To quickly compare features and select the Greiner CrystalQuick plate that best fits your needs please refer to the Greiner CrystalQuick Plate Summary pdf on this page.

CrystalQuick™ 96 Well, Greiner 609120

CrystalQuick™ 96 Well, Greiner 609120

1. Semi-automatic protein crystallization system that allows in situ observation of X-ray diffraction from crystals in the drop. N. Watanabe, H. Murai and I. Tanaka. Acta Cryst. (2002). D58, 1527-1530.

2. Practical implementations for improving the throughput in a manual crystallization setup. Jérôme Basquin , Christian Biertümpfel and Dietrich Suck. Journal of Applied Crystallography Volume 38 Page 568 – June 2005.

3. Crystallization and preliminary crystallographic analysis of human common-type acylphosphatase. Rachel C. Y. Yeung , Sonia Y. Lam and Kam-Bo Wong. Acta Crystallographica Section F, Volume 62 Page 80 – January 2006.

Hampton Research, first in crystallization since 1991, developing and delivering crystallization and optimization screens, reagents, plates, and other tools for the crystallization of biological macromolecules, including proteins (antibody), peptides (insulin), and nucleic acids (DNA).

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To quickly compare features and select the Greiner CrystalQuick plate that best fits your needs please refer to the Greiner CrystalQuick Plate Summary pdf on this page.

CrystalQuick™ Plus 96 Well, Greiner 609130

CrystalQuick™ Plus 96 Well, Greiner 609130

1. Semi-automatic protein crystallization system that allows in situ observation of X-ray diffraction from crystals in the drop. N. Watanabe, H. Murai and I. Tanaka. Acta Cryst. (2002). D58, 1527-1530.

2. Practical implementations for improving the throughput in a manual crystallization setup. Jérôme Basquin , Christian Biertümpfel and Dietrich Suck. Journal of Applied Crystallography Volume 38 Page 568 – June 2005.

3. Crystallization and preliminary crystallographic analysis of human common-type acylphosphatase. Rachel C. Y. Yeung , Sonia Y. Lam and Kam-Bo Wong. Acta Crystallographica Section F, Volume 62 Page 80 – January 2006.

Hampton Research, first in crystallization since 1991, developing and delivering crystallization and optimization screens, reagents, plates, and other tools for the crystallization of biological macromolecules, including proteins (antibody), peptides (insulin), and nucleic acids (DNA).

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To quickly compare features and select the Greiner CrystalQuick plate that best fits your needs please refer to the Greiner CrystalQuick Plate Summary pdf on this page.

CrystalQuick™ 96 Well, Greiner 609171

CrystalQuick™ 96 Well, Greiner 609171

1. Semi-automatic protein crystallization system that allows in situ observation of X-ray diffraction from crystals in the drop. N. Watanabe, H. Murai and I. Tanaka. Acta Cryst. (2002). D58, 1527-1530.

2. Practical implementations for improving the throughput in a manual crystallization setup. Jérôme Basquin , Christian Biertümpfel and Dietrich Suck. Journal of Applied Crystallography Volume 38 Page 568 – June 2005.

3. Crystallization and preliminary crystallographic analysis of human common-type acylphosphatase. Rachel C. Y. Yeung , Sonia Y. Lam and Kam-Bo Wong. Acta Crystallographica Section F, Volume 62 Page 80 – January 2006.

Hampton Research, first in crystallization since 1991, developing and delivering crystallization and optimization screens, reagents, plates, and other tools for the crystallization of biological macromolecules, including proteins (antibody), peptides (insulin), and nucleic acids (DNA).

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To quickly compare features and select the Greiner CrystalQuick plate that best fits your needs please refer to the Greiner CrystalQuick Plate Summary pdf on this page.

CrystalQuick™ Plus 96 Well, Greiner 609180

CrystalQuick™ Plus 96 Well, Greiner 609180

1. Semi-automatic protein crystallization system that allows in situ observation of X-ray diffraction from crystals in the drop. N. Watanabe, H. Murai and I. Tanaka. Acta Cryst. (2002). D58, 1527-1530.

