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Ground steel massive 384 target plate

Manufactured by Bruker
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The Ground Steel massive 384 target plate is a lab equipment product designed to hold and support samples during analysis. It features a sturdy construction with a 384-well grid layout, providing a reliable platform for various analytical techniques.

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Lab products found in correlation

Flexanalysis 3, by Bruker (3 mentions) Ziptip c4 micro columns, by Merck Group (3 mentions) Autoflex 3, by Bruker (3 mentions) Protein 1 standard calibration mixture, by Bruker (2 mentions) Protein calibration standard 1, by Bruker (1 mentions)

Close spelling variants of this product

Ground steel target plate Ground steel target

3 protocols using ground steel massive 384 target plate

1

MALDI-TOF/TOF Mass Spectrometry of Fab

Check if the same lab product or an alternative is used in the 5 most similar protocols
Prior to the measurement, all Fab preparations were desalted using ZipTip® C4 micro-columns (Millipore) (2 μL sample) with 0.5 μL SA buffer (sinapinic acid, 10 mg/ml in [70:30] Acetonitrile:Trifluoroacetic acid 0.1%), and arrayed onto a Ground Steel massive 384 target plate (Bruker Daltonics). Mass determinations were performed in a matrix-assisted laser desorption/ionization (MALDI), tandem time-of-flight (TOF/TOF) spectrometer Autoflex III (Bruker Daltonics). Mass calibration was performed externally with a Protein Calibration Standard 1 mixture (Bruker Daltonics) in the same mass range as the samples. Data acquisition, peak peaking and subsequent spectra analysis were performed using flexAnalysis 3.0 software (Bruker Daltonics).
Rujas E., Insausti S., Leaman D.P., Carravilla P., González-Resines S., Monceaux V., Sánchez-Eugenia R., García-Porras M., Iloro I., Zhang L., Elortza F., Julien J.P., Saéz-Cirión A., Zwick M.B., Eggeling C., Ojida A., Domene C., Caaveiro J.M, & Nieva J.L. (2020). Affinity for the Interface Underpins Potency of Antibodies Operating In Membrane Environments. Cell reports, 32(7), 108037.
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2

MALDI-TOF Analysis of Conjugated Antibodies

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Prior to the measurement, conjugated antibodies were desalted using ZipTip® C4 micro columns (Millipore) (2 μL sample) with 0.5μL SA buffer (sinapinic acid, 10 mg/mL in [70:30] Acetonitrile:Trifluoroacetic acid 0.1%), and spotted onto a Ground Steel massive 384 target plate (Bruker Daltonics). Mass determination was performed by matrix-assisted laser desorption/ionization-time of flight (MALDI-TOF) analysis in an Autoflex III (Bruker Daltonics). Mass calibration was performed externally with a Protein Calibration Standard 1 (Bruker Daltonics) mixture in the same mass range as the samples. Data acquisition, peak peaking and subsequent spectra analysis were performed using flexAnalysis 3.0 software (Bruker Daltonics).
Rujas E., Leaman D.P., Insausti S., Carravilla P., García-Porras M., Largo E., Morillo I., Sánchez-Eugenia R., Zhang L., Cui H., Iloro I., Elortza F., Julien J.P., Eggeling C., Zwick M.B., Caaveiro J.M, & Nieva J.L. (2021). Focal accumulation of aromaticity at the CDRH3 loop mitigates 4E10 polyreactivity without altering its HIV neutralization profile. iScience, 24(9), 102987.
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3

MALDI-TOF/TOF Mass Spectrometry of Fab

Check if the same lab product or an alternative is used in the 5 most similar protocols
Prior to the measurement, all Fab preparations were desalted using ZipTip® C4 micro-columns (Millipore) (2 μL sample) with 0.5 μL SA buffer (sinapinic acid, 10 mg/ml in [70:30] Acetonitrile:Trifluoroacetic acid 0.1%), and arrayed onto a Ground Steel massive 384 target plate (Bruker Daltonics). Mass determinations were performed in a matrix-assisted laser desorption/ionization (MALDI), tandem time-of-flight (TOF/TOF) spectrometer Autoflex III (Bruker Daltonics). Mass calibration was performed externally with a Protein Calibration Standard 1 mixture (Bruker Daltonics) in the same mass range as the samples. Data acquisition, peak peaking and subsequent spectra analysis were performed using flexAnalysis 3.0 software (Bruker Daltonics).
Rujas E., Insausti S., Leaman D.P., Carravilla P., González-Resines S., Monceaux V., Sánchez-Eugenia R., García-Porras M., Iloro I., Zhang L., Elortza F., Julien J.P., Saéz-Cirión A., Zwick M.B., Eggeling C., Ojida A., Domene C., Caaveiro J.M, & Nieva J.L. (2020). Affinity for the Interface Underpins Potency of Antibodies Operating In Membrane Environments. Cell reports, 32(7), 108037.
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