BCL2 (NM_000633) Human Untagged Clone

SKU
SC125546
BCL2 (untagged)-Human B-cell CLL/lymphoma 2 (BCL2), nuclear gene encoding mitochondrial protein, transcript variant alpha
  $450.00
In Stock*
Specifications
Specifications
Product Data
Type Human Untagged Clone
Target Symbol BCL2
Synonyms Bcl-2; PPP1R50
Vector pCMV6-XL4
E. coli Selection Ampicillin (100 ug/mL)
Mammalian Cell Selection None
Sequence Data
Fully Sequenced ORF
>NCBI ORF sequence for NM_000633, the custom clone sequence may differ by one or more nucleotides


GAATTCCCGGGATATCGTCGACCCACGCGTCCGCTGGAGAGTGCTGAAGATTGATGGGATCGTTGCCTTA
TGCATTTGTTTTGGTTTTACAAAAAGGAAACTTGACAGAGGATCATGCTGTACTTAAAAAATACAACATC
ACAGAGGAAGTAGACTGATATTAACAATACTTACTAATAATAACGTGCCTCATGAAATAAAGATCCGAAA
GGAATTGGAATAAAAATTTCCTGCATCTCATGCCAAGGGGGAAACACCAGAATCAAGTGTTCCGCGTGAT
TGAAGACACCCCCTCGTCCAAGAATGCAAAGCACATCCAATAAAATAGCTGGATTATAACTCCTCTTCTT
TCTCTGGGGGCCGTGGGGTGGGAGCTGGGGCGAGAGGTGCCGTTGGCCCCCGTTGCTTTTCCTCTGGGAA
GGATGGCGCACGCTGGGAGAACGGGGTACGATAACCGGGAGATAGTGATGAAGTACATCCATTATAAGCT
GTCGCAGAGGGGCTACGAGTGGGATGCGGGAGATGTGGGCGCCGCGCCCCCGGGGGCCGCCCCCGCACCG
GGCATCTTCTCCTCCCAGCCCGGGCACACGCCCCATCCAGCCGCATCCCGGGACCCGGTCGCCAGGACCT
CGCCGCTGCAGACCCCGGCTGCCCCCGGCGCCGCCGCGGGGCCTGCGCTCAGCCCGGTGCCACCTGTGGT
CCACCTGACCCTCCGCCAGGCCGGCGACGACTTCTCCCGCCGCTACCGCCGCGACTTCGCCGAGATGTCC
AGCCAGCTGCACCTGACGCCCTTCACCGCGCGGGGACGCTTTGCCACGGTGGTGGAGGAGCTCTTCAGGG
ACGGGGTGAACTGGGGGAGGATTGTGGCCTTCTTTGAGTTCGGTGGGGTCATGTGTGTGGAGAGCGTCAA
CCGGGAGATGTCGCCCCTGGTGGACAACATCGCCCTGTGGATGACTGAGTACCTGAACCGGCACCTGCAC
ACCTGGATCCAGGATAACGGAGGCTGGGATGCCTTTGTGGAACTGTACGGCCCCAGCATGCGGCCTCTGT
TTGATTTCTCCTGGCTGTCTCTGAAGACTCTGCTCAGTTTGGCCCTGGTGGGAGCTTGCATCACCCTGGG
TGCCTATCTGGGCCACAAGTGAAGTCAACATGCCTGCCCCAAACAAATATGCAAAAGGTTCACTAAAGCA
GTAGAAATAATATGCATTGTCAGTGATGTACCATGAAACAAAGCTGCAGGCTGTTTAAGAAAAAATAACA
CACATATAAACATCACACACACAGACAGACACACACACACACAACAATTAACAGTCTTCAGGCAAAACGT
CGAATCAGCTATTTACTGCCAAAGGGAAA


5' Read Nucleotide Sequence
>OriGene 5' read for NM_000633 unedited
NGTTCACGTTAAAATTTGTAATAGACTCACTATAGGCGGCCGCGNAATCAGATCTGGTAC
CGGTCCGGAATTCCCGGGATATCGTCGACCCACGCGTCCGCTGGAGAGTGCTGAAGATTG
ATGGGATCGTTGCCTTATGCATTTGTTTTGGTTTTACAAAAAGGAAACTTGACAGAGGAT
TCATGCTGTACTTAAAAAATACAACATCACAGAGGAAGTAGACTGATATTAACAATACTT
ACTAATAATAACGTGCCTCATGAAATAAAGATCCGAAAGGAATTGGAATAAAAATTTCCT
GCATCTCATGCCAAGGGGGAAACACCAGAATCAAGTGTTCCGCGTGATTGAAGACACCCC
CTCGTCCAAGAATGCAAAGCACATCCAATAAAATAGCTGGATTATAACTCCTCTTCTTTC
