10-beta Search Results


99
New England Biolabs 10 beta competent cells
10 Beta Competent Cells, supplied by New England Biolabs, 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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91
R&D Systems recombiant integrin α10β1 protein

Recombiant Integrin α10β1 Protein, supplied by R&D Systems, used in various techniques. Bioz Stars score: 91/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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96
New England Biolabs e coli

E Coli, supplied by New England Biolabs, 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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New England Biolabs neb 10 beta electrocompetent cells

Neb 10 Beta Electrocompetent Cells, supplied by New England Biolabs, 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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New England Biolabs virus strains 10 beta competent e coli new england biolabs catalog

Virus Strains 10 Beta Competent E Coli New England Biolabs Catalog, supplied by New England Biolabs, 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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New England Biolabs neb10β outgrowth medium

Neb10β Outgrowth Medium, supplied by New England Biolabs, 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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New England Biolabs neb 10 beta

Neb 10 Beta, supplied by New England Biolabs, 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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Lee Biosolutions human urine

Human Urine, supplied by Lee Biosolutions, 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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Lee Biosolutions b2m
Identification of <t>B2M</t> as antimicrobial active molecule in BAL fluid by mass spectrometry. A (left): Electrospray-mass spectrum of antimicrobial fraction 57 showing multiple charged states for B2M. Right: Mass isotope pattern of antimicrobial fraction Fr57 at z = 11. B (left): Theoretical multiply-charged ions spectrum of mature B2M (UniprotKB-P61769, 21–119). Right: Theoretical mass isotope pattern of B2M (UniprotKB-P61769, 21–119) at z = 11. Both, the mass/charge state distributions and isotope pattern (z = 11) of fraction 57 (Figure 2(a)) match the respective simulated ones of mature B2M (Figure 2(b)). The calculated average masses are very close: 11,729.41 Da (experimental) vs. 11,729.15 Da (theoretical, from ProtParam). C : MS/MS fragmentation spectrum of a B2M proteolytic fragment, corresponding to the sequence IEKVEHSDLSFSK. D : Sequence coverage (93%) by sequencing of digested B2M. Delimited blue horizontal bars represent every proteolytic fragment identified in the sequence. Vertical red bars/squares represent a Cys residue identified as carbamidomethylated. Numbers at both sides of the figure represent the residue position in the precursor sequence. The sequence delimited by arrows represents the signal peptide (UniprotKB-P61769, 1–20)
B2m, supplied by Lee Biosolutions, used in various techniques. Bioz Stars score: 91/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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86
ChromaDex docetaxel dtx
