Mouse monoclonal mGFP/mCFP/mYFP/KillerRed antibody, clone OTI2F6

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TA180076
Mouse monoclonal mGFP/mCFP/mYFP/KillerRed antibody, clone OTI2F6
  $447.00
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Specifications
Specifications
Product Data
Clone Name OTI2F6 (formerly 2F6)
Application WB
Recommended Dilution WB: 1:500
Reactivity KillerRed, mCFP, mGFP, mYFP
Antibody Host Mouse
Clonality Monoclonal
Immunogen This antibody is raised against a recombinant protein of mGFP expressed in HEK293 cells. It recognizes mGFP, mCFP, mYFP and KillerRed proteins.
Isotype IgG1
Formulation PBS (pH 7.3) containing 1%BSA, 50% glycerol and 0.02% sodium azide
Concentration 1 mg/ml
Conjugation Unconjugated
Storage Store at -20°C.
Stability Stable for 1 year at -20°C from date of shipment.
Shipping Blue Ice
Predicted Protein Size 27.3 kDa
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Other "OTI2F6 (formerly 2F6)" antibodies (11)
SKU Description Size Price
CF180039 Carrier-free (BSA/glycerol-free) Mouse monoclonal mStrawberry antibody, clone OTI2F6 100 ug
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CF180076 Carrier-free (BSA/glycerol-free) Mouse monoclonal mGFP/mCFP/mYFP/KillerRed antibody, clone OTI2F6 100 ug
$620.00
TA180039 Mouse monoclonal mStrawberry antibody, clone OTI2F6 100 ul
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TA180039S Mouse monoclonal mStrawberry antibody, clone OTI2F6 30 ul
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TA180076S Mouse monoclonal mGFP/mCFP/mYFP/KillerRed antibody, clone OTI2F6 30 ul
$200.00
TA183010 Mouse monoclonal mStrawberry antibody, HRP conjugated 100 ul
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TA183015 Mouse monoclonal mGFP/mCFP/mYFP/KillerRed antibody, HRP conjugated 100 ul
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TA183033 Mouse Monoclonal mStrawberry Antibody, Magnetic Beads 1 ml
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TA183033S Mouse Monoclonal mStrawberry Antibody, Magnetic Beads 500 ul
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TA183038 Mouse Monoclonal mGFP/mCFP/mYFP/KillerRed Antibody, Magnetic Beads 1 ml
$776.00
TA183038S Mouse Monoclonal mGFP/mCFP/mYFP/KillerRed Antibody, Magnetic Beads 500 ul
$470.00

