Rabbit Polyclonal turboGFP Antibody
$377.00
In Stock*
Specifications
| Product Data | |
| Application | WB |
|---|---|
| Recommended Dilution | WB: 1:2000 |
| Reactivity | tGFP |
| Antibody Host | Rabbit |
| Clonality | Polyclonal |
| Immunogen | Purified tGFP protein expressed in E. coli. |
| Isotype | IgG |
| Formulation | Whole antiserum; preservative: 0.05% Sodium azide |
| Concentration | This antibody is provided as whole antiserum. The exact antibody concentration is hard to determine. |
| Conjugation | Unconjugated |
| Storage | Store at -20°C. For maximum recovery of product, centrifuge the original vial after thawing and prior to opening the cap. Aliquot to avoid repeated freezing and thawing. |
| Stability | Stable for 1 year at -20°C from date of shipment. |
| Shipping | Blue Ice |
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Citations
VPS35 mutation inhibits PINK1/parkin-mediated mitophagy via increased LRRK2 kinase activity
Manders, Heyninck, Imberechts et al
Brain (2025)
Manders, Heyninck, Imberechts et al
Brain (2025)
Cited by 6
In vivo single-cell CRISPR screening for microproteins identifies a critical ribosomal component
Valdivia-Francia, Ghoshdastider, Renz et al
bioRxiv (2025)
Valdivia-Francia, Ghoshdastider, Renz et al
bioRxiv (2025)
Cited by 3
AI Summary: In this study, the Anti-turboGFP Rabbit polyclonal antibody (OriGene TA150071) was used to detect turboGFP-tagged proteins, facilitating the analysis of microprotein function in the single-cell CRISPR screening experiments.
Snippet: …The following antibodies were used: Anti-turboGFP Rabbit polyclonal antibody (ORIGENE TA150071), PTEN (138G6) rabbit mAB (Cell signaling #9559), Actin (8H10D10) mAB (Thermo Scientific MA5-15452), Cas9 (7A9-3A3) mouse mAb (Cell signaling #1497), Anti-rabbit IgG HRPlinked antibody (Cell signaling #7074) and Anti-mouse IgG HRP-linked antibody (Cell signaling #7076)
SMURF2 facilitates GAP17 Isoform 1 membrane displacement to promote mutant p53-KRAS oncogenic synergy
Ray, Shukla, Zhang et al
Mol Cancer Res (2025)
Ray, Shukla, Zhang et al
Mol Cancer Res (2025)
AI Summary: OriGene’s Turbo GFP antibody (Cat# TA150071) was used in this study to detect GFP-tagged proteins, aiding in the analysis of protein localization and interactions relevant to SMURF2-mediated GAP17-1 membrane displacement in pancreatic cancer models.
Snippet: from Sigma (St Louis, MO). Turbo GFP antibody (Cat# TA150071, RRID: AB_2622256) was purchased from Origene (Rockville, MD, RRID: SCR_008985). Control (Cat# D-001810), SMURF2 (Cat# D-007194), UBE2L3 (Cat# L-010384) and UBE2D1 (Cat# J-009387) small interfering RNA (siRNA) were purchased from ThermoFisher Sci
Brain-Homing Peptide Expression on the Membrane Enhances the Delivery of Exosomes to Neural Cells and Tissue
Smith, Field, Sugaya
Neuroglia (2025) 6 (1), 3-3 DOI: 10.3390/neuroglia6010003
Smith, Field, Sugaya
Neuroglia (2025) 6 (1), 3-3 DOI: 10.3390/neuroglia6010003
Cited by 4
AI Summary: OriGene’s TurboGFP antibody (Cat: TA150071) was used in this study to detect and quantify GFP cargo delivery by engineered exosomes, thereby enabling the assessment of exosome targeting efficiency to neural cells and tissue.
Snippet: … Before blocking, the PVDF membrane was activated by pre-wetting in 100% methanol for 1 min, followed by soaking in ddH2O for 2 min and then in TBST for 5 min. TurboGFP (Origene, Rockville, MD, USA, Cat: TA150071) and β-Actin (Cell Signaling, Danvers, MA, USA, Cat: 4970L) primary antibodies were diluted in the blocking solution at 1:2000 and 1:4000 concentration, respectively, and incubated overnight at 4 °
O-GlcNAcylation of irf3 by a novel Zebrafish O-GlcNAc transferase isoform Ogtb_tv3 facilitates its sufficient activation and innate antiviral response
LU, Aoling, Jie et al
Research Square (2024)
LU, Aoling, Jie et al
Research Square (2024)
Snippet: Protein complexes were incubated overnight at 4°C with agarose-bound anti-FLAG antibody (AE095;Abclonal) with gentle agitation. Post-incubation, beads were washed and proteins eluted for immunoblot analysis using anti-FLAG and anti-pTurboGFP (TA150071;Origene) antibodies
Ca+2 and Nε-lysine acetylation regulate the CALR-ATG9A interaction in the lumen of the endoplasmic reticulum
Braun, Sheehan, Shapiro et al
Sci Rep (2024) 14 (1), 25532 DOI: 10.1038/s41598-024-76854-4
Braun, Sheehan, Shapiro et al
Sci Rep (2024) 14 (1), 25532 DOI: 10.1038/s41598-024-76854-4
Cited by 1
AI Summary: OriGene products contributed to this study by providing primary antibodies (DDK, TA100011; tGFP, TA150071) and expression plasmids (pCMV6-SERCA-DDK, RC207626; pCMV6-ITPR3-DDK, RC222737; pCMV6-ATG9A-DDK, RC222513; pCMV6-ATG9A-tGFP, RG222568; pCMV6-CALR-DDK, RC203222) that were essential for detecting and expressing key proteins involved in investigating the regulation of ATG9A-CALR interactions in the endoplasmic reticulum.
Snippet: The following primary antibodies were used in this study: DDK (Origene, TA100011, 1:1000), ITPR3 (abcam, ab264283, 1:2000), tGFP (Origene, TA150071, 1:1000), and;itrogen, 2773051) and MEFs were transiently transfected with Lipofectamine STEM (Invitrogen, 01108889), according to manufacturer’s recommendations. Commercial plasmids used: human pCMV6-SERCA-DDK (Origene, RC207626), human pCMV6-ITPR3-DDK (Origene, RC222737), human pCMV6-ATG9A-DDK (Origene, RC222513), human pCMV6-ATG9A-tGFP (Origene, RG222568), human pCMV6-CALR-DDK (Origene, RC203222), ER signa
Showing 1-6 of 13 papers.
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