TCTGGGGGCCGTGGGGTGGGAGCTGGGGCGAGAGGTGCCGTTGGCCCCCGTTGCTTTTCC
TCTGGGAAGGATGGCGCACGCTGGGAGAACGGGGTACGATAACCGGGAGATAGTGATGAA
GTACATCCATTATAAGCTGTCGCAGAGGGGCTACGAGTGGGATGCCGGAGAATGTTGGCG
CCGCGCCCCCGGGGGCCGCCCCCGCACCGGGCATCTTCTCCTCCCAGCCCGGGCACACGC
CCCATCCAGCCGCATCCCGGGACCCGGTCGCCAGGACCTCGCCGCTGCAGACCCCCGCTG
CCCNCGGCGCGGCCGCGGGGGCCTGCGCTCAGCCCGGTGCCACCCTGTGTCCACCTGACC
CTCGCCAGCCNGCGACGACTTCTCCGCCGCTACCGCCGCGACTTCGCCGAGATGTTCAGC
CAGCTGCACCTGACGCCTTTACCGCGCCGGGGACGCTTTGCACCGTGGGGTGGAAGAGCT
CTTCAGGNACGGGGTG
3' Read Nucleotide Sequence
>OriGene 3' read for NM_000633 unedited
CTGGGCCATTGGNGATGGCAACTTCCAGGNCCAGNAAAGCACTGGGGNAGGGTCACAGGN
ATGCCACCCGGGATCTGTTCAGGAAACAGCTATGACCGCGGCCGCCCTTTTTTTTTTTTT
TTAATGCCCCAGGATGTACAGATAACCCCCATATTCCACACCTGGAACTTTTTTTTTGTC
AGGTTTTCAAATAAAACCAAACTACAGTGACAAGATAATGTTTTACATGTAATTCCATAG
ACAGGGGTCAATTAATCCATGACACCTCACTTCAATGCTTCTTTTAGGATTTGTGACCCT
CTCCAAAGTCATTTAAAGCCTTGCTTTAAACTCACAGGTGGGCCAAGGCCACACAGCCAA
CGTGCCATGTGCTACAGCCAAAATGGGCCGTGGCCATTGCCTCTCCTCACGTTCCCAGCC
TTCACCATGTCCTTCTGATAGGAAGGGCCCAGGGCCTCTGTTCCTTCCCTCTACAGTGAT
ACATGTCTTAAGAAGGGTCGTGGCTCCCATGCTCCACGTGAAAACGGGCCTACCTGGAGG
GCCCCAGGGTGACAGGCCCAGCCACACCCCTCTACTGCTCTTTCTTGACAGTGGAATTCT
GAGCTCCATCAGCTTCCAGACATTCGGAGACCACACTGCCCTGTTGATCATCCCTGGAGG
AGGCCAGTGAGGGCCCCGGCTCAGTTCCAGGACCAGGCCTCCAAGCTGGGACACAGGCAG
GTTCTGCGGACTTCGGTCTCCTAAAACAGGCACTTGTGGCGGCCTGATGCTCTGGGTAAC
TCTAGCCTTCCTGATGCGGAAGTCACCGAAATGTTCACTTCCTCAAGTTCCAGAGGATTC
TGTTTCTTACTCAGACAGAGCCAGTATTGGGAGTTGGGGGGGGTGCGTATCCAAAATATA
TGAATATACACAATCG
Restriction Sites Please inquire |
ACCN NM_000633
Insert Size 3050 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_000633.2, NP_000624.2
RefSeq Size 6492 bp
RefSeq ORF 720 bp
Locus ID 596
UniProt ID P10415
Cytogenetics 18q21.33
Protein Families Druggable Genome, ES Cell Differentiation/IPS, Stem cell - Pluripotency, Transmembrane
Protein Pathways Amyotrophic lateral sclerosis (ALS), Apoptosis, Colorectal cancer, Focal adhesion, Neurotrophin signaling pathway, Pathways in cancer, Prostate cancer, Small cell lung cancer
Summary This gene encodes an integral outer mitochondrial membrane protein that blocks the apoptotic death of some cells such as lymphocytes. Constitutive expression of BCL2, such as in the case of translocation of BCL2 to Ig heavy chain locus, is thought to be the cause of follicular lymphoma. Alternative splicing results in multiple transcript variants. provided by RefSeq, Feb 2016
