PIAS1 (NM_016166) Human Untagged Clone

CAT#: SC114401

PIAS1 (untagged)-Human protein inhibitor of activated STAT, 1 (PIAS1)


  "NM_016166" in other vectors (6)

Reconstitution Protocol

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Size
    • 10 ug

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Specifications

Product Data
Type Human Untagged Clone
Tag Tag Free
Symbol PIAS1
Synonyms DDXBP1; GBP; GU/RH-II; ZMIZ3
Vector pCMV6-XL5
E. coli Selection Ampicillin (100 ug/mL)
Mammalian Cell Selection None
Sequence Data
>OriGene ORF within SC114401 sequence for NM_016166 edited (data generated by NextGen Sequencing)
ATGGCGGACAGTGCGGAACTAAAGCAAATGGTTATGAGCCTTAGAGTTTCTGAACTCCAA
GTACTGTTGGGCTACGCCGGGAGAAACAAGCACGGACGCAAACACGAACTTCTCACAAAA
GCCCTGCATTTGCTAAAGGCTGGCTGTAGTCCTGCTGTGCAAATGAAAATTAAGGAACTC
TATAGGCGGCGGTTCCCACAGAAAATCATGACGCCTGCAGACTTGTCCATCCCCAACGTA
CATTCAAGTCCTATGCCAGCAACTTTGTCTCCATCTACCATTCCACAACTCACTTACGAT
GGTCACCCTGCATCATCACCATTACTCCCTGTTTCTCTTCTGGGACCTAAACATGAACTG
GAACTCCCACATCTTACATCAGCTCTTCACCCAGTCCATCCGGATATAAAACTTCAAAAA
TTACCATTTTATGATTTACTGGATGAACTGATAAAACCCACCAGTCTAGCATCAGACAAC
AGTCAGCGCTTTCGAGAAACCTGTTTTGCATTTGCCTTGACACCACAACAAGTGCAGCAA
ATCAGTAGTTCCATGGATATTTCTGGGACCAAATGTGACTTCACAGTACAGGTCCAGTTA
AGGTTTTGTTTATCAGAAACCAGTTGTCCACAAGAAGATCACTTCCCACCCAATCTTTGT
GTGAAAGTGAATACAAAACCTTGCAGCCTTCCAGGTTACCTTCCACCTACAAAAAATGGC
GTGGAACCAAAGCGACCCAGCCGACCAATTAATATCACCTCACTTGTCCGACTGTCCACA
ACAGTACCAAACACGATTGTTGTTTCTTGGACTGCAGAAATTGGAAGAAACTATTCCATG
GCAGTATATCTTGTAAAACAGTTGTCCTCAACAGTTCTTCTTCAGAGGTTACGAGCAAAG
GGAATAAGGAATCCGGATCATTCTAGAGCTTTAATTAAAGAGAAGTTGACTGCGGATCCA
GACAGTGAAATAGCTACAACCAGCCTAAGGGTTTCTCTACTATGTCCACTTGGTAAAATG
CGGCTGACAATTCCGTGTCGGGCCCTTACATGTTCTCATCTACAATGTTTTGACGCAACT
CTTTACATTCAGATGAATGAGAAAAAACCAACCTGGGTTTGTCCTGTCTGTGATAAGAAG
GCTCCATATGAACACCTTATTATTGATGGCTTGTTTATGGAAATCCTAAAGTACTGTACA
GACTGTGATGAAATACAATTTAAGGAGGATGGCACTTGGGCACCGATGAGATCAAAAAAG
GAAGTACAGGAAGTTTCTGCCTCTTACAATGGAGTCGATGGATGCTTGAGCTCCACATTG
GAGCATCAGGTAGCGTCTCACCACCAGTCCTCAAATAAAAACAAGAAAGTAGAAGTGATT
GACCTAACCATAGACAGTTCATCTGATGAAGAGGAAGAAGAGCCATCTGCCAAGAGGACC
TGTCCTTCCCTATCTCCCACATCACCACTAAATAATAAAGGCATTTTAAGTCTTCCACAT
CAAGCATCTCCAGTATCCCGCACCCCAAGCCTTCCTGCTGTAGACACAAGCTACATTAAT
ACCTCCCTCATCCAAGACTATAGGCATCCTTTCCACATGACACCCATGCCTTACGACTTA
CAAGGATTAGATTTCTTTCCTTTCTTATCAGGAGACAATCAGCATTACAACACCTCCTTG
CTTGCCGCTGCAGCAGCAGCAGTTTCAGATGATCAAGACCTCCTACACTCGTCTCGGTTT
TTCCCGTATACCTCCTCACAGATGTTTCTTGATCAGTTAAGTGCAGGAGGCAGTACTTCT
CTGCCAACCACCAATGGAAGCAGTAGTGGCAGTAACAGCAGCCTGGTTTCTTCCAACAGC
CTAAGGGAAAGCCATAGCCACACCGTCACAAACAGGAGCAGCACGGACACGGCATCCATC
TTTGGCATCATACCAGACATTATTTCATTGGACTGA

