WBSCR22 (NM_017528) Human Untagged Clone
CAT#: SC320894
WBSCR22 (untagged)-Human Williams Beuren syndrome chromosome region 22 (WBSCR22), transcript variant 2
"NM_017528" in other vectors (5)
Product Images
![](https://cdn.origene.com/img/defaults-img-expression-plasmids.jpg)
Specifications
Product Data | |
Type | Human Untagged Clone |
Tag | Tag Free |
Symbol | WBSCR22 |
Synonyms | HASJ4442; HUSSY-3; MERM1; PP3381; WBMT; WBSCR22 |
Vector | pCMV6-AC |
E. coli Selection | Ampicillin (100 ug/mL) |
Mammalian Cell Selection | Neomycin |
Sequence Data |
>OriGene sequence for NM_017528.2
GTGCTGCTGAGGCGTGAGAATGGCGTCCCGCGGCCGGCGTCCGGAGCATGGCGGACCCCC
AGAGCTGTTTTATGACGAGACAGAAGCCCGGAAATACGTTCGCAACTCACGGATGATTGA TATCCAGACCAGGATGGCTGGGCGAGCATTGGAGCTTCTTTATCTGCCAGAGAATAAGCC CTGTTACCTGCTGGATATTGGCTGTGGCACTGGGCTGAGTGGAAGTTATCTGTCAGATGA AGGGCACTATTGGGTGGGCCTGGATATCAGCCCTGCCATGCTGGATGAGGCTGTGGACCG AGAGATAGAGGGAGACCTGCTGCTGGGGGATATGGGCCAGGGCATCCCATTCAAGCCAGG CACATTTGATGGTTGCATCAGCATTTCTGCTGTGCAGTGGCTCTGTAATGCTAACAAGAA GTCTGAAAACCCTGCCAAGCGCCTGTACTGCTTTTTTGCTTCTCTTTTTTCTGTTCTCGT CCGGGGATCCCGAGCTGTCCTGCAGCTGTACCCTGAGAACTCAGAGCAGTTGGAGCTGAT CACAACCCAGGCCACAAAGGCAGGCTTCTCCGGTGGCATGGTGGTAGACTACCCTAACAG TGCCAAAGCAAAGAAATTCTACCTCTGCTTGTTTTCTGGGCCTTCGACCTTTATACCAGA GGGGCTGAGTGAAAATCAGGATGAAGTTGAACCCAGGGAGTCTGTGTTCACCAATGAGAG GTTCCCATTAAGGATGTCGAGGCGGGGAATGGTGAGGAAGAGTCGGGCATGGGTGCTGGA GAAGAAGGAGCGGCACAGGCGCCAGGGCAGGGAAGTCAGACCTGACACCCAGTACACCGG CCGCAAGCGCAAGCCCCGCTTCTAAGTCACCACGCGGTTCTGGAAAGGCACTTGCCTCTG CACTTTTCTATATTGTTCAGCTGACAAAGTAGTATTTTAGAAAAGTTCTAAAGTTATAAA AATGTTTTCTGCAGTAAAAAAAAAGTTCTCTGGGCCGGGCGTGGTGGCTCACACCTGTAA TCCCAGCACCTTGGGAGGCTGAGGTGGGAGGATCATTTGAGGCCAGGAGTTTGAGACCTG CCTGGGCAACATAATGAAACTTCCTTTCCAGGGAGAAAAAAAAAAAAAAAAAAAAAAGCT CTGAGAGCATCTTATTTTGTTTAAAGGCAAGAAATAAAATTTCCTTTTGTGGAAAAAAAA AAAAAAAAAAAAAAAAAAAAA >OriGene 5' read for NM_017528.2 unedited
TCCATTGTATACGACTCCTATAGGGCGGCTCGGCTAATTCGGCACGCAGGGTGCTGCTGA GGCGTGAGAATGGCGTCCCGCGGCCGGCGTCCGGAGCATGGCGGACCCCCAGAGCTGTTT TATGACGAGACAGAAGCCCGGAAATACGTTCGCAACTCACGGATGATTGATATCCAGACC AGGATGGCTGGGCGAGCATTGGAGCTTCTTTATCTGCCAGAGAATAAGCCCTGTTACCTG CTGGATATTGGCTGTGGCACTGGGCTGAGTGGAAGTTATCTGTCAGATGAAGGGCACTAT TGGGTGGGCCTGGATATCAGCCCTTCCTTTCTGGATGAGGCTGTGGACCGAGAGATAGAG GGAGACCTGCTGCTGGGGGATATGGGCCAGGGCATCCCATTCAAGCCAGGCACATTTGAT GGTTGCATCAGCATTTCTGCTGTGCAGTGGCTCTGTAATGCTAACAAGAAGTCTGAAAAC CCTGCCAAGCGCCTGTACTGCTTTTTTGCTTCTCTTTTTTCTGTTCTCGTCCGGGGATCC CGAGCTGTCCTGCAGCTGTACCCTGAGAACTCAGAGCAGTTGGAGCTGATCACAACCCAG CCACAAAGGCAGGCTTCTCCGGTGGCATGGTGGTAGACTACCCTAACAGTGCCAAAGCAA AGAAATTCTACCTCTGCTTGTTTTCTGGGCCTTCGACCTTTATACCAGAGGGCTGAGTGA AAATCAGATGAAGTTGAACCCAGGGAGTCTGTGTTCACCAATGAGAGGTTCCCATTAAGA TGTCAAGCGGGAATGTGAGAAGAGTCAGCATGGGTGCTGGAGAAAAGACGCACAGCGCCA GGCAGGAAGTCAGACTGAACCCAGTACACGGCCGCAAGCCGCAGCCCGCTCCTAGTCACC ACGCGTTCTGAAGCATGCCTTGCCTTTTCTAATTGTTCAGCTGACAAGTTGAT |
Restriction Sites | Please inquire |
ACCN | NM_017528 |
ORF Size | 846 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_017528.2, NP_059998.2 |
RefSeq Size | 1258 |
RefSeq ORF | 846 |
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] Transcript Variant: This variant (2) lacks an exon in the 3' coding region but maintains the reading frame, compared to variant 1. The encoded isoform (2) is shorter than isoform 1. |
Documents
Product Manuals |
FAQs |
SDS |
Resources
Other Versions
SKU | Description | Size | Price |
---|---|---|---|
SC127812 | WBSCR22 (untagged)-Human Williams Beuren syndrome chromosome region 22 (WBSCR22), transcript variant 2 |
USD 310.00 |
|
RC204043 | WBSCR22 (Myc-DDK-tagged)-Human Williams Beuren syndrome chromosome region 22 (WBSCR22), transcript variant 2 |
USD 420.00 |
|
RG204043 | WBSCR22 (GFP-tagged) - Human Williams Beuren syndrome chromosome region 22 (WBSCR22), transcript variant 2 |
USD 460.00 |
|
RC204043L3 | Lenti ORF clone of Human Williams Beuren syndrome chromosome region 22 (WBSCR22), transcript variant 2, Myc-DDK-tagged |
USD 620.00 |
|
RC204043L4 | Lenti ORF clone of Human Williams Beuren syndrome chromosome region 22 (WBSCR22), transcript variant 2, mGFP tagged |
USD 620.00 |
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