Transcript Variant: This variant (alpha) represents the longer transcript and encodes the longer isoform (alpha).
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Documents
Resources
"NM_000633" in other vectors (6)
SKU Description Size Price
RC204498 BCL2 (Myc-DDK-tagged)-Human B-cell CLL/lymphoma 2 (BCL2), nuclear gene encoding mitochondrial protein, transcript variant alpha 10 ug
$450.00
RC204498L1 Lenti ORF clone of Human B-cell CLL/lymphoma 2 (BCL2), nuclear gene encoding mitochondrial protein, transcript variant alpha, Myc-DDK-tagged 10 ug
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RC204498L2 Lenti ORF clone of Human B-cell CLL/lymphoma 2 (BCL2), nuclear gene encoding mitochondrial protein, transcript variant alpha, mGFP tagged 10 ug
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RC204498L3 Lenti ORF clone of Human B-cell CLL/lymphoma 2 (BCL2), nuclear gene encoding mitochondrial protein, transcript variant alpha, Myc-DDK-tagged 10 ug
$750.00
RC204498L4 Lenti ORF clone of Human B-cell CLL/lymphoma 2 (BCL2), nuclear gene encoding mitochondrial protein, transcript variant alpha, mGFP tagged 10 ug
$750.00
RG204498 BCL2 (tGFP-tagged) - Human B-cell CLL/lymphoma 2 (BCL2), nuclear gene encoding mitochondrial protein, transcript variant alpha 10 ug
$650.00

file-alt Citations

Bcl-2 inhibitors enhance FGFR inhibitor-induced mitochondrial-dependent cell death in FGFR2 mutant endometrial cancer
Packer, Stehbens, Bonazzi et al
Mol Oncol (2018)
AI Summary: OriGene's Bcl-2 (SC125546) and Bcl-XL (SC127825) overexpression plasmids were used to demonstrate that mitochondrial-dependent cell death induced by FGFR inhibitors in FGFR2-mutant endometrial cancer cells can be blocked by overexpressing these anti-apoptotic proteins.
Snippet: selection took place 48 h post infection. Overexpression Plasmids Bcl-2 and Bcl-XL constructs were obtained from Origene (SC125546 and SC127825) and subsequently subcloned into pEF1αIRES.neo.3. AN3CA and JHUEM2 cells were transfected with
Prolonged engraftment of transplanted hepatocytes in the liver by transient pro-survival factor supplementation using ex vivo mRNA transfection
Matsui, Uchida, Hayashi et al
J Control Release (2018) 285, 1-11 DOI: 10.1016/j.jconrel.2018.06.033
AI Summary: OriGene’s pCMV-XL4-Bcl2 vector was used as the source of the Bcl-2 gene for mRNA synthesis, enabling transient pro-survival factor expression to enhance hepatocyte engraftment in the study.