Clone variation with respect to NM_016166.1
318 g=>a
>OriGene 5' read for NM_016166 unedited
TAATACGACTCACTATAGGGCGGCCGCGAATTCGGCACGAGGGCAAGATGGCGGACAGTG
CGGAACTAAAGCAAATGGTTATGAGCCTTAGAGTTTCTGAACTCCAAGTACTGTTGGGCT
ACGCCGGGAGAAACAAGCACGGACGCAAACACGAACTTCTCACAAAAGCCCTGCATTTGC
TAAAGGCTGGCTGTAGTCCTGCTGTGCAAATGAAAATTAAGGAACTCTATAGGCGGCGGT
TCCCACAGAAAATCATGACGCCTGCAGACTTGTCCATCCCCAACGTACATTCAAGTCCTA
TGCCAGCAACTTTGTCTCCATCTACCATTCCACAACTCACTTACGATGGTCACCCTGCAT
CATCACCATTACTCCCTGTTTCTCTTCTGGGACCTAAACATGAACTGGAACTCCCACATC
TTACATCAGCTCTTCACCCAGTCCATCCGGATATAAAACTTCAAAAATTACCATTTTATG
ATTTACTGGATGAACTGATAAAACCCACCAGTCTAGCATCAGACAACAGTCAGCGCTTTC
GAGAAACCTGTTTTGCATTTGCCTTGACACCACAACAAGTGCAGCAAATCAGTAGTTCCA
TGGATATTTCTGGGACCAAATGTGACTTCACAGTACAGGTCCAGTTAAGGGTTTTGTTTA
TCAGAAACCAGTTGTCCACAAGAAGATCACTTCCCACCCAATCTTTGTGTGAAAGTGAAT
ACAAAACCTTGCAGCCTTTNCAGGTTACCTTCCACCTACAAAAAAATGGCGTGGAACCAA
AGCGACCCAGCCGACCAATTAATATCACCTCACTTGTNCGACTGTCCACAACAGTACCCA
CACGAATTGTTGTTNCNTGGACTGCAGAAATGGAAGAAACTATTCATGGCAGTATATCTT
GTAAAACAGNTGTCCTCAACAGTTCTCTTTCAGAGGTACGGCAAAG
>OriGene 3' read for NM_016166 unedited
CGGCACGCAATCTAGAATCGAGTTTTTTTTTTTTTTTTTTCTTTCCTTTTTTTTTTTAAA
CAAGTGTTTTATCACACAGGCAGTCTTAAATTTATATACAAAAGTAAAACTGAAAATATA
GTTTTGTTCTCTGTACATTTCTTTTAATTTTTTCCCTAAAAAAAGGAAAAAAAACACGCT
TGTATACTTTTCTAAACAGAGTAAGGTAAAACAGAGCACAAAGTTCTCTTCTTTCTGCCA
AGTTCATTCGATCTGGGGTGGGGATGGGAGCAGCAGGGCCTGGGAATCAGTCCAATGAAA
TAATGTCTGGTATGATGCCAAAGATGGATGCCGTGTCCGTGCTGCTCCTGTTTGTGACGG
TGTGGCTATGGCTTTCCCTTAGGCTGTTGGAAGAAACCAGGCTGCTGTTACTGCCACTAC
TGCTTCCATTGGTGGTTGGCAGAGAAGTACTGCCTCCTGCACTTAACTGATCAAGAAACA
TCTGTGAGGAGGTATACGGGAAAAACCGAGACGAGTGTAGGAGGTCTTGATCATCTGAAA
CTGCTGCTGCTGCAGCGGCAAGCAAGGAGGTGTTGTAATGCTGATTGTCTCCTGATAAGA
AAGGAAAGAAATCTAATCCTTGTAAGTCGTAAGGCATGGGTGTCATGTGGAAAGGATGCC
TATAGTCTTGGATGAGGGAGGTATTAATGTACCTTGTGTCTACAGCAGGAAGGCTTGGGG
TGCGGNATACTGGAGATGCTTGATGTGGAAGACTTANAATGCCTTATTATTTANTGGTGA
TGTGGGAGATAGGAAAGACAGGTCCCTCTGGCAAATAGCTCCTCCTTCTCTTCATCANAT
GAACTGCCTATGGNTANGTCAATCACTTCTACTTTCCTGNTTTTATTTGAGGACCGGNTG
GTGAGCACCCTACCTGATGCTCCATGGGGGAACTACAGCTTCATCGACTCCATTGGTAGA
AGCAAAAACTNCCTGGACTCCCTTTTTGAN
Restriction Sites NotI-NotI     
ACCN NM_016166
ORF Size 1956 bp
Insert Size 2320
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_016166.1, NP_057250.1
RefSeq Size 2309
RefSeq ORF 1956
Locus ID 8554
Domains SAP, zf-MIZ
Protein Families Druggable Genome, Transcription Factors
Protein Pathways Jak-STAT signaling pathway, Pathways in cancer, Small cell lung cancer, Ubiquitin mediated proteolysis
Gene Summary This gene encodes a member of the protein inhibitor of activated STAT (PIAS) family. PIAS proteins function as SUMO E3 ligases and play important roles in many cellular processes by mediating the sumoylation of target proteins. This protein plays a central role as a transcriptional coregulator of numerous cellular pathways includign the STAT1 and nuclear factor kappaB pathways. Alternate splicing results in multiple transcript variants. [provided by RefSeq, Mar 2016]
Transcript Variant: This variant (2) uses an alternate 5' structure which results in a distinct 5' UTR and 5' coding region compared to variant 1. The encoded isoform (2) is shorter and has a distinct N-terminus compared to isoform 1. Sequence Note: This RefSeq record was created from transcript and genomic sequence data to make the sequence consistent with the reference genome assembly. The genomic coordinates used for the transcript record were based on transcript alignments.

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