api 2000 mass spectrometer (electron spray ion source Search Results


98
Gatan Inc imaging filter gif 2000
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Otsuka Electronics Co Ltd photodiode array spectrometer mcpd 2000
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Scienta Omicron GmbH x-ray photo-electron spectroscopy vg scienta esca 2000
( a ) XRD data depending on the BP oxidation control. ( b ) XRD data of the dashed square in ( a ), highlighting the 32–36° peaks. ( c ) XRD data of OBP, 1T-WS 2 , 2H-WS 2 , and the nanocomposite. X-ray photoelectron spectra of ( d ) W 4f level and ( e ) P 2p level of 1T-WS 2 , OBP, and the nanocomposite.
X Ray Photo Electron Spectroscopy Vg Scienta Esca 2000, supplied by Scienta Omicron GmbH, 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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JEOL jsm 7100f 和透射电子显微镜
( a ) XRD data depending on the BP oxidation control. ( b ) XRD data of the dashed square in ( a ), highlighting the 32–36° peaks. ( c ) XRD data of OBP, 1T-WS 2 , 2H-WS 2 , and the nanocomposite. X-ray photoelectron spectra of ( d ) W 4f level and ( e ) P 2p level of 1T-WS 2 , OBP, and the nanocomposite.
Jsm 7100f 和透射电子显微镜, supplied by JEOL, used in various techniques. Bioz Stars score: 99/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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96
JASCO Inc nrs 5100 laser raman spectrometer
( a ) XRD data depending on the BP oxidation control. ( b ) XRD data of the dashed square in ( a ), highlighting the 32–36° peaks. ( c ) XRD data of OBP, 1T-WS 2 , 2H-WS 2 , and the nanocomposite. X-ray photoelectron spectra of ( d ) W 4f level and ( e ) P 2p level of 1T-WS 2 , OBP, and the nanocomposite.
Nrs 5100 Laser Raman Spectrometer, supplied by JASCO Inc, 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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90
ULVAC x-ray photoelectron spectroscopy system quantum 2000
( a ) XRD data depending on the BP oxidation control. ( b ) XRD data of the dashed square in ( a ), highlighting the 32–36° peaks. ( c ) XRD data of OBP, 1T-WS 2 , 2H-WS 2 , and the nanocomposite. X-ray photoelectron spectra of ( d ) W 4f level and ( e ) P 2p level of 1T-WS 2 , OBP, and the nanocomposite.
X Ray Photoelectron Spectroscopy System Quantum 2000, supplied by ULVAC, 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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ULVAC x-ray photoelectron spectroscopy quantum-2000
( a ) XRD data depending on the BP oxidation control. ( b ) XRD data of the dashed square in ( a ), highlighting the 32–36° peaks. ( c ) XRD data of OBP, 1T-WS 2 , 2H-WS 2 , and the nanocomposite. X-ray photoelectron spectra of ( d ) W 4f level and ( e ) P 2p level of 1T-WS 2 , OBP, and the nanocomposite.
X Ray Photoelectron Spectroscopy Quantum 2000, supplied by ULVAC, 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
Proteintech keap1
(A) Confocal images of MEFs that were starved for 3 h and stained for p62 and LC3. Scale bars: 10 μm. (B and C) Dot plots of the total p62 area (μm 2 ) (B) and global Pearson’s correlation coefficient of LC3 with p62 (C) in (A) ( n = 3). (D) Immunoblot analysis of 1% Triton X-100 (TX-100)-soluble and -insoluble fractions prepared from MEFs. (E) Bar plots of total p62, phosphorylated p62 (S405 and S351), and <t>KEAP1</t> in (D) ( n = 3). In (B), (C), and (E), statistical significance was determined by one-way ANOVA followed by Holm-Sidak’s multiple-comparisons test. All values in the bar graphs are mean ± SD. In (B) and (C), each dot represents the mean of each experiment ( n = 20 cells per experiment). * p ≤ 0.05, ** p ≤ 0.01, *** p ≤ 0.001, **** p ≤ 0.0001.
Keap1, 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
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90
ULVAC x-ray photoelectron spectrometer xps esca ulvac-phi 1600
