1 ig 7 Search Results


96
Vector Laboratories biotinylated horse anti mouse ig
Biotinylated Horse Anti Mouse Ig, supplied by Vector Laboratories, used in various techniques. Bioz Stars score: 96/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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biotinylated horse anti mouse ig - by Bioz Stars, 2026-03
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94
Proteintech 1 ig 7
1 Ig 7, supplied by Proteintech, used in various techniques. Bioz Stars score: 94/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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Average 94 stars, based on 1 article reviews
1 ig 7 - by Bioz Stars, 2026-03
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90
Abnova pcna ig7
Pcna Ig7, supplied by Abnova, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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Average 90 stars, based on 1 article reviews
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93
Proteintech apex1 proteintech 67781 1 ig 7 dna polymerase beta
Apex1 Proteintech 67781 1 Ig 7 Dna Polymerase Beta, supplied by Proteintech, used in various techniques. Bioz Stars score: 93/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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Average 93 stars, based on 1 article reviews
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96
Proteintech gfp
Targeted <t>GFP</t> 1–10 sensors reveal subcellular pools of Tau. ( a ) The subcellular distribution of the indicated GFP 1–10 sensors in transiently transfected mouse C17.2 cells is shown by confocal microscopy upon immune staining of PFA-fixed cells with <t>an</t> <t>anti-GFP</t> antibody (upper row, in red). The cells are counter-stained with the ER-marker calnexin (middle row, in cyan) and the nuclear stain DAPI (shown in the merged images, bottom row, in blue). ( b ) The GFP 1–10 sensors were then co-transfected with S 11 -Tau, which reveals by biFC biofluorescence (upper row, in green) microtubule-associated Tau with GFP 1–10 , nuclear Tau with nucGFP 1–10 , and mitochondria-associated Tau with ommGFP 1–10 . No biFC is obtained with the erGFP 1–10 sensor, unless Tau is targeted to the ER lumen (erTau-S 11 , column on the far right). The cells are counter-stained for total human Tau with the Tau13 antibody (middle row, in red) and DAPI (merged images, bottom row, in blue).
Gfp, supplied by Proteintech, used in various techniques. Bioz Stars score: 96/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/result/gfp/product/Proteintech
Average 96 stars, based on 1 article reviews
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96/100 stars
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90
Santa Cruz Biotechnology anti-ifi16 (ig7)
Targeted <t>GFP</t> 1–10 sensors reveal subcellular pools of Tau. ( a ) The subcellular distribution of the indicated GFP 1–10 sensors in transiently transfected mouse C17.2 cells is shown by confocal microscopy upon immune staining of PFA-fixed cells with <t>an</t> <t>anti-GFP</t> antibody (upper row, in red). The cells are counter-stained with the ER-marker calnexin (middle row, in cyan) and the nuclear stain DAPI (shown in the merged images, bottom row, in blue). ( b ) The GFP 1–10 sensors were then co-transfected with S 11 -Tau, which reveals by biFC biofluorescence (upper row, in green) microtubule-associated Tau with GFP 1–10 , nuclear Tau with nucGFP 1–10 , and mitochondria-associated Tau with ommGFP 1–10 . No biFC is obtained with the erGFP 1–10 sensor, unless Tau is targeted to the ER lumen (erTau-S 11 , column on the far right). The cells are counter-stained for total human Tau with the Tau13 antibody (middle row, in red) and DAPI (merged images, bottom row, in blue).
Anti Ifi16 (Ig7), supplied by Santa Cruz Biotechnology, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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Average 90 stars, based on 1 article reviews
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90
NutraBio Labs Inc nac
Studies included in the systematic review of the effect of N-Acetylcysteine supplementation on health biomarkers.
Nac, supplied by NutraBio Labs Inc, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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Average 90 stars, based on 1 article reviews
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90
Agilent technologies 1-antitrypsin
Studies included in the systematic review of the effect of N-Acetylcysteine supplementation on health biomarkers.
1 Antitrypsin, supplied by Agilent technologies, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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96
Jackson Immuno donkey anti rabbit ig
Studies included in the systematic review of the effect of N-Acetylcysteine supplementation on health biomarkers.
Donkey Anti Rabbit Ig, supplied by Jackson Immuno, used in various techniques. Bioz Stars score: 96/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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96
Vector Laboratories biotinylated goat anti rabbit ig
Studies included in the systematic review of the effect of N-Acetylcysteine supplementation on health biomarkers.
Biotinylated Goat Anti Rabbit Ig, supplied by Vector Laboratories, used in various techniques. Bioz Stars score: 96/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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Average 96 stars, based on 1 article reviews
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N/A
Monkey primate IGFBP7/Igfbp Rp1 ELISA Kit PicoKine® (96 Tests). Quantitate Monkey IGFBP7 in cell culture supernatants, serum, plasma (heparin, EDTA) and urine. Sensitivity: 20pg/ml. The brand Picokine indicates this is a premium quality ELISA kit.
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Image Search Results