Identification of <t>B2M</t> as antimicrobial active molecule in BAL fluid by mass spectrometry. A (left): Electrospray-mass spectrum of antimicrobial fraction 57 showing multiple charged states for B2M. Right: Mass isotope pattern of antimicrobial fraction Fr57 at z = 11. B (left): Theoretical multiply-charged ions spectrum of mature B2M (UniprotKB-P61769, 21–119). Right: Theoretical mass isotope pattern of B2M (UniprotKB-P61769, 21–119) at z = 11. Both, the mass/charge state distributions and isotope pattern (z = 11) of fraction 57 (Figure 2(a)) match the respective simulated ones of mature B2M (Figure 2(b)). The calculated average masses are very close: 11,729.41 Da (experimental) vs. 11,729.15 Da (theoretical, from ProtParam). C : MS/MS fragmentation spectrum of a B2M proteolytic fragment, corresponding to the sequence IEKVEHSDLSFSK. D : Sequence coverage (93%) by sequencing of digested B2M. Delimited blue horizontal bars represent every proteolytic fragment identified in the sequence. Vertical red bars/squares represent a Cys residue identified as carbamidomethylated. Numbers at both sides of the figure represent the residue position in the precursor sequence. The sequence delimited by arrows represents the signal peptide (UniprotKB-P61769, 1–20)
Docetaxel Dtx, supplied by ChromaDex, 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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90
Echelon Biosciences powder
Identification of <t>B2M</t> as antimicrobial active molecule in BAL fluid by mass spectrometry. A (left): Electrospray-mass spectrum of antimicrobial fraction 57 showing multiple charged states for B2M. Right: Mass isotope pattern of antimicrobial fraction Fr57 at z = 11. B (left): Theoretical multiply-charged ions spectrum of mature B2M (UniprotKB-P61769, 21–119). Right: Theoretical mass isotope pattern of B2M (UniprotKB-P61769, 21–119) at z = 11. Both, the mass/charge state distributions and isotope pattern (z = 11) of fraction 57 (Figure 2(a)) match the respective simulated ones of mature B2M (Figure 2(b)). The calculated average masses are very close: 11,729.41 Da (experimental) vs. 11,729.15 Da (theoretical, from ProtParam). C : MS/MS fragmentation spectrum of a B2M proteolytic fragment, corresponding to the sequence IEKVEHSDLSFSK. D : Sequence coverage (93%) by sequencing of digested B2M. Delimited blue horizontal bars represent every proteolytic fragment identified in the sequence. Vertical red bars/squares represent a Cys residue identified as carbamidomethylated. Numbers at both sides of the figure represent the residue position in the precursor sequence. The sequence delimited by arrows represents the signal peptide (UniprotKB-P61769, 1–20)
Powder, supplied by Echelon Biosciences, 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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95
Chem Impex International paclitaxel
Identification of <t>B2M</t> as antimicrobial active molecule in BAL fluid by mass spectrometry. A (left): Electrospray-mass spectrum of antimicrobial fraction 57 showing multiple charged states for B2M. Right: Mass isotope pattern of antimicrobial fraction Fr57 at z = 11. B (left): Theoretical multiply-charged ions spectrum of mature B2M (UniprotKB-P61769, 21–119). Right: Theoretical mass isotope pattern of B2M (UniprotKB-P61769, 21–119) at z = 11. Both, the mass/charge state distributions and isotope pattern (z = 11) of fraction 57 (Figure 2(a)) match the respective simulated ones of mature B2M (Figure 2(b)). The calculated average masses are very close: 11,729.41 Da (experimental) vs. 11,729.15 Da (theoretical, from ProtParam). C : MS/MS fragmentation spectrum of a B2M proteolytic fragment, corresponding to the sequence IEKVEHSDLSFSK. D : Sequence coverage (93%) by sequencing of digested B2M. Delimited blue horizontal bars represent every proteolytic fragment identified in the sequence. Vertical red bars/squares represent a Cys residue identified as carbamidomethylated. Numbers at both sides of the figure represent the residue position in the precursor sequence. The sequence delimited by arrows represents the signal peptide (UniprotKB-P61769, 1–20)
Paclitaxel, supplied by Chem Impex International, used in various techniques. Bioz Stars score: 95/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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Image Search Results


