PIAS2 (NM_004671) Human Untagged Clone

CAT#: SC125358

PIAS2 (untagged)-Human protein inhibitor of activated STAT, 2 (PIAS2), transcript variant beta


  "NM_004671" in other vectors (6)

Reconstitution Protocol

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    • 10 ug

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Specifications

Product Data
Type Human Untagged Clone
Tag Tag Free
Symbol PIAS2
Synonyms ARIP3; DIP; MIZ1; PIASX; SIZ2; ZMIZ4
Vector pCMV6-XL5
E. coli Selection Ampicillin (100 ug/mL)
Mammalian Cell Selection None
Sequence Data
>OriGene ORF within SC125358 sequence for NM_004671 edited (data generated by NextGen Sequencing)
ATGGCGGATTTCGAAGAGTTGAGGAATATGGTTTCTAGTTTTAGGGTTTCTGAACTACAA
GTATTACTAGGCTTTGCTGGACGGAATAAAAGTGGACGCAAGCATGACCTCCTGATGAGG
GCGCTGCATTTATTGAAGAGCGGCTGCAGCCCTGCGGTTCAGATTAAAATCCGAGAATTG
TATAGACGCCGATATCCACGAACTCTTGAAGGACTTTCTGATTTATCCACAATCAAATCA
TCGGTTTTCAGTTTGGATGGTGGCTCATCACCTGTAGAACCTGACTTGGCCGTGGCTGGA
ATCCACTCGTTGCCTTCCACTTCAGTTACACCTCACTCACCATCCTCTCCTGTTGGTTCT
GTGCTGCTTCAAGATACTAAGCCCACATTTGAGATGCAGCAGCCATCTCCCCCAATTCCT
CCTGTCCATCCTGATGTGCAGTTAAAAAATCTGCCCTTTTATGATGTCCTTGATGTTCTC
ATCAAGCCCACGAGTTTAGTTCAAAGCAGTATTCAGCGATTTCAAGAGAAGTTTTTTATT
TTTGCTTTGACACCTCAACAAGTTAGAGAGATATGCATATCCAGGGATTTTTTGCCAGGT
GGTAGGAGAGATTATACAGTCCAAGTTCAGTTGAGACTTTGCCTGGCAGAGACAAGTTGC
CCTCAAGAAGATAACTATCCAAATAGTCTATGTATAAAAGTAAATGGGAAGCTATTTCCT
TTGCCTGGCTATGCACCACCGCCTAAAAATGGGATTGAACAGAAGCGCCCTGGACGCCCC
TTGAATATTACATCTTTAGTTAGGTTATCTTCAGCTGTGCCAAACCAAATTTCCATTTCT
TGGGCATCAGAAATTGGGAAGAATTACTCTATGTCTGTATATCTTGTACGGCAGCTTACA
TCAGCCATGTTATTACAGAGATTAAAAATGAAAGGTATTAGAAACCCTGATCATTCCAGA
GCACTAATTAAAGAAAAACTTACTGCAGATCCTGATAGTGAAATTGCTACAACTAGCCTT
CGGGTATCCTTGATGTGCCCTTTAGGAAAAATGAGGCTGACAATCCCATGCCGTGCAGTG
ACTTGTACACATCTGCAGTGTTTTGATGCTGCCCTCTATCTACAAATGAATGAGAAAAAG
CCCACCTGGATTTGTCCTGTGTGTGACAAAAAAGCTGCCTATGAAAGTCTAATATTAGAT
GGGCTTTTTATGGAAATTCTCAATGACTGTTCTGATGTAGATGAGATCAAATTCCAAGAA
GATGGTTCTTGGTGTCCAATGAGACCGAAGAAAGAAGCTATGAAAGTATCCAGCCAACCG
TGTACAAAAATAGAAAGTTCAAGCGTCCTCAGTAAGCCTTGTTCAGTGACTGTAGCCAGT
GAGGCAAGCAAGAAGAAAGTAGATGTTATTGATCTTACAATAGAAAGCTCTTCTGACGAA
GAGGAAGACCCTCCTGCCAAAAGGAAATGCATCTTTATGTCAGAAACACAAAGCAGCCCA
ACCAAAGGGGTTCTCATGTATCAGCCATCTTCTGTAAGGGTGCCCAGTGTGACTTCGGTT
GATCCTGCTGCTATTCCGCCTTCATTAACAGACTACTCAGTACCATTCCACCATACGCCA
ATATCAAGCATGTCATCAGATTTGCCAGGTTTGGATTTTCTTTCCCTTATTCCAGTTGAT
CCCCAGTACTGTCCTCCTATGTTTTTGGATAGTCTCACCTCACCCTTAACAGCAAGCAGT
ACGTCTGTCACCACCACCAGCTCCCATGAAAGCAGTACTCATGTTAGTTCATCCAGCAGC
AGGAGTGAGACAGGGGTCATAACCAGCAGTGGAAGTAACATTCCTGACATCATCTCATTG
GACTAA