Targeted GFP 1–10 sensors reveal subcellular pools of Tau. ( a ) The subcellular distribution of the indicated GFP 1–10 sensors in transiently transfected mouse C17.2 cells is shown by confocal microscopy upon immune staining of PFA-fixed cells with an anti-GFP antibody (upper row, in red). The cells are counter-stained with the ER-marker calnexin (middle row, in cyan) and the nuclear stain DAPI (shown in the merged images, bottom row, in blue). ( b ) The GFP 1–10 sensors were then co-transfected with S 11 -Tau, which reveals by biFC biofluorescence (upper row, in green) microtubule-associated Tau with GFP 1–10 , nuclear Tau with nucGFP 1–10 , and mitochondria-associated Tau with ommGFP 1–10 . No biFC is obtained with the erGFP 1–10 sensor, unless Tau is targeted to the ER lumen (erTau-S 11 , column on the far right). The cells are counter-stained for total human Tau with the Tau13 antibody (middle row, in red) and DAPI (merged images, bottom row, in blue).

Journal: Scientific Reports

Article Title: Phosphorylation of nuclear Tau is modulated by distinct cellular pathways

doi: 10.1038/s41598-018-36374-4

Figure Lengend Snippet: Targeted GFP 1–10 sensors reveal subcellular pools of Tau. ( a ) The subcellular distribution of the indicated GFP 1–10 sensors in transiently transfected mouse C17.2 cells is shown by confocal microscopy upon immune staining of PFA-fixed cells with an anti-GFP antibody (upper row, in red). The cells are counter-stained with the ER-marker calnexin (middle row, in cyan) and the nuclear stain DAPI (shown in the merged images, bottom row, in blue). ( b ) The GFP 1–10 sensors were then co-transfected with S 11 -Tau, which reveals by biFC biofluorescence (upper row, in green) microtubule-associated Tau with GFP 1–10 , nuclear Tau with nucGFP 1–10 , and mitochondria-associated Tau with ommGFP 1–10 . No biFC is obtained with the erGFP 1–10 sensor, unless Tau is targeted to the ER lumen (erTau-S 11 , column on the far right). The cells are counter-stained for total human Tau with the Tau13 antibody (middle row, in red) and DAPI (merged images, bottom row, in blue).

Article Snippet: Primary antibodies, usually incubated for 1 h at 37 °C, were specific for human Tau (Tau13, Santa Cruz, sc-21796, used at 1 μg/mL), GFP (Proteintech Europe, 66002–1-Ig, 7 μg/mL), calnexin (kind gift of Prof. Maurizio Molinari, IRB, Bellinzona, Switzerland, diluted 1:1,000), α-tubulin (Abcam, ab1825, 0.5 μg/mL or Cell Signaling, DM1A, diluted 1:500), pS 129 -H2A.X (Santa Cruz, sc-517348, 0.5 μg/mL), pATM (Cell Signaling, S1981, diluted 1:500), pChk1 (Cell Signaling, S345, diluted 1:500), pChk2 (Cell Signaling, T68, diluted 1:500), pATR (Cell Signaling, S428, diluted 1:500).

