ABHD11 (NM_031295) Human Untagged Clone

CAT#: SC110667

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


Reconstitution Protocol

USD 506.00

In Stock*

Size
    • 10 ug

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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
>NCBI ORF sequence for NM_031295, the custom clone sequence may differ by one or more nucleotides


ATGCGAGCCGGCCAACAGCTTGCAAGCATGCTCCGCTGGACCCGAGCCTGGAGGCTCCCGCGTGAGGGAC
TCGGCCCCCACGGCCCTAGCTTCGCGAGGGTGCCTGTCGCACCCAGCAGCAGCAGCGGCGGCCGAGGGGG
CGCCGAGCCGAGGCCGCTTCCGCTTTCCTACAGGCTTCTGGACGGGGAGGCAGCCCTCCCGGCCGTCGTC
TTTTTGCACGGGCTCTTCGGCAGCAAAACTAACTTCAACTCCATCGCCAAGATCTTGGCCCAGCAGACAG
GCCGTGCTGACGGTGGATGCTCGTAA


>OriGene 5' read for NM_031295 unedited
GTCACATTTGTATACGACTCACTATAGGCGGCCGCGATTCGGCACGAGGGTGAGATGCGA
GCCGGCCAACAGCTTGCAAGCATGCTCCGCTGGACCCGAGCCTGGAGGCTCCCGCGTGAG
GGACTCGGCCCCCACGGCCCTAGCTTCGCGAGGGTGCCTGTCGCACCCAGCAGCAGCAGC
GGCGGCCGAGGGGGCGCCGAGCCGAGGCCGCTTCCGCTTTCCTACAGGCTTCTGGACGGG
GAGGCAGCCCTCCCGGCCGTCGTCTTTTTGCACGGGCTCTTCGGCAGCAAAACTAACTTC
AACTCCATCGCCAAGATCTTGGCCCAGCAGACAGGCCGTAGGGTGCTGACGGTGGATGCT
CGTAACCACGGTGACAGCCCCCACAGCCCAGACATGAGCTACGAGATCATGAGCCAGGAC
CTGCAGGACCTTCTGCCCCAGCTGGGCCTGGTGCCCTGCGTCGTCGTTGGCCACAGCATG
GGAGGAAAGACAGCCATGCTGCTGGCACTACAGAGGCCAGAGCTGGTGGAACGTCTCATT
GCTGTAGATATCAGCCCAGTGGAAAGCACAGGTGTCTCCCACTTTGCAACCTATGTGGCA
GCCATGAGGGCCATCAACATCGCAGATGAGCTGCCCCGCTCCCGTGCCCGAAAACTGGCG
GATGAACAGCTCAGTTCTGTCATCCAGGACATGGCCGTGCGGCAGCACCTGCTCACTAAC
CTGGTAGAGGTAGACGGGCGCCTTCTGTGGAGGGTGAACTTGGATGCCCTGACCCAGCAC
CTAGACAAGATCTTGCTTTTCCCACAAAGCAGGAGTCCTACCCGGGGCCACACTTTTTCT
CCTTGTTGGAACCTCCAGTTTGGGCCTTCCACCCCAACCTGGAATATGCGGCTCTTCCCC
GG
>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
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).
Product Components The ORF clone is ion-exchange column purified and shipped in a 2D barcoded Matrix tube containing 10ug of transfection-ready, dried plasmid DNA (reconstitute with 100 ul of water).
Reconstitution 1. Centrifuge at 5,000xg for 5min.
2. Carefully open the tube and add 100ul of sterile water to dissolve the DNA.
3. Close the tube and incubate for 10 minutes at room temperature.
4. Briefly vortex the tube and then do a quick spin (less than 5000xg) to concentrate the liquid at the bottom.
5. Store the suspended plasmid at -20°C. The DNA is stable for at least one year from date of shipping when stored at -20°C.
Reference Data
RefSeq NM_031295.3, NP_112585.2
RefSeq Size 1667 bp
RefSeq ORF 1632 bp
Locus ID 83451
Cytogenetics 7q11.23
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.

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