2. Practical implementations for improving the throughput in a manual crystallization setup. Jérôme Basquin , Christian Biertümpfel and Dietrich Suck. Journal of Applied Crystallography Volume 38 Page 568 – June 2005.

3. Crystallization and preliminary crystallographic analysis of human common-type acylphosphatase. Rachel C. Y. Yeung , Sonia Y. Lam and Kam-Bo Wong. Acta Crystallographica Section F, Volume 62 Page 80 – January 2006.

Hampton Research, first in crystallization since 1991, developing and delivering crystallization and optimization screens, reagents, plates, and other tools for the crystallization of biological macromolecules, including proteins (antibody), peptides (insulin), and nucleic acids (DNA).

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To quickly compare features and select the Greiner CrystalQuick plate that best fits your needs please refer to the Greiner CrystalQuick Plate Summary pdf on this page.

CrystalQuick™ 96 Well, Greiner 609801

CrystalQuick™ 96 Well, Greiner 609801

1. Semi-automatic protein crystallization system that allows in situ observation of X-ray diffraction from crystals in the drop. N. Watanabe, H. Murai and I. Tanaka. Acta Cryst. (2002). D58, 1527-1530.

2. Practical implementations for improving the throughput in a manual crystallization setup. Jérôme Basquin , Christian Biertümpfel and Dietrich Suck. Journal of Applied Crystallography Volume 38 Page 568 – June 2005.

3. Crystallization and preliminary crystallographic analysis of human common-type acylphosphatase. Rachel C. Y. Yeung , Sonia Y. Lam and Kam-Bo Wong. Acta Crystallographica Section F, Volume 62 Page 80 – January 2006.

Hampton Research, first in crystallization since 1991, developing and delivering crystallization and optimization screens, reagents, plates, and other tools for the crystallization of biological macromolecules, including proteins (antibody), peptides (insulin), and nucleic acids (DNA).

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To quickly compare features and select the Greiner CrystalQuick plate that best fits your needs please refer to the Greiner CrystalQuick Plate Summary pdf on this page.

CrystalQuick™ 96 Well, Greiner 609820

CrystalQuick™ 96 Well, Greiner 609820

1. Semi-automatic protein crystallization system that allows in situ observation of X-ray diffraction from crystals in the drop. N. Watanabe, H. Murai and I. Tanaka. Acta Cryst. (2002). D58, 1527-1530.

2. Practical implementations for improving the throughput in a manual crystallization setup. Jérôme Basquin , Christian Biertümpfel and Dietrich Suck. Journal of Applied Crystallography Volume 38 Page 568 – June 2005.

3. Crystallization and preliminary crystallographic analysis of human common-type acylphosphatase. Rachel C. Y. Yeung , Sonia Y. Lam and Kam-Bo Wong. Acta Crystallographica Section F, Volume 62 Page 80 – January 2006.

Hampton Research, first in crystallization since 1991, developing and delivering crystallization and optimization screens, reagents, plates, and other tools for the crystallization of biological macromolecules, including proteins (antibody), peptides (insulin), and nucleic acids (DNA).

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To quickly compare features and select the Greiner CrystalQuick plate that best fits your needs please refer to the Greiner CrystalQuick Plate Summary pdf on this page.

CrystalQuick™ Plus 96 Well, Greiner 609830

CrystalQuick™ Plus 96 Well, Greiner 609830

1. Semi-automatic protein crystallization system that allows in situ observation of X-ray diffraction from crystals in the drop. N. Watanabe, H. Murai and I. Tanaka. Acta Cryst. (2002). D58, 1527-1530.

2. Practical implementations for improving the throughput in a manual crystallization setup. Jérôme Basquin , Christian Biertümpfel and Dietrich Suck. Journal of Applied Crystallography Volume 38 Page 568 – June 2005.

3. Crystallization and preliminary crystallographic analysis of human common-type acylphosphatase. Rachel C. Y. Yeung , Sonia Y. Lam and Kam-Bo Wong. Acta Crystallographica Section F, Volume 62 Page 80 – January 2006.

