCTTGCCTAGGCGCTGGGCCAGGGCATCCAAGTTCACCCTCCACACGAAGCGCCCGTC
  TACCTCTACCAGGTTAGGGAGCAGGTGCTGCCGCACGCCCATGTCCTGAATGACAGACCT
  GACCTGTCCATCCGCAGTTTTCGGGCCCGGAACCGGGGCACCTATCTGCGATGTGGAGGC
  CCCCATGGCTGCCCCAAGGCTCGAAAGTGGGAAAACCTGGGCCTTCCACTGGGCTGATAT
  CAACACATGGAAACCTTCCACCAGCTCGGCCCTTGGAGGCCAACAACAAGGCTGCTTTTC
  CTCCAAGCGTGCGCCCACGACAACCAAGGCCCCAGGCCAATTGGGGCAAAGGGCCCGCAG
  GCCCTGGCCTATGACCCCAAATCAAGCCCGGCCGGGGGGCCGACACCGGGGTACAAACTT
  CCCCGTAGAACCCTCAGCGCGGTCGTGGGGCCAAACTTGACAAGGAGTAAAATATCTCGC
  CGCACAACCCCACCAAAAAACCGCTCGGCGCCCACCCTCCCCCAACCGGTGGAN
  
• Restriction Sites: NotI-NotI
• ACCN: NM_031295
• ORF Size: 1632 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).

Reference Data

• RefSeq: NM_031295.3, NP_112585.2
• RefSeq Size: 1667
• RefSeq ORF: 1632
• Locus ID: 83451
• Gene Summary: This gene encodes a protein containing an alpha/beta hydrolase fold domain. This gene is deleted in Williams syndrome, a multisystem developmental disorder caused by the deletion of contiguous genes at 7q11.23. [provided by RefSeq, Mar 2016]
  Transcript Variant: This variant (4) contains an alternate segment in the 3' UTR, and lacks a short segment in the coding region, which causes a frameshift, as compared to variant 1. It encodes a much shorter isoform (4), also known as form B, than isoform 1.