(A) Confocal images of MEFs that were starved for 3 h and stained for p62 and LC3. Scale bars: 10 μm. (B and C) Dot plots of the total p62 area (μm 2 ) (B) and global Pearson’s correlation coefficient of LC3 with p62 (C) in (A) ( n = 3). (D) Immunoblot analysis of 1% Triton X-100 (TX-100)-soluble and -insoluble fractions prepared from MEFs. (E) Bar plots of total p62, phosphorylated p62 (S405 and S351), and <t>KEAP1</t> in (D) ( n = 3). In (B), (C), and (E), statistical significance was determined by one-way ANOVA followed by Holm-Sidak’s multiple-comparisons test. All values in the bar graphs are mean ± SD. In (B) and (C), each dot represents the mean of each experiment ( n = 20 cells per experiment). * p ≤ 0.05, ** p ≤ 0.01, *** p ≤ 0.001, **** p ≤ 0.0001.
X Ray Photoelectron Spectrometer Xps Esca Ulvac Phi 1600, supplied by ULVAC, 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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ULVAC quantum 2000 x-ray photoelectron spectroscopy apparatus
(A) Confocal images of MEFs that were starved for 3 h and stained for p62 and LC3. Scale bars: 10 μm. (B and C) Dot plots of the total p62 area (μm 2 ) (B) and global Pearson’s correlation coefficient of LC3 with p62 (C) in (A) ( n = 3). (D) Immunoblot analysis of 1% Triton X-100 (TX-100)-soluble and -insoluble fractions prepared from MEFs. (E) Bar plots of total p62, phosphorylated p62 (S405 and S351), and <t>KEAP1</t> in (D) ( n = 3). In (B), (C), and (E), statistical significance was determined by one-way ANOVA followed by Holm-Sidak’s multiple-comparisons test. All values in the bar graphs are mean ± SD. In (B) and (C), each dot represents the mean of each experiment ( n = 20 cells per experiment). * p ≤ 0.05, ** p ≤ 0.01, *** p ≤ 0.001, **** p ≤ 0.0001.
Quantum 2000 X Ray Photoelectron Spectroscopy Apparatus, supplied by ULVAC, 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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99
JEOL energy dispersive x ray spectrometer eds
(A) Confocal images of MEFs that were starved for 3 h and stained for p62 and LC3. Scale bars: 10 μm. (B and C) Dot plots of the total p62 area (μm 2 ) (B) and global Pearson’s correlation coefficient of LC3 with p62 (C) in (A) ( n = 3). (D) Immunoblot analysis of 1% Triton X-100 (TX-100)-soluble and -insoluble fractions prepared from MEFs. (E) Bar plots of total p62, phosphorylated p62 (S405 and S351), and <t>KEAP1</t> in (D) ( n = 3). In (B), (C), and (E), statistical significance was determined by one-way ANOVA followed by Holm-Sidak’s multiple-comparisons test. All values in the bar graphs are mean ± SD. In (B) and (C), each dot represents the mean of each experiment ( n = 20 cells per experiment). * p ≤ 0.05, ** p ≤ 0.01, *** p ≤ 0.001, **** p ≤ 0.0001.
Energy Dispersive X Ray Spectrometer Eds, supplied by JEOL, used in various techniques. Bioz Stars score: 99/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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86
Otsuka Electronics Co Ltd light scattering spectrometer
(A) Confocal images of MEFs that were starved for 3 h and stained for p62 and LC3. Scale bars: 10 μm. (B and C) Dot plots of the total p62 area (μm 2 ) (B) and global Pearson’s correlation coefficient of LC3 with p62 (C) in (A) ( n = 3). (D) Immunoblot analysis of 1% Triton X-100 (TX-100)-soluble and -insoluble fractions prepared from MEFs. (E) Bar plots of total p62, phosphorylated p62 (S405 and S351), and <t>KEAP1</t> in (D) ( n = 3). In (B), (C), and (E), statistical significance was determined by one-way ANOVA followed by Holm-Sidak’s multiple-comparisons test. All values in the bar graphs are mean ± SD. In (B) and (C), each dot represents the mean of each experiment ( n = 20 cells per experiment). * p ≤ 0.05, ** p ≤ 0.01, *** p ≤ 0.001, **** p ≤ 0.0001.
Light Scattering Spectrometer, supplied by Otsuka Electronics Co Ltd, used in various techniques. Bioz Stars score: 86/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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Image Search Results