Hampton Research, first in crystallization since 1991, developing and delivering crystallization and optimization screens, reagents, plates, and other tools for the crystallization of biological macromolecules, including proteins (antibody), peptides (insulin), and nucleic acids (DNA).

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To quickly compare features and select the Greiner CrystalQuick plate that best fits your needs please refer to the Greiner CrystalQuick Plate Summary pdf on this page.

CrystalQuick™ 96 Well, Greiner 609871

CrystalQuick™ 96 Well, Greiner 609871

1. Semi-automatic protein crystallization system that allows in situ observation of X-ray diffraction from crystals in the drop. N. Watanabe, H. Murai and I. Tanaka. Acta Cryst. (2002). D58, 1527-1530.

2. Practical implementations for improving the throughput in a manual crystallization setup. Jérôme Basquin , Christian Biertümpfel and Dietrich Suck. Journal of Applied Crystallography Volume 38 Page 568 – June 2005.

3. Crystallization and preliminary crystallographic analysis of human common-type acylphosphatase. Rachel C. Y. Yeung , Sonia Y. Lam and Kam-Bo Wong. Acta Crystallographica Section F, Volume 62 Page 80 – January 2006.

Hampton Research, first in crystallization since 1991, developing and delivering crystallization and optimization screens, reagents, plates, and other tools for the crystallization of biological macromolecules, including proteins (antibody), peptides (insulin), and nucleic acids (DNA).

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Plate Dimensions: 127.76 mm x 85.48 mm x 8.0 mm.
Conical well with 19 µl drop volume.
Flat bottom well diameter: 2 mm.

96 Well Imp@ct Plate, Greiner 673101

96 Well Imp@ct Plate, Greiner 673101

Hampton Research, first in crystallization since 1991, developing and delivering crystallization and optimization screens, reagents, plates, and other tools for the crystallization of biological macromolecules, including proteins (antibody), peptides (insulin), and nucleic acids (DNA).

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Greased CrystalDrop™ Lid, Greiner 609050

1. Semi-automatic protein crystallization system that allows in situ observation of X-ray diffraction from crystals in the drop. N. Watanabe, H. Murai and I. Tanaka. Acta Cryst. (2002). D58, 1527-1530.

2. Practical implementations for improving the throughput in a manual crystallization setup. Jérôme Basquin , Christian Biertümpfel and Dietrich Suck. Journal of Applied Crystallography Volume 38 Page 568 – June 2005.

3. Crystallization and preliminary crystallographic analysis of human common-type acylphosphatase. Rachel C. Y. Yeung , Sonia Y. Lam and Kam-Bo Wong. Acta Crystallographica Section F, Volume 62 Page 80 – January 2006.

Hampton Research, first in crystallization since 1991, developing and delivering crystallization and optimization screens, reagents, plates, and other tools for the crystallization of biological macromolecules, including proteins (antibody), peptides (insulin), and nucleic acids (DNA).

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CrystalDrop™ Lid, Greiner 609150

CrystalDrop™ Lid, Greiner 609150

1. Semi-automatic protein crystallization system that allows in situ observation of X-ray diffraction from crystals in the drop. N. Watanabe, H. Murai and I. Tanaka. Acta Cryst. (2002). D58, 1527-1530.

2. Practical implementations for improving the throughput in a manual crystallization setup. Jérôme Basquin , Christian Biertümpfel and Dietrich Suck. Journal of Applied Crystallography Volume 38 Page 568 – June 2005.

3. Crystallization and preliminary crystallographic analysis of human common-type acylphosphatase. Rachel C. Y. Yeung , Sonia Y. Lam and Kam-Bo Wong. Acta Crystallographica Section F, Volume 62 Page 80 – January 2006.

Hampton Research, first in crystallization since 1991, developing and delivering crystallization and optimization screens, reagents, plates, and other tools for the crystallization of biological macromolecules, including proteins (antibody), peptides (insulin), and nucleic acids (DNA).

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The Microplate Lid is a temporary cover for the crystallization screens in 96 deep well format. The single position, high profile cover with individual condensation rings over each reagent well can help minimize reagent evaporation from 96 deep well reagent plates as well as protect the reagents from particulate and contamination. The individually wrapped, sterile Microplate Lid is made from optically clear polystyrene. Greiner 656171.

