BAP1 (NM_004656) Human Untagged Clone

SKU
SC117256
BAP1 (untagged)-Human BRCA1 associated protein-1 (ubiquitin carboxy-terminal hydrolase) (BAP1)
  $1,002.00
In Stock*
Specifications
Specifications
Product Data
Type Human Untagged Clone
Target Symbol BAP1
Synonyms hucep-6; HUCEP-13; UCHL2
Vector pCMV6-AC
E. coli Selection Ampicillin (100 ug/mL)
Mammalian Cell Selection Neomycin
Sequence Data
Fully Sequenced ORF
>OriGene sequence for NM_004656.2 GCCCGTTGTCTGTGTGTGGGACTGAGGGGCCCCGGGGGCGGTGGGGGCTCCCGGTGGGGG
CAGCGGTGGGGAGGGAGGGCCTGGACATGGCGCTGAGGGGCCGCCCCGCGGGAAGATGAA
TAAGGGCTGGCTGGAGCTGGAGAGCGACCCAGGCCTCTTCACCCTGCTCGTGGAAGATTT
CGGTGTCAAGGGGGTGCAAGTGGAGGAGATCTACGACCTTCAGAGCAAATGTCAGGGCCC
TGTATATGGATTTATCTTCCTGTTCAAATGGATCGAAGAGCGCCGGTCCCGGCGAAAGGT
CTCTACCTTGGTGGATGATACGTCCGTGATTGATGATGATATTGTGAATAACATGTTCTT
TGCCCACCAGCTGATACCCAACTCTTGTGCAACTCATGCCTTGCTGAGCGTGCTCCTGAA
CTGCAGCAGCGTGGACCTGGGACCCACCCTGAGTCGCATGAAGGACTTCACCAAGGGTTT
TAGCCCTGAGAGCAAAGGATATGCGATTGGCAATGCCCCGGAGTTGGCCAAGGCCCATAA
TAGCCATGCCAGGCCCGAGCCACGCCACCTCCCTGAGAAGCAGAATGGCCTTAGTGCAGT
GCGGACCATGGAGGCGTTCCACTTTGTCAGCTATGTGCCTATCACAGGCCGGCTCTTTGA
GCTGGATGGGCTGAAGGTCTACCCCATTGACCATGGGCCCTGGGGGGAGGACGAGGAGTG
GACAGACAAGGCCCGGCGGGTCATCATGGAGCGTATCGGCCTCGCCACTGCAGGGGAGCC
CTACCACGACATCCGCTTCAACCTGATGGCAGTGGTGCCCGACCGCAGGATCAAGTATGA
GGCCAGGCTGCATGTGCTGAAGGTGAACCGTCAGACAGTACTAGAGGCTCTGCAGCAGCT
GATAAGAGTAACACAGCCAGAGCTGATTCAGACCCACAAGTCTCAAGAGTCACAGCTGCC
TGAGGAGTCCAAGTCAGCCAGCAACAAGTCCCCGCTGGTGCTGGAAGCAAACAGGGCCCC
TGCAGCCTCTGAGGGCAACCACACAGATGGTGCAGAGGAGGCGGCTGGTTCATGCGCACA
AGCCCCATCCCACAGCCCTCCCAACAAACCCAAGCTAGTGGTGAAGCCTCCAGGCAGCAG
CCTCAATGGGGTTCACCCCAACCCCACTCCCATTGTCCAGCGGCTGCCGGCCTTTCTAGA
CAATCACAATTATGCCAAGTCCCCCATGCAGGAGGAAGAAGACCTGGCGGCAGGTGTGGG
CCGCAGCCGAGTTCCAGTCCGCCCACCCCAGCAGTACTCAGATGATGAGGATGACTATGA
GGATGACGAGGAGGATGACGTGCAGAACACCAACTCTGCCCTTAGGTATAAGGGGAAGGG
AACAGGGAAGCCAGGGGCATTGAGCGGTTCTGCTGATGGGCAACTGTCAGTGCTGCAGCC
CAACACCATCAACGTCTTGGCTGAGAAGCTCAAAGAGTCCCAGAAGGACCTCTCAATTCC
TCTGTCCATCAAGACTAGCAGCGGGGCTGGGAGTCCGGCTGTGGCAGTGCCCACACACTC
GCAGCCCTCACCCACCCCCAGCAATGAGAGTACAGACACGGCCTCTGAGATCGGCAGTGC
TTTCAACTCGCCACTGCGCTCGCCTATCCGCTCAGCCAACCCGACGCGGCCCTCCAGCCC
TGTCACCTCCCACATCTCCAAGGTGCTTTTTGGAGAGGATGACAGCCTGCTGCGTGTTGA
CTGCATACGCTACAACCGTGCTGTCCGTGATCTGGGTCCTGTCATCAGCACAGGCCTGCT
GCACCTGGCTGAGGATGGGGTGCTGAGTCCCCTGGCGCTGACAGAGGGTGGGAAGGGTTC
CTCGCCCTCCATCAGACCAATCCAAGGCAGCCAGGGGTCCAGCAGCCCAGTGGAGAAGGA
GGTCGTGGAAGCCACGGACAGCAGAGAGAAGACGGGGATGGTGAGGCCTGGCGAGCCCTT
GAGTGGGGAGAAATACTCACCCAAGGAGCTGCTGGCACTGCTGAAGTGTGTGGAGGCTGA
GATTGCAAACTATGAGGCGTGCCTCAAGGAGGAGGTAGAGAAGAGGAAGAAGTTCAAGAT
TGATGACCAGAGAAGGACCCACAACTACGATGAGTTCATCTGCACCTTTATCTCCATGCT
GGCTCAGGAAGGCATGCTGGCCAACCTAGTGGAGCAGAACATCTCCGTGCGGCGGCGCCA
AGGGGTCAGCATCGGCCGGCTCCACAAGCAGCGGAAGCCTGACCGGCGGAAACGCTCTCG
CCCCTACAAGGCCAAGCGCCAGTGAGGACTGCTGGCCCTGACTCTGCAGCCCACTCTTGC
CGTGTGGCCCTCACCAGGGTCCTTCCCTGCCCCACTTCCCCTTTTCCCAGTATTACTGAA
TAGTCCCAGCTGGAGAGTCCAGGCCCTGGGAATGGGAGGAACCAGGCCACATTCCTTCCA
TCGTGCCCTGAGGCCTGACACGGCAGATCAGCCCCATAGTGCTCAGGAGGCAGCATCTGG
AGTTGGGGCACAGCGAGGTACTGCAGCTTCCTCCACAGCCGGCTGTGGAGCAGCAGGACC
TGGCCCTTCTGCCTGGGCAGCAGAATATATATTTTACCTATCAAAAAAAAAAAAAAAAAA
Restriction Sites NotI-NotI |
ACCN NM_004656
Insert Size 3520 bp
