WBSCR22 (AK091162) Human Untagged Clone
CAT#: SC312314
(untagged)-Human cDNA FLJ33843 fis, clone CTONG2005110, moderately similar to PUTATIVE METHYLTRANSFERASE (EC 2.1.1.-)
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Specifications
Product Data | |
Type | Human Untagged Clone |
Tag | Tag Free |
Symbol | WBSCR22 |
Synonyms | HASJ4442|HUSSY-3|MERM1|PP3381|WBMT |
Vector | pCMV6 series |
Sequence Data |
>NCBI ORF sequence for AK091162, the custom clone sequence may differ by one or more nucleotides
|
Restriction Sites | Please inquire |
ACCN | AK091162 |
ORF Size | 2496 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 | AK091162.1, BAG52295.1 |
RefSeq Size | 2496 |
RefSeq ORF | 2496 |
Locus ID | 114049 |
Protein Families | Druggable Genome |
Protein Pathways | Androgen and estrogen metabolism, Histidine metabolism, Selenoamino acid metabolism, Tyrosine metabolism |
Gene Summary | This gene encodes a protein containing a nuclear localization signal and an S-adenosyl-L-methionine binding motif typical of methyltransferases, suggesting that the encoded protein may act on DNA methylation. This gene is deleted in Williams syndrome, a multisystem developmental disorder caused by the deletion of contiguous genes at 7q11.23. Alternatively spliced transcript variants have been found. [provided by RefSeq, Feb 2011] |
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