Geno/Grinder® 2010, 115V

Geno/Grinder® 2010 (Open)

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SKU: SP 2010-115

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*Available to U.S. Customers Only

The Geno/Grinder® 2010 is today's most versatile high throughput homogenizer.

Automated mechanical disruption through bead beating, ideal for high-throughput homogenization.
Programmable touch screen control panel for run time, rate, cycles and pause time. Up to 500 protocols can be saved for recall.
Linear shaking of deep-well titer plates, vial sets, and centrifuge tubes in a vertical motion for consistent processing.
Adjustable clamp allows users to secure a full range of sample vials from 2mL (x96), 4mL (x96), 15 mL (x20) to 50mL (x10) self-standing vials, or up to six deep-well titer plates (*optional stacking tray required). Also accommodates conical bottom centrifuge tubes.
Typical sample processing time of 1-2 minutes.
Optional Cryo-Blocks enable cryogenic grinding and preserve temperature sensitive samples for RNA and protein extractions. For more information, see Geno/Grinder 2010 Accessories.
Can be used for a wide variety of sample types, including cell cultures, cannabis, yeast, bacteria, fungi, animal tissue, plants, seeds, biofuels, etc.

Specifications

Clamp Movement	1.25in (3.2cm) vertical
Clamp Speed	Adjustable from 500-1750 strokes/minute
Timer	Digital display in Minutes:Seconds (max 20:00)
USB port	Run history is recorded and can be exported
Voltage	115V/60Hz
CE Approved	Yes
Dimensions	14.00 in (35.6 cm) wide x 22.5 in. (57.2 cm) deep x 28 in. (71.1 cm) high
Net Weight	106 lbs (48 kg)
Motor	1/3 hp
Power Cord	3-prong grounded plug, 115V / 60Hz

Unsure of which pre-filled tubes to use with your samples? See our comparison of pre-filled disruption tubes.

Citations

Campbell, J. (2021). Characterization of large muscadine (Muscadinia rotundifolia Michx) population for diverse phenological and reproductive performance traits. https://www.proquest.com/dissertations-theses/characterization-large-muscadine-em-muscadinia/docview/2827405157/se-2 (The study examines muscadine grape traits like flowering, ripening, fruit set, and yield to aid breeding and genetic research)

de Kerdrel, G. A., Andersen, J. C., Kennedy, S. R., Gillespie, R., Krehenwinkel, H. (2020) Rapid and cost-effective generation of single specimen multilocus barcoding data from whole arthropod communities by multiple levels of multiplexing. Scientific Reports, 10 (1), 1–12. https://doi.org/10.1038/s41598-019-54927-z. (This study introduces a cost-effective sequencing method to generate barcode data for thousands of arthropods, demonstrated with Hawaiian biodiversity assessments)

Laraba, I., McCormick, S. P., Vaughan, M. M., Geiser, D. M., & O’Donnell, K. (2021). Phylogenetic diversity, trichothecene potential, and pathogenicity within Fusarium sambucinum species complex. PLoS ONE, 16(1), e0245037. https://doi.org/10.1371/journal.pone.0245037 (The Fusarium sambucinum species complex includes 74 species producing diverse trichothecenes, with aggressive strains causing wheat disease and synthesizing novel toxins)

Li, M. (2020). Transcriptional regulation of PR5 and roles of a PR5-derived peptide in plant immunity. https://www.proquest.com/dissertations-theses/transcriptional-regulation-pr5-roles-derived/docview/2430165707/se-2. (In Arabidopsis, NPR1 and TCP factors regulate PR5, while PR5_1 peptide boosts immunity via HHP2)

Petrella, D. P., & Watkins, E. (2020). Variation in fine fescue taxa response to simulated foliar shade. Crop Science, 60(6), 3377–3394. https://doi.org/10.1002/csc2.20279 (Chewings fescue shows the best shade tolerance among fine fescues, with potential for improvement through breeding)

Shaddox, T. W., Unruh, J. B., & Restuccia, N. G. (2020). St. Augustinegrass quality and nutrient content in response to granular and foliar iron, manganese, and magnesium. Crop Science, 60(6), 3314–3327. https://doi.org/10.1002/csc2.20244 (Foliar iron improved St. Augustinegrass quality, while granular iron, manganese, and magnesium had little to no impact)

*Available to U.S. Customers Only

The Geno/Grinder® 2010

is the most versatile high throughput homogenizer available today.