Techniques: Transfection, Confocal Microscopy, Staining, Marker

Immune isolation of Tau by mean of the GFP 1–10 sensors. ( a ) Cell lysates from C17.2 cells transfected as indicated are analysed by western blot before (cell lysates) or after immune isolation on anti-GFP magnetic beads (GFP-Trap isolates). This shows specific isolation of S 11 -Tau when co-transfected with GFP 1–10 , but not in the negative controls, including post-lysis mixing of lysates obtained from cells transfected with either S 11 -Tau or GFP 1–10 (lanes labelled with “mix”). β-actin is the loading control for the cell lysates, whereas the presence of the sensor is verified with an anti-GFP antibody. ( b ) Cell lysates and GFP-immune isolates obtained from C17.2 cells transiently transfected with S 11 -Tau and the indicated sensors are analysed by western blot as described for ( a ). Molecular weight markers are given on the left of the blots, full blots are shown scanned by dual infrared imaging.

Journal: Scientific Reports

Article Title: Phosphorylation of nuclear Tau is modulated by distinct cellular pathways

doi: 10.1038/s41598-018-36374-4

Figure Lengend Snippet: Immune isolation of Tau by mean of the GFP 1–10 sensors. ( a ) Cell lysates from C17.2 cells transfected as indicated are analysed by western blot before (cell lysates) or after immune isolation on anti-GFP magnetic beads (GFP-Trap isolates). This shows specific isolation of S 11 -Tau when co-transfected with GFP 1–10 , but not in the negative controls, including post-lysis mixing of lysates obtained from cells transfected with either S 11 -Tau or GFP 1–10 (lanes labelled with “mix”). β-actin is the loading control for the cell lysates, whereas the presence of the sensor is verified with an anti-GFP antibody. ( b ) Cell lysates and GFP-immune isolates obtained from C17.2 cells transiently transfected with S 11 -Tau and the indicated sensors are analysed by western blot as described for ( a ). Molecular weight markers are given on the left of the blots, full blots are shown scanned by dual infrared imaging.

Article Snippet: Primary antibodies, usually incubated for 1 h at 37 °C, were specific for human Tau (Tau13, Santa Cruz, sc-21796, used at 1 μg/mL), GFP (Proteintech Europe, 66002–1-Ig, 7 μg/mL), calnexin (kind gift of Prof. Maurizio Molinari, IRB, Bellinzona, Switzerland, diluted 1:1,000), α-tubulin (Abcam, ab1825, 0.5 μg/mL or Cell Signaling, DM1A, diluted 1:500), pS 129 -H2A.X (Santa Cruz, sc-517348, 0.5 μg/mL), pATM (Cell Signaling, S1981, diluted 1:500), pChk1 (Cell Signaling, S345, diluted 1:500), pChk2 (Cell Signaling, T68, diluted 1:500), pATR (Cell Signaling, S428, diluted 1:500).

Techniques: Isolation, Transfection, Western Blot, Magnetic Beads, Lysis, Control, Molecular Weight, Imaging

Studies included in the systematic review of the effect of N-Acetylcysteine supplementation on health biomarkers.

Journal: Nutrients

Article Title: Influence of N-Acetylcysteine Supplementation on Physical Performance and Laboratory Biomarkers in Adult Males: A Systematic Review of Controlled Trials

doi: 10.3390/nu15112463

Figure Lengend Snippet: Studies included in the systematic review of the effect of N-Acetylcysteine supplementation on health biomarkers.

Article Snippet: Rhodes et al, 2019, Australia [ ] , Double-blind, pre-post, placebo-controlled , 17 ♂ Semi-professional/Semi-elite rugby players Age (mean ± SD) 20.4 ± 0.9 years Weight (mean ± SD) 103.0 ± 12.0 kg Height (mean ± SD) 182.3 ± 7.4 cm Yo-Yo Intermittent Recovery Test Level 1 (mean ± SD) 17.4 ± 1.73 Level Study withdrawals: 4 6 participants IG 7 participants CG , IG: 1 g/day (2 × 50 mg capsules) NAC (Nutrabio Labs Inc., Middlesex, NJ, USA) CG: 1 g (2 × 50 mg capsules) of placebo (sucrose and salt mixture) For 6 days. , Muscle soreness Broken bronco shuttle test Fastest shuttle time (High-intensity exercise) Side effects , ↑ Muscle Soreness ↔ Broken bronco shuttle test ↑ Fastest shuttle time ↔ Side Effects.

Techniques: Activity Assay, Nitration