Journal: eLife

Article Title: Integrin alpha11 is an Osteolectin receptor and is required for the maintenance of adult skeletal bone mass

doi: 10.7554/eLife.42274

Figure Lengend Snippet:

Article Snippet: Peptide, recombinant protein , recombiant Integrin α10β1 protein , R and D Systems , 5895-AB , .

Techniques: Recombinant, Diagnostic Assay, Cell Culture, Protease Inhibitor, Western Blot, Reverse Transcription, Enzyme-linked Immunosorbent Assay, Fractionation

Journal: STAR Protocols

Article Title: Protocol for establishing inducible CRISPR interference system for multiple-gene silencing in human pluripotent stem cells

doi: 10.1016/j.xpro.2024.103221

Figure Lengend Snippet:

Article Snippet: Add 950 μL of NEB 10-beta/Stable Outgrowth Medium to the mixture. x.

Techniques: Virus, Recombinant, Knock-Out, Membrane, Gentle, Infection, Gel Extraction, Plasmid Preparation, TaqMan Copy Number Assay, Lysis, SYBR Green Assay, Software

Identification of B2M as antimicrobial active molecule in BAL fluid by mass spectrometry. A (left): Electrospray-mass spectrum of antimicrobial fraction 57 showing multiple charged states for B2M. Right: Mass isotope pattern of antimicrobial fraction Fr57 at z = 11. B (left): Theoretical multiply-charged ions spectrum of mature B2M (UniprotKB-P61769, 21–119). Right: Theoretical mass isotope pattern of B2M (UniprotKB-P61769, 21–119) at z = 11. Both, the mass/charge state distributions and isotope pattern (z = 11) of fraction 57 (Figure 2(a)) match the respective simulated ones of mature B2M (Figure 2(b)). The calculated average masses are very close: 11,729.41 Da (experimental) vs. 11,729.15 Da (theoretical, from ProtParam). C : MS/MS fragmentation spectrum of a B2M proteolytic fragment, corresponding to the sequence IEKVEHSDLSFSK. D : Sequence coverage (93%) by sequencing of digested B2M. Delimited blue horizontal bars represent every proteolytic fragment identified in the sequence. Vertical red bars/squares represent a Cys residue identified as carbamidomethylated. Numbers at both sides of the figure represent the residue position in the precursor sequence. The sequence delimited by arrows represents the signal peptide (UniprotKB-P61769, 1–20)

Journal: Virulence

Article Title: Respiratory ß-2-Microglobulin exerts pH dependent antimicrobial activity

doi: 10.1080/21505594.2020.1831367

Figure Lengend Snippet: Identification of B2M as antimicrobial active molecule in BAL fluid by mass spectrometry. A (left): Electrospray-mass spectrum of antimicrobial fraction 57 showing multiple charged states for B2M. Right: Mass isotope pattern of antimicrobial fraction Fr57 at z = 11. B (left): Theoretical multiply-charged ions spectrum of mature B2M (UniprotKB-P61769, 21–119). Right: Theoretical mass isotope pattern of B2M (UniprotKB-P61769, 21–119) at z = 11. Both, the mass/charge state distributions and isotope pattern (z = 11) of fraction 57 (Figure 2(a)) match the respective simulated ones of mature B2M (Figure 2(b)). The calculated average masses are very close: 11,729.41 Da (experimental) vs. 11,729.15 Da (theoretical, from ProtParam). C : MS/MS fragmentation spectrum of a B2M proteolytic fragment, corresponding to the sequence IEKVEHSDLSFSK. D : Sequence coverage (93%) by sequencing of digested B2M. Delimited blue horizontal bars represent every proteolytic fragment identified in the sequence. Vertical red bars/squares represent a Cys residue identified as carbamidomethylated. Numbers at both sides of the figure represent the residue position in the precursor sequence. The sequence delimited by arrows represents the signal peptide (UniprotKB-P61769, 1–20)

Article Snippet: 90 μl of the bacterial suspension was mixed with 10 μl of the desired concentration of B2M (Lee BioSolutions, St. Louis, Missouri, 126–12-10) or with 10 μl of ddH 2 O (negative control) followed by incubation at 37°C.

Techniques: Mass Spectrometry, Tandem Mass Spectroscopy, Sequencing, Residue

Antibacterial activity of purified B2M. The dose-dependent antibacterial activity of B2M was tested in a radial diffusion assay against the screening strains B. subtilis and P. aeruginosa (a), and against L. monocytogenes (b). The mean value and standard deviation for three independent experiments is depicted

Journal: Virulence

Article Title: Respiratory ß-2-Microglobulin exerts pH dependent antimicrobial activity

doi: 10.1080/21505594.2020.1831367

Figure Lengend Snippet: Antibacterial activity of purified B2M. The dose-dependent antibacterial activity of B2M was tested in a radial diffusion assay against the screening strains B. subtilis and P. aeruginosa (a), and against L. monocytogenes (b). The mean value and standard deviation for three independent experiments is depicted

Article Snippet: 90 μl of the bacterial suspension was mixed with 10 μl of the desired concentration of B2M (Lee BioSolutions, St. Louis, Missouri, 126–12-10) or with 10 μl of ddH 2 O (negative control) followed by incubation at 37°C.