( a ) XRD data depending on the BP oxidation control. ( b ) XRD data of the dashed square in ( a ), highlighting the 32–36° peaks. ( c ) XRD data of OBP, 1T-WS 2 , 2H-WS 2 , and the nanocomposite. X-ray photoelectron spectra of ( d ) W 4f level and ( e ) P 2p level of 1T-WS 2 , OBP, and the nanocomposite.

Journal: International Journal of Molecular Sciences

Article Title: P=O Functionalized Black Phosphorus/1T-WS 2 Nanocomposite High Efficiency Hybrid Photocatalyst for Air/Water Pollutant Degradation

doi: 10.3390/ijms23020733

Figure Lengend Snippet: ( a ) XRD data depending on the BP oxidation control. ( b ) XRD data of the dashed square in ( a ), highlighting the 32–36° peaks. ( c ) XRD data of OBP, 1T-WS 2 , 2H-WS 2 , and the nanocomposite. X-ray photoelectron spectra of ( d ) W 4f level and ( e ) P 2p level of 1T-WS 2 , OBP, and the nanocomposite.

Article Snippet: The surface composition and chemical state of the samples was evaluated by X-ray photo-electron spectroscopy (XPS) (Vg Scienta, Tonbridge, UK, ESCA 2000).

Techniques: Control

(A) Confocal images of MEFs that were starved for 3 h and stained for p62 and LC3. Scale bars: 10 μm. (B and C) Dot plots of the total p62 area (μm 2 ) (B) and global Pearson’s correlation coefficient of LC3 with p62 (C) in (A) ( n = 3). (D) Immunoblot analysis of 1% Triton X-100 (TX-100)-soluble and -insoluble fractions prepared from MEFs. (E) Bar plots of total p62, phosphorylated p62 (S405 and S351), and KEAP1 in (D) ( n = 3). In (B), (C), and (E), statistical significance was determined by one-way ANOVA followed by Holm-Sidak’s multiple-comparisons test. All values in the bar graphs are mean ± SD. In (B) and (C), each dot represents the mean of each experiment ( n = 20 cells per experiment). * p ≤ 0.05, ** p ≤ 0.01, *** p ≤ 0.001, **** p ≤ 0.0001.

Journal: Cell reports

Article Title: Unveiling the physiological impact of ESCRT-dependent autophagosome closure by targeting the VPS37A ubiquitin E2 variant-like domain

doi: 10.1016/j.celrep.2024.115016

Figure Lengend Snippet: (A) Confocal images of MEFs that were starved for 3 h and stained for p62 and LC3. Scale bars: 10 μm. (B and C) Dot plots of the total p62 area (μm 2 ) (B) and global Pearson’s correlation coefficient of LC3 with p62 (C) in (A) ( n = 3). (D) Immunoblot analysis of 1% Triton X-100 (TX-100)-soluble and -insoluble fractions prepared from MEFs. (E) Bar plots of total p62, phosphorylated p62 (S405 and S351), and KEAP1 in (D) ( n = 3). In (B), (C), and (E), statistical significance was determined by one-way ANOVA followed by Holm-Sidak’s multiple-comparisons test. All values in the bar graphs are mean ± SD. In (B) and (C), each dot represents the mean of each experiment ( n = 20 cells per experiment). * p ≤ 0.05, ** p ≤ 0.01, *** p ≤ 0.001, **** p ≤ 0.0001.

Article Snippet: The following primary antibodies were used for immunoblotting (IB), immunofluorescence (IF) and immunohistology (IH): mouse antibodies against α-tubulin (IB, T5168, 1:4000; Sigma-Aldrich), β-actin (IB, A5441, 1:10,000; Sigma-Aldrich), FLAG (IH, F1804, 1:500; Sigma-Aldrich), IκBα (IB, 1:1000; Cell Signaling Technology), LC3B (IH, M152–3, 1:200; MBL international), TSG101 (IB, GTX70255, 1:1,000; Genetex), Ubiquitin (NB300–130, 1:2000 for IB, 1:300 for IH; Novus), VPS28 (IB, sc-166537, 1:100; Santa Cruz Biotechnology); rabbit antibodies against Atg5 (IB, 12994, 1:1000; Cell Signaling Technology), Atg7 (IB, 8558, 1:1000; Cell Signaling Technology), Atg13 (IB, 13273, 1:1000; Cell Signaling Technology), EEA1 (IH, MA514794,1:200; Thermo Fisher Scientific), EGFR (IB, 4267, 1:1000; Cell Signaling Technology), GFP (IB, 2956, 1:1000; Cell Signaling Technology), Gstm1 (IB, 12412–1-AP, 1:1,000; Proteintech), HaloTag (IB, G928A, 1:1000; Promega), Iba1 (IH, 019–19741, 1:200; FUJIFILM Wako Pure Chemical Corporation), Keap1 (IB, 10503–2-AP, 1:2000; Proteintech), MAP1LC3B (IB, NB100–2220, 1:4000; Novus), MGST3 (IB, ab192254, 1:1000; Abcam), MVB12A (IB, 50–173-5082, 1:1,000; Fisher scientific), NQO1 (IB, 11451–1-AP, 1:2,000; Proteintech), NRF2 (IH, 12721, 1:200; Cell Signaling Technology), phospho-Atg13 Ser355 (IB, 46329, 1:1000; Cell Signaling Technology), phospho-p62 Ser349 (IB, 95697, 1:1000; Cell Signaling Technology), phospho-p62 Ser403 (IB, 39786, 1:1000; Cell Signaling Technology), phospho-TBK1 (5483, 1:1000 for IB, 1:200 for IH; Cell Signaling Technology), TBK1 (IB, 38066, 1:1000: Cell Signaling Technology), UBAP1 (IB, 12385–1-AP, 1:1,000; Proteintech), VPS37A (IB, HPA024705, 1:4000; Sigma-Aldrich; IB, 11870–1-AP, 1:2000; Proteintech); chicken antibody against GFAP (IH, CPCA-GFAP, 1:1000; EnCor Biotechnology); guinea pig antibodies against p62 (03-GP62-C, 1:4,000 for IB, 1:300 for IH; American Research Products); rat antibodies against CD11b (IH, MCA711, 1:200; Bio-Rad), LAMP1 (IH, sc-19992, 1:100; Santa Cruz Biotechnology); DyLight 650-conjugated NeutrAvidin (IH, 84607, 1:1000; Thermo Fisher Scientific).

