GRAS Screen™ 1 • GRAS Screen™ 2蛋白结晶试剂盒Hampton Research

Hampton Research蛋白结晶试剂盒

GRAS Screen™ 1 • GRAS Screen™ 2
GRAS Screen™ 1 • GRAS Screen™ 2

GRAS Screen™ 1 • GRAS Screen™ 2

GRAS Screen™ 1 • GRAS Screen™ 2

GRAS Screen™ 1 • GRAS Screen™ 2

GRAS Screen™ 1 • GRAS Screen™ 2

Products > Crystallization Screens > GRAS Screens > GRAS Screen™ 1 • GRAS Screen™ 2

GRAS Screen™ 1 • GRAS Screen™ 2

Applications

  • GRAS reagent crystallization screen for proteins, including monoclonal antibodies, where Polyethylene glycol is the primary, and Salt the secondary reagent, sampling pH 4-9
  • Identify GRAS based reagents that promote crystallization of biotherapeutics for bioprocess, bioformulation, and continuous flow manufacturing applications

Features

  • Developed at Hampton Research
  • Generally Recognized As Safe reagent formulation
  • Samples pH 4.0 – 9.0 without an added buffer
  • Primary crystallization reagent:
    • GRAS Screen 1: PEG 300, 400, MME 550, & 600
    • GRAS Screen 2: PEG 1,000, MME 2,000, 3,350, & 4,000
  • Secondary crystallization reagent:
    • 24 unique salts
  • Compatible with Vapor diffusion, microbatch, free interface diffusion
  • Reagents soluble between 4°C and 30°C
  • Antibody crystallization screen
  • Membrane protein crystallization screen
    • LCP compatible

Description

GRAS Screen™ 1 and GRAS Screen™ 2 were developed by Hampton Research for the crystallization of proteins, including monoclonal antibodies.

Each of the chemicals in GRAS Screen 1 and 2 have been used under one or more of the following categories. As (1) a Generally Recognized As Safe (GRAS) substance, (2) a pharmaceutical excipient, (3) a normal physiological constituent, (4) a metabolic byproduct, and/or (5) a Everything Added to Food in the United States (EAFUS) substance.

GRAS Screen 1 samples four low molecular weight Polyethylene glycols (300, 400, MME 550, and 600) versus twenty-four salts, encompassing pH 4-9. GRAS Screen 1 is supplied in a 96 Deep Well block format and is compatible with robotic and multi-channel pipet liquid handling systems. GRAS Screen 1 is compatible with vapor diffusion, free interface diffusion, and microbatch crystallization methods. For research use only.

GRAS Screen 2 samples four medium molecular weight Polyethylene glycols (1,000, MME 2,000, 3,350, & 4,000) versus twenty-four salts, encompassing pH 4-9. GRAS Screen 2 is supplied in a 96 Deep Well block format and is compatible with robotic and multi-channel pipet liquid handling systems. GRAS Screen 2 is compatible with vapor diffusion, free interface diffusion, and microbatch crystallization methods. For research use only.

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GRAS Screen™ 1 • GRAS Screen™ 2

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GRAS Screen™ 1 • GRAS Screen™ 2
GRAS Screen™ 1 • GRAS Screen™ 2
GRAS Screen™ 1 • GRAS Screen™ 2
GRAS Screen™ 1 • GRAS Screen™ 2
GRAS Screen™ 1 • GRAS Screen™ 2

GRAS Screen™ 1 • GRAS Screen™ 2

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GRAS Screen™ 1 • GRAS Screen™ 2
GRAS Screen™ 1 • GRAS Screen™ 2
GRAS Screen™ 1 • GRAS Screen™ 2
GRAS Screen™ 1 • GRAS Screen™ 2
GRAS Screen™ 1 • GRAS Screen™ 2

CAT NO

HR2-451

NAME

GRAS Screen 1

DESCRIPTION

1 ml, Deep Well block format

PRICE

$161.00

cart quote

CAT NO

HR2-452

NAME

GRAS Screen 2

DESCRIPTION

1 ml, Deep Well block format

PRICE

$161.00

cart quote

Support Material(s)

GRAS Screen™ 1 • GRAS Screen™ 2 HR2-451 GRAS Screen 1 DocumentsGRAS Screen™ 1 • GRAS Screen™ 2 HR2-451 GRAS Screen 1 SDSGRAS Screen™ 1 • GRAS Screen™ 2 HR2-452 GRAS Screen 2 DocumentsGRAS Screen™ 1 • GRAS Screen™ 2 HR2-452 GRAS Screen 2 SDSGRAS Screen™ 1 • GRAS Screen™ 2 GRAS Screen 1 & GRAS Screen 2 Formulation & Scoring Data

Related Item(S)

  • Individual GRAS Screen 1 Reagents
  • Individual GRAS Screen 2 Reagents

References

1. Optimization of crystallization conditions for biological macromolecules. Alexander McPherson and Bob Cudney. Acta Crystallographica Section F Volume 70, Issue 11, pages 1445-1467, November 2014.

2. Crystallization of intact monoclonal antibodies. Harris LJ, Skaletsky E, McPherson A. Proteins. 1995 Oct;23(2):285-9.

3. Crystalline monoclonal antibodies for subcutaneous delivery. Yang MX1, Shenoy B, Disttler M, Patel R, McGrath M, Pechenov S, Margolin AL. Proc Natl Acad Sci U S A. 2003 Jun 10;100(12):6934-9.

4. Fast and Scalable Purification of a Therapeutic Full-Length Antibody Based on Process Crystallization. Dariusch Hekmat et al, Biotechnology and Bioengineering, Vol. 110, No. 9, September, 2013.

5. Towards Protein Crystallization as a Process Step in Downstream Processing of Therapeutic Antibodies: Screening and Optimization at Microbatch Scale. Yuguo Zang et al, PLoS One. 2011; 6(9): e25282.

6. Crystallization as a tool for bioseparation. Bob Cudney, Am Biotechnol Lab. 1994 Jun;12(7):42.

7. Large-scale crystallization of proteins for purification and formulation. Hekmat D. Bioprocess Biosyst Eng. 2015 Jul;38(7):1209-31. doi: 10.1007/s00449-015-1374-y

8. Using X-Ray Crystallography to Simplify and Accelerate Biologics Drug Development. Brader ML, Baker EN, Dunn MF, Laue TM, Carpenter JF. J Pharm Sci. 2017 Feb;106(2):477-494. doi: 10.1016/j.xphs.2016.10.017.

9. Excipients and Their Role in Approved Injectable Products: Current Usage and Future Directions. Sandeep Nema and Ronald J. Brendell, PDA J Pharm Sci and Tech 2011, 65 287-332.

GRAS Screen™ 1 • GRAS Screen™ 2 GRAS Screen™ 1 • GRAS Screen™ 2

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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