Techniques: Activity Assay, Purification, Diffusion-based Assay, Standard Deviation

pH-dependent antibacterial activity of purified B2M against L. monocytogenes . A : Amyloidogenic potential of B2M at low pH conditions. The presence of amyloid fibrils was monitored by ThT staining. B2M was either subjected directly to ThT measurement or was incubated at 37°C for 30 min in buffer with the indicated pH. EF-C fibrils served as positive control (pos control). The mean value and standard deviation for two independent experiments is depicted. B : Antibacterial activity of B2M was tested in radial diffusion assays using pH modified agarose solutions (4.5 to 7). Antibacterial activity of B2M in radial diffusion assays could only be observed at pH values lower than 6. C : The pH-dependent effect of B2M (1 mg/ml) against L. monocytogenes in a survival assay. Peptide and mock-treated bacteria were incubated at pH values 7, 5.5 and 4.5 for 30, 60 and 120 min. Quantification of living bacteria was performed by CFU determination and the values are expressed as % survival compared to mock-treated samples. The mean value ± standard deviation is depicted for three independent experiments

Journal: Virulence

Article Title: Respiratory ß-2-Microglobulin exerts pH dependent antimicrobial activity

doi: 10.1080/21505594.2020.1831367

Figure Lengend Snippet: pH-dependent antibacterial activity of purified B2M against L. monocytogenes . A : Amyloidogenic potential of B2M at low pH conditions. The presence of amyloid fibrils was monitored by ThT staining. B2M was either subjected directly to ThT measurement or was incubated at 37°C for 30 min in buffer with the indicated pH. EF-C fibrils served as positive control (pos control). The mean value and standard deviation for two independent experiments is depicted. B : Antibacterial activity of B2M was tested in radial diffusion assays using pH modified agarose solutions (4.5 to 7). Antibacterial activity of B2M in radial diffusion assays could only be observed at pH values lower than 6. C : The pH-dependent effect of B2M (1 mg/ml) against L. monocytogenes in a survival assay. Peptide and mock-treated bacteria were incubated at pH values 7, 5.5 and 4.5 for 30, 60 and 120 min. Quantification of living bacteria was performed by CFU determination and the values are expressed as % survival compared to mock-treated samples. The mean value ± standard deviation is depicted for three independent experiments

Article Snippet: 90 μl of the bacterial suspension was mixed with 10 μl of the desired concentration of B2M (Lee BioSolutions, St. Louis, Missouri, 126–12-10) or with 10 μl of ddH 2 O (negative control) followed by incubation at 37°C.

Techniques: Activity Assay, Purification, Staining, Incubation, Positive Control, Control, Standard Deviation, Diffusion-based Assay, Modification, Clonogenic Cell Survival Assay, Bacteria

Radial diffusion assay of  B2M  fibril formulations.  B2M  (1 mg/ml) was incubated for 30 min at 37°C in 150 µl of assay buffer of pH 4.5 or pH 7 allowing for fibril formation. After centrifugation, the supernatant was collected and the resulting fibril pellet was dissolved in 150 µl of assay buffer of pH 4.5 or pH 7. Depicted are the mean ± standard deviation of the zone of inhibition [cm] in a radial diffusion assay against L. monocytogenes.

Journal: Virulence

Article Title: Respiratory ß-2-Microglobulin exerts pH dependent antimicrobial activity

doi: 10.1080/21505594.2020.1831367

Figure Lengend Snippet: Radial diffusion assay of B2M fibril formulations. B2M (1 mg/ml) was incubated for 30 min at 37°C in 150 µl of assay buffer of pH 4.5 or pH 7 allowing for fibril formation. After centrifugation, the supernatant was collected and the resulting fibril pellet was dissolved in 150 µl of assay buffer of pH 4.5 or pH 7. Depicted are the mean ± standard deviation of the zone of inhibition [cm] in a radial diffusion assay against L. monocytogenes.

