ABHD11 (NM_148912) Human Untagged Clone

CAT#: SC124274

ABHD11 (untagged)-Human abhydrolase domain containing 11 (ABHD11), nuclear gene encoding mitochondrial protein, transcript variant 1

Specifications

Product Data

• Type: Human Untagged Clone
• Tag: Tag Free
• Symbol: ABHD11
• Synonyms: PP1226; WBSCR21
• Vector: pCMV6-XL5
• E. coli Selection: Ampicillin (100 ug/mL)
• Mammalian Cell Selection: None
• Sequence Data:
  Fully Sequenced ORF

  >NCBI ORF sequence for NM_148912, the custom clone sequence may differ by one or more nucleotides
  
  
  ATGCGAGCCGGCCAACAGCTTGCAAGCATGCTCCGCTGGACCCGAGCCTGGAGGCTCCCGCGTGAGGGAC
  TCGGCCCCCACGGCCCTAGCTTCGCGAGGGTGCCTGTCGCACCCAGCAGCAGCAGCGGCGGCCGAGGGGG
  CGCCGAGCCGAGGCCGCTTCCGCTTTCCTACAGGCTTCTGGACGGGGAGGCAGCCCTCCCGGCCGTCGTC
  TTTTTGCACGGGCTCTTCGGCAGCAAAACTAACTTCAACTCCATCGCCAAGATCTTGGCCCAGCAGACAG
  GCCGTAGGGTGCTGACGGTGGATGCTCGTAACCACGGTGACAGCCCCCACAGCCCAGACATGAGCTACGA
  GATCATGAGCCAGGACCTGCAGGACCTTCTGCCCCAGCTGGGCCTGGTGCCCTGCGTCGTCGTTGGCCAC
  AGCATGGGAGGAAAGACAGCCATGCTGCTGGCACTACAGAGGCCAGAGCTGGTGGAACGTCTCATTGCTG
  TAGATATCAGCCCAGTGGAAAGCACAGGTGTCTCCCACTTTGCAACCTATGTGGCAGCCATGAGGGCCAT
  CAACATCGCAGATGAGCTGCCCCGCTCCCGTGCCCGAAAACTGGCGGATGAACAGCTCAGTTCTGTCATC
  CAGGACATGGCCGTGCGGCAGCACCTGCTCACTAACCTGGTAGAGGTAGACGGGCGCTTCGTGTGGAGGG
  TGAACTTGGATGCCCTGACCCAGCACCTAGACAAGATCTTGGCTTTCCCACAGAGGCAGGAGTCCTACCT
  CGGGCCAACACTCTTTCTCCTTGGTGGAAACTCCCAGTTCGTGCATCCCAGCCACCACCCTGAGATTATG
  CGGCTCTTCCCTCGGGCCCAGATGCAGACGGTGCCGAACGCTGGCCACTGGATCCACGCTGACCGCCCAC
  AGGACTTCATAGCTGCCATCCGAGGCTTCCTGGTCTAA
  
  
  5' Read Nucleotide Sequence

  >OriGene 5' read for NM_148912 unedited
  CCCCGTTCAGGATATTTGTATACGACTCACTATAGNNGGCGGCCGCGCAATTCGGCACGA
  GGCTGCGAGCTAGGGCGGGAGAAGGAGCGCGGGGAGGACGTACCTTGTGAGATGCGAGCC
  GGCCAACAGCTTGCAAGCATGCTCCGCTGGACCCGAGCCTGGAGGCTCCCGCGTGAGGGA
  CTCGGCCCCCACGGCCCTAGCTTCGCGAGGGTGCCTGTCGCACCCAGCAGCAGCAGCGGC
  GGCCGAGGGGGCGCCGAGCCGAGGCCGCTTCCGCTTTCCTACAGGCTTCTGGACGGGGAG
  GCAGCCCTCCCGGCCGTCGTCTTTTTGCACGGGCTCTTCGGCAGCAAAACTAACTTCAAC
  TCCATCGCCAAGATCTTGGCCCAGCAGACAGGCCGTAGGGTGCTGACGGTGGATGCTCGT
  AACCACGGTGACAGCCCCCACAGCCCAGACATGAGCTACGAGATCATGAGCCAGGACCTG
  CAGGACCTTCTGCCCCAGCTGGGCCTGGTGCCCTGCGTCGTCGTTGGCCACAGCATGGGA
  GGAAAGACAGCCATGCTGCTGGCACTACAGAGGGTGAGCCGCCCATGTCTGGNGCCTCCT
  CCCATTCACTATATACCCTGANGGCCCTGCAGGCAACCTGNGACTCACATGATCGTTGGA
  TGACCAAGTTCAGGCTCCAGNAGCCATGCCTGAGACTCCCTATGTCTGCCTAAGACTGGT
  CCCAGTTCCGTTCTCTCCCACAGCCAGAGCTGGTGGAACGTCTCATTGCTGTAGAATCAG
  CCCAGTGGAAGCACAGTGTCTCCCACTTGCACCCACGTTGCAGCCATGAGCCCACTAACT
  CGCAGAGACCTGCCCGCTCCCGTGCCCGAAACTGGCGGATGACCAGTCATTCTGCATCCA
  GAACTGGCCGGCCGCAGC
  
• Restriction Sites: ECoRI-NOT
• ACCN: NM_148912
• ORF Size: 948 bp
• Insert Size: 4700
• OTI Disclaimer: Due to the inherent nature of this plasmid, standard methods to replicate additional amounts of DNA in E. coli are highly likely to result in mutations and/or rearrangements. Therefore, OriGene does not guarantee the capability to replicate this plasmid DNA. Additional amounts of DNA can be purchased from OriGene with batch-specific, full-sequence verification at a reduced cost. Please contact our customer care team at custsupport@origene.com or by calling 301.340.3188 option 3 for pricing and delivery.
  
  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

Reference Data

• RefSeq: NM_148912.2, NP_683710.1
• RefSeq Size: 1467
• RefSeq ORF: 948
• 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 (1, also known as A) encodes the longest isoform (1).