The Cap Mat is made of ethyl vinyl acetate (EVA). Resistant to DMSO and can be used in a temperature range between -20 and +60 degrees Celsius. Suitable for sealing Greiner 780261 1 milliliter Deep Well Plate (HR3-105). These cap mats are not piercable. Supplied sterile. Greiner part number 381061.

MASTERBLOCK® 96 Deep Well polypropylene plate

Microplate Lid

Cap Mat for MASTERBLOCK®

Hampton Research, first in crystallization since 1991, developing and delivering crystallization and optimization screens, reagents, plates, and other tools for the crystallization of biological macromolecules, including proteins (antibody), peptides (insulin), and nucleic acids (DNA).

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The plates can be sealed using Crystal Clear Sealing Film (HR3-609), 3 inch wide Crystal Clear Sealing Tape (HR4-506) or ClearSeal Film™ (HR4-521). Corning has discontinued 3557 – special pricing and limited inventory available for this item only.

Corning 3550

Corning 3550

Hampton Research, first in crystallization since 1991, developing and delivering crystallization and optimization screens, reagents, plates, and other tools for the crystallization of biological macromolecules, including proteins (antibody), peptides (insulin), and nucleic acids (DNA).

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The plates can be sealed using Crystal Clear Sealing Film (HR3-609), 3 inch wide Crystal Clear Sealing Tape (HR4-506) or ClearSeal Film™ (HR4-521). Corning has discontinued 3557 – special pricing and limited inventory available for this item only.

Corning 3552

Corning 3552

Hampton Research, first in crystallization since 1991, developing and delivering crystallization and optimization screens, reagents, plates, and other tools for the crystallization of biological macromolecules, including proteins (antibody), peptides (insulin), and nucleic acids (DNA).

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The plates can be sealed using Crystal Clear Sealing Film (HR3-609), 3 inch wide Crystal Clear Sealing Tape (HR4-506) or ClearSeal Film™ (HR4-521). Corning has discontinued 3557 – special pricing and limited inventory available for this item only.

Corning 3553

Corning 3553

Hampton Research, first in crystallization since 1991, developing and delivering crystallization and optimization screens, reagents, plates, and other tools for the crystallization of biological macromolecules, including proteins (antibody), peptides (insulin), and nucleic acids (DNA).

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The plates can be sealed using Crystal Clear Sealing Film (HR3-609), 3 inch wide Crystal Clear Sealing Tape (HR4-506) or ClearSeal Film™ (HR4-521). Corning has discontinued 3557 – special pricing and limited inventory available for this item only.

Corning 3556

Corning 3556

Hampton Research, first in crystallization since 1991, developing and delivering crystallization and optimization screens, reagents, plates, and other tools for the crystallization of biological macromolecules, including proteins (antibody), peptides (insulin), and nucleic acids (DNA).

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The plates can be sealed using Crystal Clear Sealing Film (HR3-609), 3 inch wide Crystal Clear Sealing Tape (HR4-506) or ClearSeal Film™ (HR4-521). Corning has discontinued 3557 – special pricing and limited inventory available for this item only.

Corning 3557

Hampton Research, first in crystallization since 1991, developing and delivering crystallization and optimization screens, reagents, plates, and other tools for the crystallization of biological macromolecules, including proteins (antibody), peptides (insulin), and nucleic acids (DNA).

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The well surfaces are treated to be hydrophilic for improved drop mixing. Both versions are compatible with 8 and 12 channel manual pipetters, automated liquid handling work stations, and imaging systems. Both versions are manufactured from an advanced polymer with high resistance to commonly used protein crystallization reagents. The advanced polymer material provides for low-background polarization and high optical clarity so protein crystals may be viewed under polarized light with minimal background interference. Low water absorption of the polymer prevents loss of protein drop volume.