Automated mechanical disruption through bead beating, ideal for high-throughput homogenization.
Programmable touch screen control panel for run time, rate, cycles and pause time. Up to 500 protocols can be saved for recall.
Linear shaking of deep-well titer plates, vial sets, and centrifuge tubes in a vertical motion for consistent processing.
Adjustable clamp allows users to secure a full range of sample vials from 2mL (x96), 4mL (x96), 15 mL (x20) to 50mL (x10) self-standing vials, or up to six deep-well titer plates (*optional stacking tray required). Also accommodates conical bottom centrifuge tubes.
Typical sample processing time of 1-2 minutes.
Optional Cryo-Blocks enable cryogenic grinding and preserve temperature sensitive samples for RNA and protein extractions. For more information, see Geno/Grinder 2010 Accessories.
Can be used for a wide variety of sample types, including cell cultures, cannabis, yeast, bacteria, fungi, animal tissue, plants, seeds, biofuels, etc.

Specifications

Specifications
Clamp Movement	1.25in (3.2cm) vertical
Clamp Speed	Adjustable from 500-1750 strokes/minute
Timer	Digital display in Minutes:Seconds (max 20:00)
USB port	Run history is recorded and can be exported
Voltage	115V/60Hz
CE Approved	Yes
Dimensions	14.00 in (35.6 cm) wide x 22.5 in. (57.2 cm) deep x 28 in. (71.1 cm) high
Net Weight	106 lbs (48 kg)
Motor	1/3 hp
Power Cord	3-prong grounded plug, 115V / 60Hz

Unsure of which pre-filled tubes to use with your samples? Follow the link to see our comparison of pre-filled disruption tubes.

Citations

Leopold, D. R.; Busby, P. E. Joint Effects of Host Genotype and Species Arrival Order Govern Microbiome Composition and Function. bioRxiv 2020, 2020.02.28.970582. https://doi.org/10.1101/2020.02.28.970582.

de Kerdrel, G. A.; Andersen, J. C.; Kennedy, S. R.; Gillespie, R.; Krehenwinkel, H. Rapid and Cost-Effective Generation of Single Specimen Multilocus Barcoding Data from Whole Arthropod Communities by Multiple Levels of Multiplexing. Scientific Reports 2020, 10 (1), 1–12. https://doi.org/10.1038/s41598-019-54927-z.

Roth, M. G.; Oudman, K. A.; Griffin, A.; Jacobs, J. L.; Sang, H.; Chilvers, M. I. Diagnostic QPCR Assay to Detect Fusarium Brasiliense, a Causal Agent of Soybean Sudden Death Syndrome and Root Rot of Dry Bean. Plant Disease 2019, 104 (1), 246–254. https://doi.org/10.1094/PDIS-01-19-0016-RE.

Laraba, I.; Keddad, A.; Boureghda, H.; Abdallah, N.; Vaughan, M. M.; Proctor, R. H.; Busman, M.; O’Donnell, K. Fusarium Algeriense, Sp. Nov., a Novel Toxigenic Crown Rot Pathogen of Durum Wheat from Algeria Is Nested in the Fusarium Burgessii Species Complex. Mycologia 2017, 109 (6), 935–950. https://doi.org/10.1080/00275514.2018.1425067.

Krehenwinkel, H.; Wolf, M.; Lim, J. Y.; Rominger, A. J.; Simison, W. B.; Gillespie, R. G. Estimating and Mitigating Amplification Bias in Qualitative and Quantitative Arthropod Metabarcoding. Scientific Reports 2017, 7 (1), 17668. https://doi.org/10.1038/s41598-017-17333-x.

Hung, C.-S.; Li, H.-Y.; Kuo, C.-H.; Lin, M.-S.; Kuo, T.-C.; Tsai, S.-J.; Liu, P.-H.; Lin, C.-H.; Yang, C.-Y.; Chuang, L.-M.; et al. Fasting but Not Changes of Plasma Metabolome during Oral Glucose Tolerance Tests Improves the Diagnosis of Severe Coronary Arterial Stenosis. Clinical Endocrinology 2015, 83 (4), 483–489. https://doi.org/10.1111/cen.12713.

Wu, C. A.; Murray, L. A.; Heffernan, K. E. Evidence for Natural Hybridization between Native and Introduced Lineages of Phragmites Australis in the Chesapeake Bay Watershed. American Journal of Botany 2015, 102 (5), 805–812. https://doi.org/10.3732/ajb.1500018.

Khadilkar, A. S.; Yadav, U. P.; Salazar, C.; Shulaev, V.; Paez-Valencia, J.; Pizzio, G. A.; Gaxiola, R. A.; Ayre, B. G. Constitutive and Companion Cell-Specific Overexpression of AVP1, Encoding a Proton-Pumping Pyrophosphatase, Enhances Biomass Accumulation, Phloem Loading, and Long-Distance Transport. Plant Physiology 2016, 170 (1), 401–414. https://doi.org/10.1104/pp.15.01409.