Article Snippet: 90 μl of the bacterial suspension was mixed with 10 μl of the desired concentration of B2M (Lee BioSolutions, St. Louis, Missouri, 126–12-10) or with 10 μl of ddH 2 O (negative control) followed by incubation at 37°C.

Techniques: Diffusion-based Assay, Incubation, Centrifugation, Standard Deviation, Inhibition

TEM pictures of L. monocytogenes . Bacterial cells were either mock-treated with H 2 O (a) or treated with 1 mg/ml B2M for 15 min (b) followed by fixation. Ultra-thin sections (80 nm) were imaged in a Zeiss TEM 109 or in a Jeol TEM 1400. Scale bars are 5 µm for upper left, 2 µm for upper right, 1 µm for lower left and 500 nm for lower right pictures

Journal: Virulence

Article Title: Respiratory ß-2-Microglobulin exerts pH dependent antimicrobial activity

doi: 10.1080/21505594.2020.1831367

Figure Lengend Snippet: TEM pictures of L. monocytogenes . Bacterial cells were either mock-treated with H 2 O (a) or treated with 1 mg/ml B2M for 15 min (b) followed by fixation. Ultra-thin sections (80 nm) were imaged in a Zeiss TEM 109 or in a Jeol TEM 1400. Scale bars are 5 µm for upper left, 2 µm for upper right, 1 µm for lower left and 500 nm for lower right pictures

Article Snippet: 90 μl of the bacterial suspension was mixed with 10 μl of the desired concentration of B2M (Lee BioSolutions, St. Louis, Missouri, 126–12-10) or with 10 μl of ddH 2 O (negative control) followed by incubation at 37°C.

Techniques:

Overview of B2M derivatives and their AMP activity. A : Sequence of full-length B2M and the truncated peptides experimentally tested for their antimicrobial activity. Peptides marked with a minus (-) showed no activity against P. aeruginosa at a concentration of 1 mg/ml, whereas the fragments located in the C-terminal part of B2M highlighted with a plus (+) were able to inhibit growth of the bacterium in a radial diffusion assay. B : Derivatives of the C-terminal part of B2M encompassing amino acids 101 to 115 and their activity against P. aeruginosa . All active peptides were tested in triplicates. C : Dose-dependent activity of the B2M derivatives tested in a radial diffusion assay. Depicted is the mean ± standard deviation of three independent assays

Journal: Virulence

Article Title: Respiratory ß-2-Microglobulin exerts pH dependent antimicrobial activity

doi: 10.1080/21505594.2020.1831367

Figure Lengend Snippet: Overview of B2M derivatives and their AMP activity. A : Sequence of full-length B2M and the truncated peptides experimentally tested for their antimicrobial activity. Peptides marked with a minus (-) showed no activity against P. aeruginosa at a concentration of 1 mg/ml, whereas the fragments located in the C-terminal part of B2M highlighted with a plus (+) were able to inhibit growth of the bacterium in a radial diffusion assay. B : Derivatives of the C-terminal part of B2M encompassing amino acids 101 to 115 and their activity against P. aeruginosa . All active peptides were tested in triplicates. C : Dose-dependent activity of the B2M derivatives tested in a radial diffusion assay. Depicted is the mean ± standard deviation of three independent assays

Article Snippet: 90 μl of the bacterial suspension was mixed with 10 μl of the desired concentration of B2M (Lee BioSolutions, St. Louis, Missouri, 126–12-10) or with 10 μl of ddH 2 O (negative control) followed by incubation at 37°C.

Techniques: Activity Assay, Sequencing, Concentration Assay, Diffusion-based Assay, Standard Deviation