Techniques: Staining, Western Blot

KEY RESOURCES TABLE

Journal: Cell reports

Article Title: Unveiling the physiological impact of ESCRT-dependent autophagosome closure by targeting the VPS37A ubiquitin E2 variant-like domain

doi: 10.1016/j.celrep.2024.115016

Figure Lengend Snippet: KEY RESOURCES TABLE

Article Snippet: The following primary antibodies were used for immunoblotting (IB), immunofluorescence (IF) and immunohistology (IH): mouse antibodies against α-tubulin (IB, T5168, 1:4000; Sigma-Aldrich), β-actin (IB, A5441, 1:10,000; Sigma-Aldrich), FLAG (IH, F1804, 1:500; Sigma-Aldrich), IκBα (IB, 1:1000; Cell Signaling Technology), LC3B (IH, M152–3, 1:200; MBL international), TSG101 (IB, GTX70255, 1:1,000; Genetex), Ubiquitin (NB300–130, 1:2000 for IB, 1:300 for IH; Novus), VPS28 (IB, sc-166537, 1:100; Santa Cruz Biotechnology); rabbit antibodies against Atg5 (IB, 12994, 1:1000; Cell Signaling Technology), Atg7 (IB, 8558, 1:1000; Cell Signaling Technology), Atg13 (IB, 13273, 1:1000; Cell Signaling Technology), EEA1 (IH, MA514794,1:200; Thermo Fisher Scientific), EGFR (IB, 4267, 1:1000; Cell Signaling Technology), GFP (IB, 2956, 1:1000; Cell Signaling Technology), Gstm1 (IB, 12412–1-AP, 1:1,000; Proteintech), HaloTag (IB, G928A, 1:1000; Promega), Iba1 (IH, 019–19741, 1:200; FUJIFILM Wako Pure Chemical Corporation), Keap1 (IB, 10503–2-AP, 1:2000; Proteintech), MAP1LC3B (IB, NB100–2220, 1:4000; Novus), MGST3 (IB, ab192254, 1:1000; Abcam), MVB12A (IB, 50–173-5082, 1:1,000; Fisher scientific), NQO1 (IB, 11451–1-AP, 1:2,000; Proteintech), NRF2 (IH, 12721, 1:200; Cell Signaling Technology), phospho-Atg13 Ser355 (IB, 46329, 1:1000; Cell Signaling Technology), phospho-p62 Ser349 (IB, 95697, 1:1000; Cell Signaling Technology), phospho-p62 Ser403 (IB, 39786, 1:1000; Cell Signaling Technology), phospho-TBK1 (5483, 1:1000 for IB, 1:200 for IH; Cell Signaling Technology), TBK1 (IB, 38066, 1:1000: Cell Signaling Technology), UBAP1 (IB, 12385–1-AP, 1:1,000; Proteintech), VPS37A (IB, HPA024705, 1:4000; Sigma-Aldrich; IB, 11870–1-AP, 1:2000; Proteintech); chicken antibody against GFAP (IH, CPCA-GFAP, 1:1000; EnCor Biotechnology); guinea pig antibodies against p62 (03-GP62-C, 1:4,000 for IB, 1:300 for IH; American Research Products); rat antibodies against CD11b (IH, MCA711, 1:200; Bio-Rad), LAMP1 (IH, sc-19992, 1:100; Santa Cruz Biotechnology); DyLight 650-conjugated NeutrAvidin (IH, 84607, 1:1000; Thermo Fisher Scientific).

Techniques: Ubiquitin Proteomics, Recombinant, Modification, Membrane, Electron Microscopy, Protease Inhibitor, Clinical Proteomics, Enzyme-linked Immunosorbent Assay, Mass Spectrometry, Plasmid Preparation, Software, Imaging