Snippet: Briefly, a template pDNA was prepared by cloning the Bcl-2 expressing portion of the pCMV-XL4-Bcl2 vector (OriGene, Rockville, MD, USA), and a sequence comprised of 120 A/T nucleotides, into pSP73 (Promega, Madison, WI, USA) downstream of a T7 promoter
Inhibition of Bcl-2 potentiates AZD-2014-induced anti-head and neck squamous cell carcinoma cell activity
Li, Cui
Biochem. Biophys. Res. Commun. (2016)
Cited by 12
AI Summary: OriGene contributed Bcl-2 shRNA lentiviruses (Bcl-2-shRNA-a and Bcl-2-shRNA-b) used to knock down Bcl-2 expression in SQ20B cells, enabling the study of Bcl-2’s role in resistance to AZD-2014 in head and neck squamous cell carcinoma.
Snippet: Each non-overlapping Bcl-2-shRNA (“-a/-b”, both were designed by ORIGENE, Shanghai, China) lentivirus (10 μl/ml) was added to SQ20B cells for 24 h. Afterwards, cells were cultured in fresh medium, and were subjected to puromycin (2.5 μg/ml, Sigma) selection ... Cite SaveSaving
Apoptosis as the focus of an authentic research experience in a cell physiology laboratory
Byrd
Adv Physiol Educ (2016) 40 (2), 257-64 DOI: 10.1152/advan.00176.2015
Cited by 4
AI Summary: In this study, the OriGene Bcl-2-containing plasmid (SC125546) was considered as a potential tool for student experiments to rescue cells from apoptosis, but ultimately was not used due to cost and time limitations.
Snippet: Cell transfection with a Bcl-2-containing plasmid (SC125546, Origene) and small interfering RNA knockdown of intrinsic cascade elements were discussed as possible “rescue” techniques but were rejected because of price and time constraints for experiments. ... Cite SaveSaving
Messenger RNA-based therapeutics for the treatment of apoptosis-associated diseases
Matsui, Uchida, Ishii et al
Sci Rep (2015) 5, 15810 DOI: 10.1038/srep15810
Cited by 94
AI Summary: OriGene’s pCMV-XL4-Bcl2 vector was used as the plasmid DNA template for in vitro transcription of Bcl-2 mRNA, enabling the study of mRNA-based anti-apoptotic therapy in the mouse model.
Snippet: pDNA templates for IVT were constructed from the pAcGFP vector (Clontech, Mountain View, CA, USA) for GFP, the pORF-mEPOv18 vector (Invitrogen, Carlsbad, CA, USA) for erythropoietin, and the pCMV-XL4-Bcl2 vector (OriGene, Rockville, MD, USA) for Bcl-2. The ... Cite SaveSaving
FigureFigureFigure
uPAR and cathepsin B downregulation induces apoptosis by targeting calcineurin A to BAD via Bcl-2 in glioma
Malla, Gopinath, Gondi et al
J. Neurooncol. (2012) 107 (1), 69-80 DOI: 10.1007/s11060-011-0727-x
Cited by 15
AI Summary: OriGene’s full-length human Bcl-2 cDNA clone (SC125546) was used in this study to overexpress Bcl-2 in glioma cells, enabling the investigation of its role in apoptosis following uPAR and cathepsin B downregulation.
Snippet: B (flC) (SC109129). For overexpression of Bcl-2, cells were transfected for 48 h with a plasmid expressing full-length human cDNA clone of Bcl-2 (flBcl-2) (SC125546) (OriGene Technologies, Inc. Rockville, MD). For the pCU
Showing 1-6 of 10 papers.
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