The plates can be sealed using Crystal Clear Sealing Film (HR3-609), 3 inch wide Crystal Clear Sealing Tape (HR4-506) or ClearSeal Film™ (HR4-521)

CrystalEX 96 Well, Conical Bottom, Corning 3773

CrystalEX 96 Well, Conical Bottom, Corning 3773

Hampton Research, first in crystallization since 1991, developing and delivering crystallization and optimization screens, reagents, plates, and other tools for the crystallization of biological macromolecules, including proteins (antibody), peptides (insulin), and nucleic acids (DNA).

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The well surfaces are treated to be hydrophilic for improved drop mixing. Both versions are compatible with 8 and 12 channel manual pipetters, automated liquid handling work stations, and imaging systems. Both versions are manufactured from an advanced polymer with high resistance to commonly used protein crystallization reagents. The advanced polymer material provides for low-background polarization and high optical clarity so protein crystals may be viewed under polarized light with minimal background interference. Low water absorption of the polymer prevents loss of protein drop volume.

The plates can be sealed using Crystal Clear Sealing Film (HR3-609), 3 inch wide Crystal Clear Sealing Tape (HR4-506) or ClearSeal Film™ (HR4-521)

CrystalEX 96 Well, Flat Bottom, Corning 3785

CrystalEX 96 Well, Flat Bottom, Corning 3785

Hampton Research, first in crystallization since 1991, developing and delivering crystallization and optimization screens, reagents, plates, and other tools for the crystallization of biological macromolecules, including proteins (antibody), peptides (insulin), and nucleic acids (DNA).

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These reagents can perturb and manipulate sample-sample and sample-solvent interactions, as well as perturb water structure which can alter and improve both the solubility and crystallization of a sample. Additives can stabilize or engender conformity by specific interaction with the macromolecules. There are numerous reports of the use of additives to improve the quality and size of macromolecular crystals.^1-5

Additive screen reagent classifications include multivalent, salt, amino acid, dissociating agent, linker, polyamine, osmolyte, chaotrope, co-factor, reducing agent, chelating agent, polymer, carbohydrate, non-detergent, amphiphile, detergent, non-volatile organic and volatile organic.

Additive Screen contains 96 unique reagents, 1 ml each.

Additive Screen HT contains 96 unique reagents, 1 ml each, in a single Deep Well block.

Additive Screen

Additive Screen HT

1. Crystallization of membrane proteins., Edited by Hartmut Michel, CRC Press (1991).

2. Crystallization of Nucleic Acids and Proteins: A Practical Approach., Edited by A. Ducruix and R. Giege, Oxford University Press (1992).

3. Cudney, R., et al., Screening and optimization strategies for macromolecular crystal growth., Acta Cryst. (1994) D50, 414-423.

4. Sousa R., Use of glycerol, polyols and other protein structure stabilizing agents in protein crystallization., Acta Cryst. (1995) D51, 271-277.

5. Trakhanov, S. and Quiocho, F.A., Influence of divalent cations on protein crystallization., Protein Science (1995) 4, 9, 1914-1919.

6. Crystallization and preliminary X-ray diffraction analysis of YhbJ from Escherichia coli, a key protein involved in the GlmYZ sRNA regulatory cascade. M. Resch, Y. Gopel, B. Gorke and R. Ficner. M. Resch, Y. Gopel, B. Gorke and R. Ficner.

7. Crystal-contact engineering to obtain a crystal form of the Kelch domain of human Keap1 suitable for ligand-soaking experiments. Stefan Horer, Dirk Reinert, Katja Ostmann, Yvette Hoevels and Herbert Nar. Acta Cryst. (2013). F69, 592-596.

8. Thermofluor-based optimization strategy for the stabilization and crystallization of Campylobacter jejuni desulforubrerythrin. Santos SP, Bandeiras TM, Pinto AF, Teixeira M, Carrondo MA, Romão CV. Protein Expr Purif. 2012 Feb;81(2):193-200. doi: 10.1016/j.pep.2011.10.001. Epub 2011 Oct 24. (Thermofluor using the Additive Screen)

Hampton Research, first in crystallization since 1991, developing and delivering crystallization and optimization screens, reagents, plates, and other tools for the crystallization of biological macromolecules, including proteins (antibody), peptides (insulin), and nucleic acids (DNA).

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