OTI Disclaimer Due to the inherent nature of this plasmid, standard methods to replicate additional amounts of DNA in E. coli are highly likely to result in mutations and/or rearrangements. Therefore, OriGene does not guarantee the capability to replicate this plasmid DNA. Additional amounts of DNA can be purchased from OriGene with batch-specific, full-sequence verification at a reduced cost. Please contact our customer care team at custsupport@origene.com or by calling 301.340.3188 option 3 for pricing and delivery.

The molecular sequence of this clone aligns with the gene accession number as a point of reference only. However, individual transcript sequences of the same gene can differ through naturally occurring variations (e.g. polymorphisms), each with its own valid existence. This clone is substantially in agreement with the reference, but a complete review of all prevailing variants is recommended prior to use. More info
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 Method 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.
Note Plasmids are not sterile.  For experiments where strict sterility is required, filtration with 0.22um filter is required.
Shipping Ambient
Reference Data
RefSeq NM_004656.2, NP_004647.1
RefSeq Size 3599 bp
RefSeq ORF 2190 bp
Locus ID 8314
UniProt ID Q92560
Cytogenetics 3p21.1
Domains Peptidase_C12
Protein Families Druggable Genome, Protease
Summary This gene belongs to the ubiquitin C-terminal hydrolase subfamily of deubiquitinating enzymes that are involved in the removal of ubiquitin from proteins. The encoded enzyme binds to the breast cancer type 1 susceptibility protein (BRCA1) via the RING finger domain of the latter and acts as a tumor suppressor. In addition, the enzyme may be involved in regulation of transcription, regulation of cell cycle and growth, response to DNA damage and chromatin dynamics. Germline mutations in this gene may be associated with tumor predisposition syndrome (TPDS), which involves increased risk of cancers including malignant mesothelioma, uveal melanoma and cutaneous melanoma. provided by RefSeq, May 2013
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Documents
Resources
"NM_004656" in other vectors (7)
SKU Description Size Price
RC200378 BAP1 (Myc-DDK-tagged)-Human BRCA1 associated protein-1 (ubiquitin carboxy-terminal hydrolase) (BAP1) 10 ug
$1,001.00
RC200378L1 Lenti ORF clone of Human BRCA1 associated protein-1 (ubiquitin carboxy-terminal hydrolase) (BAP1), Myc-DDK-tagged 10 ug
$1,301.00
RC200378L2 Lenti ORF clone of Human BRCA1 associated protein-1 (ubiquitin carboxy-terminal hydrolase) (BAP1), mGFP tagged 10 ug
$1,301.00
RC200378L3 Lenti ORF clone of Human BRCA1 associated protein-1 (ubiquitin carboxy-terminal hydrolase) (BAP1), Myc-DDK-tagged 10 ug
$1,301.00
RC200378L4 Lenti ORF clone of Human BRCA1 associated protein-1 (ubiquitin carboxy-terminal hydrolase) (BAP1), mGFP tagged 10 ug
$1,301.00
RG200378 BAP1 (tGFP-tagged) - Human BRCA1 associated protein-1 (ubiquitin carboxy-terminal hydrolase) (BAP1) 10 ug
$1,201.00
SC320669 BAP1 (untagged)-Human BRCA1 associated protein-1 (ubiquitin carboxy-terminal hydrolase) (BAP1) 10 ug
$1,002.00

file-alt Citations

BAP1 and YY1 regulate expression of death receptors in malignant pleural mesothelioma
Ishii, Kolluri, Pennycuick et al
J Biol Chem (2021) 297 (5), 101223 DOI: 10.1016/j.jbc.2021.101223
Cited by 12
AI Summary: OriGene's pCMV6-AC BAP1 plasmid (SC117256) was used as the source for full-length BAP1 cDNA, enabling the authors to study the effects of BAP1 overexpression and mutation on death receptor regulation in malignant pleural mesothelioma.