Clone variation with respect to NM_004671.3
>OriGene 5' read for NM_004671 unedited
TTGTAATACGACTCACTATAGGGCGGCCGCGAATTCGGCACGAGGGCGGCGGCGGCCGCG
GCGTCTTAAGCGGCGCCCAGTGCAGGATGGTGCTGGAGGCGGCGGCGGCCGTGGTGGCGG
CAGCGTCGTTGGCGGCAGCGGGAGTGGGTGCGGCGGCAGCGGCGGCGGCGCCCGCGGGTG
GTATAAAATGGCGGATTTCGAAGAGTTGAGGAATATGGTTTCTAGTTTTAGGGTTTCTGA
ACTACAAGTATTACTAGGCTTTGCTGGACGGAATAAAAGTGGACGCAAGCATGACCTCCT
GATGAGGGCGCTGCATTTATTGAAGAGCGGCTGCAGCCCTGCGGTTCAGATTAAAATCCG
AGAATTGTATAGACGCCGATATCCACGAACTCTTGAAGGACTTTCTGATTTATCCACAAT
CAAATCATCGGTTTTCAGTTTGGATGGTGGCTCATCACCTGTAGAACCTGACTTGGCCGT
GGCTGGAATCCACTCGTTGCCTTCCACTTCAGTTACACCTCACTCACCATCCTCTNCTGT
TGGTTCTGTGCTGCTTCAAGATACTAAGCCCACATTTGAGATGCAGCAGCCATCTCCCCC
AATTCCTCCTGTCCATCCTGATGTGCAGTTAAAAAATCTGCCCTTTTATGATGTCCTTGA
TGTTCTCATCAAGCCCACGAGTTTAGTTCANAGCAGTATTCAGCGATTTAAAGAGAAGTT
NTTTATTNTTGCTTTGACACCTCAAACAGTTAGAGAGATATGCATATCCAGNNGATTTTT
TGCCANNGTGGTANNGAGAGATTATACAGTCCAAGTTCAGTTGAGACTTTGCCTGGCAGA
GACAAGTTGCCCTCAAGAAGATNACTATCCCAATAGTCTATGTATAAAAAAGTAATGGAA
GCTATTTCCTTTGCCTGGCTATGACCCACCGCCTAAANATGG
>OriGene 3' read for NM_004671 unedited
NAAAGACATTCTCATCTTGTACTTCANNTGCTCTTTATTTAACAAAACTTTTTTCACTGA
TTTGTAGACTCCATCCATTAACGTATGAAAGTGAAATCCATCTCTCAGGAAGATACAGTT
ATGGTTGAATGTATCTGATGCTGAGAGTACAGCATAATTAAAAAAAATCCTTGCCTGTCA
TTTTGGTTTCTTGTTGCGAGTCTTTTGGGGTTTCCCCCTCTCAAAAAGCCAAAAAACCCC
TTTTGGGTTTCTTTGAAATTCCCCCCCTTTTTTTAAAACAAAAAAAAAAAAAACCTTTTC
CCCCCAGTTATTCTCCTCCCACAAAAGTCTCCTTCTTGGATAATAATTCCCCCACCACAC
GGGGGGGCCCCCTTTCTCTCTCAAAAAAATTTTATTCGACTGGGAGAATTTTCCCCCTCT
TTCTTTTTTTCCTACCCCTCTTCTTTTCCCCTCCCGTGTTTTTCGTTAGACAACATCCTC
CCCCTCTTCTCTCACTTCACTCCCGCATGCTCGGCCCCGCTTATCACCGTCTTCCTTTTC
ATTTCCGGCGGAATCGGCCCCCTTCCCCCCCCACCCGTTTTATCCCCGTCCCCCTAGTTT
CCCCCTCTCTGTATCATGTCGGCCTCTTCTTCCCCTTCCCCCTACATTCCTATTCCCCCC
GCTGTTCTTCCCTATATTTCACCTCCTTTTCCGTTTCCTCATCCTTTTTTCATCTTCTCT
CCATTTCGCCTTTTGTTCTCGCCCTCGTCTCACTGTTTTCCGTCCCTTCTCTCCTTTTTC
TACACGTGCCTACTTCCTCGTTGTCCCCACTCTCGCCCCCCTTTCTTTTCCCCTTCTTGT
TCGTTCGGTGCCCCGCTTTTTTTTCTCCCCATGCTCCCTTTTGGG
Restriction Sites NotI-NotI     
ACCN NM_004671
ORF Size 1866 bp
Insert Size 2500
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_004671.2, NP_004662.2
RefSeq Size 2360
RefSeq ORF 1866
Locus ID 9063
Domains SAP, zf-MIZ
Protein Families Stem cell - Pluripotency, Stem cell relevant signaling - JAK/STAT signaling pathway, 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 family, which function as SUMO E3 ligases and play important roles in many cellular processes by mediating the sumoylation of target proteins. Alternatively spliced transcript variants encoding multiple isoforms have been observed for this gene. Isoforms of the encoded protein enhance the sumoylation of specific target proteins including the p53 tumor suppressor protein, c-Jun, and the androgen receptor. A pseudogene of this gene is located on the short arm of chromosome 4. The symbol MIZ1 has also been associated with ZBTB17 which is a different gene located on chromosome 1. [provided by RefSeq, Aug 2017]
Transcript Variant: This variant (beta) encodes isoform (beta). 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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