file-alt Citations

Retina-arrestin specific CD8+ T cells are not implicated in HLA-A29-positive birdshot chorioretinitis
Venema, Hiddingh, Janssen et al
Clin Immunol (2022) 247, 109219 DOI: 10.1016/j.clim.2022.109219
AI Summary: OriGene’s Lenti ORF clone of Human S-antigen mGFP tagged (RC220057L2) was used to engineer antigen-presenting cell lines to express retinal arrestin (SAG), enabling the study of naturally presented SAG peptides and their recognition by CD8+ T cells in birdshot chorioretinitis research.
Snippet: Background HLA-A29-positive birdshot chorioretinitis (BCR) is an inflammatory eye disorder that is generally assumed to be caused by an autoimmune response to HLA- Save;vector and 2.77 μg pMD2.G envelope vector at a ratio of 4:1) and 2 μg of the transfer vector (Lenti ORF clone of Human S-antigen mGFP tagged, RC220057L2, Origene) and cultured at 37 °C, 5% CO2 for 24 h. We replaced the medium with 10 mL DMEM supplemented with 10% FBS and collected the conditioned medium cont
ERAP2 Increases the Abundance of a Peptide Submotif Highly Selective for the Birdshot Uveitis-Associated HLA-A29
Venema, Hiddingh, de Boer et al
Front Immunol (2021) 12, 634441 DOI: 10.3389/fimmu.2021.634441
Cited by 33
AI Summary: In this study, OriGene’s ERAP2 (Cat# RC208361) and ERAP1 (Cat# RC209865) overexpression plasmids were used to manipulate ERAP2 and ERAP1 expression in patient-derived cells, enabling the authors to investigate how ERAP2 shapes the repertoire of peptides presented by HLA-A29 and its potential role in Birdshot Uveitis.
FigureFigureFigure
Clinical significance and functional role of transmembrane protein 47 (TMEM47) in chemoresistance of hepatocellular carcinoma
Ng, Yeung, Liu et al
Int J Oncol (2020) 57 (4), 956-966 DOI: 10.3892/ijo.2020.5104
Cited by 10
AI Summary: OriGene products, specifically the TMEM47 Human cDNA ORF Clone (Cat# RC210831) and TMEM47 shRNA plasmids (Cat# TG328631), were used in this study to manipulate TMEM47 expression in hepatocellular carcinoma cells, enabling the authors to investigate its role in chemoresistance.
FigureFigureFigure
Apical Sodium-Dependent Bile Acid Cotransporter, A Novel Transporter of Indocyanine Green, and Its Application in Drug Screening
Wu, Hsiao
Int J Mol Sci (2020) 21 (6) DOI: 10.3390/ijms21062202
Cited by 4
AI Summary: OriGene products RC210241L2 (ASBT) and RC221202L2 (NTCP) were used to generate lentiviruses for overexpressing these transporters in cells, enabling the study of their roles in indocyanine green transport and drug screening applications in this research.
Snippet: ASBT, NTCP, and GFP lentiviruses were made from RC210241L2 (Origene, Rockville, MD, USA), RC221202L2 (Origene, Rockville, MD, USA), and pCDH-EF1-MCS-BGH PGK-GFP-T2A-Puro (a generous gift from Dr. Yong-Chong Lin of National Taiwan University) Cached;- ASBT, NTCP, and GFP lentiviruses were made from RC210241L2 (Origene, Rockville, MD, USA), RC221202L2 (Origene, Rockville, MD, USA), and pCDH-EF1-MCS-BGH PGK-GFP-T2A-Puro (a generous gift from Dr. Yong-Chong Lin of National Taiwan University) Cached;- ASBT, NTCP, and GFP lentiviruses were made from RC210241L2 (Origene, Rockville, MD, USA), RC221202L2 (Origene, Rockville, MD, USA), and pCDH-EF1-MCS-BGH PGK-GFP-T2A-Puro (a generous gift from Dr. Yong-Chong Lin of National Taiwan University) Cached
FC
CTDP1 regulates breast cancer survival and DNA repair through BRCT-specific interactions with FANCI
Hu, Krieger, Lagundžin et al
Cell Death Discov (2019) 5, 105 DOI: 10.1038/s41420-019-0185-3
AI Summary: OriGene products contributed to this study by providing the full-length FANCI transcript variant 1 C-terminal fusion with monomeric GFP (mGFP) construct in pLenti-C-mGFP-P2A-Puro and the full-length CTDP1 transcript variant 1 C-terminal fusion with myc and DDK epitopes in pCMV6-Entry, which were used to investigate the molecular interactions and functions of CTDP1 and FANCI in breast cancer DNA repair mechanisms.
Snippet: … Full-length FANCI transcript variant 1 C-terminal fusion with monomeric GFP (mGFP) construct in pLenti-C-mGFP-P2A-Puro was purchased from Origene. …Full-length FANCI transcript variant 1 C-terminal fusion with monomeric GFP (mGFP) construct in pLenti-C-mGFP-P2A-Puro was purchased from Origene. …
FigureFigureFigure
TRIM8 regulates stemness in glioblastoma through PIAS3-STAT3
Zhang, Mukherjee, Tucker-Burden et al
Mol Oncol (2017) 11 (3), 280-294 DOI: 10.1002/1878-0261.12034
AI Summary: OriGene’s pLenti-TRIM8-mGFP TrueORF clone (RC205812L2) and pLenti-C-mGFP TrueORF clone (PS100071) were used to overexpress TRIM8 and as a vector control, respectively, enabling the study of TRIM8’s role in regulating stemness and STAT3 signaling in glioblastoma stem-like cells.
Snippet: TRIM8 cDNA was obtained from pLenti - TRIM8 - mGFP TrueORF clone (Origene#RC205812L2), with the vector control mGFP cDNA from pLenti - C - mGFP TrueORF clone (Origene#PS100071)
FigureFigureFigure
Showing 1-6 of 6 papers.
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