Snippet: oblotting was performed as described previously with anti-BAP1 antibody (sc-28383;Santa Cruz). Plasmids Full-length BAP1 complementary DNA was amplified by PCR from pCMV6-AC BAP1 plasmid (SC117256;Origene) and cloned into the lentiviral plasmid pCCL-CMV-flT vector. Vectors expressing BAP1-mutant constructs were generated by site-directed mutagenesis (E0554;New England Biolabs) of the pCCL-CMV
Loss of functional BAP1 augments sensitivity to TRAIL in cancer cells
Kolluri, Alifrangis, Kumar et al
Elife (2018) 7 DOI: 10.7554/eLife.30224
AI Summary: OriGene’s pCMV6-AC BAP1 plasmid (SC117256) was used as the source of full-length BAP1 cDNA for generating expression constructs to study the role of BAP1 in cancer cell sensitivity to TRAIL.
Snippet: …BAP1 has emerged as a key driver of tumorigenesis in MM (Bueno et al., 2016). … While next-generation sequencing reve;Full-length BAP1 cDNA was amplified by PCR from pCMV6-AC BAP1 plasmid (Origene (Rockville, MD;SC117256) and cloned into the lentiviral plasmid pCCL-CMV-flT vector previously described (Yuan et al., 2015) in place of flT via BamHI and SalI sites, creating the BAP1 vector designated pCCL-CMV-BAP1. Vectors expressing mutant BAP1 constructs were generated by site-directed mutagenesis (New England Biolabs) of the pCCL-CMV-BAP1 vector. …
FigureFigureFigure
BAP1 dependent expression of long non-coding RNA NEAT-1 contributes to sensitivity to gemcitabine in cholangiocarcinoma
Parasramka, Yan, Wang et al
Mol. Cancer (2017) 16 (1), 22 DOI: 10.1186/s12943-017-0587-x
AI Summary: OriGene’s pCMV6-AC-BAP1 human cDNA clone plasmid was used to manipulate BAP1 expression in cholangiocarcinoma cells, enabling the study of its role in drug sensitivity and tumor behavior.
Snippet: After 6 h, the medium was replaced with the respective complete culture medium containing 10% serum and the cells were incubated for 48 h before further study. BAP1 human cDNA clone, pCMV6-AC-BAP1 plasmid was purchased from Origene Technologies, Rockville ... Cite SaveSaving
FigureFigureFigure
Cancer-associated ASXL1 mutations may act as gain-of-function mutations of the ASXL1-BAP1 complex
Balasubramani, Larjo, Bassein et al
Nat Commun (2015) 6, 7307 DOI: 10.1038/ncomms8307
Cited by 198
AI Summary: OriGene contributed pCMV-driven plasmids encoding full-length human BAP1 and ASXL1, which were used to study the effects of ASXL1 truncations on the activity of the ASXL1-BAP1 complex in this research.
Snippet: Mammalian cytomegalovirus (CMV) promoter (pCMV)-driven plasmids that encode full-length human BAP1 and ASXL1 were purchased from Origene (Rockville, MD)
Mechanisms of TRAIL resistance
Kumar
Thesis (2018)
Snippet: The BAP1 vector pCCL-CMV-BAP1 had previously been generated by K Kolluri by PCR amplification of BAP1 coding cDNA using a pCMV6-AC BAP1 plasmid (Origene-SC117256) as a template and subsequent insertion of the BAP1 cDNA into a lentiviral vector previously used in the laboratory, pCCLCMV-flT, in place of flT via BamHI and SalI restriction sites (Figure 2-1) [140]
Showing 1-5 of 5 papers.
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