Anti-Phytochelatin Synthase [mAbPS2, 2.8H4.A7.C1] Antibody

This mouse IgG2a monoclonal antibody was generated against synthetic peptide and recognizes plants and fission yeast (Schizosaccharomyces pombe) phytochelatin synthetase (PS), N-MAP.

Highlights:

  • Recognizes plants and fission yeast (Schizosaccharomyces pombe) phytochelatin synthetase (PS), N-MAP SEQ: NIVKRAVPELLRGMTMATPNIGLIKNKVV
  • Useful for the study of synthesis of, and development of, phytochelatins and related metabolic pathways, as well as in the development of phytoremediation tools, and in the study of metal toxicity in plants and closely related organisms
  • Suitable for Immunohistochemistry, ELISA and Western Blot applications

Together with gamma –glutamyl Cys sythetase (γ-ECS) and glutathione synthetase, phytochelatin synthetase (PS), is an enzyme involved in, and required for, synthetizing phytochelatins (PC). In certain plants, deficiency of such enzymes leads to low tolerance to metal contamination while mutants over-expressing them are highly tolerant to metal contamination and may be used in phyto-remediation of heavy metals. Monoclonal antibodies to PC were developed using N-terminal peptides synthesized as MAPs. N-terminal MAP was 29 amino acids long. They are useful for the study of synthesis and development of phytochelatins and related metabolic pathways, as well as in the development of phtoremediation tools and in the study of metal toxicity in plants and closely related organisms.

From the laboratory of Richard B. Meagher, PhD, University of Georgia.

Catalog Number Product DataSheet Size AVAILABILITY Price Qty
EGA099
Anti-Phytochelatin Synthase [mAbPS2, 2.8H4.A7.C1] Antibody
100ug 4-6 weeks
Regular Price:$355.00
On Sale:
Specifications

Product Type: Antibody
Antigen: Phytochelatin synthetase (PS), N-MAP
Accession ID: Q9S7Z3
Molecular Weight: 57 kDa
Isotype: IgG2a
Clonality: Monoclonal
Clone Name: mAbPS2 (2.8H4.A7.C1)
Reactivity: Plants and fission yeast (Schizosaccharomyces pombe)
Immunogen: Synthetic Peptide
Species Immunized: Mouse
Purification Method: Protein G
Buffer: PBS, 0.05% (w/v) Sodium Azide
Tested Applications: WB, ELISA, IF
Storage: -20C
Shipped: Cold Packs

Provider
From the laboratory of Richard B. Meagher, PhD, University of Georgia.
References
  1. Li Y, Kandasamy MK, Meagher RB. Rapid isolation of monoclonal antibodies. Monitoring enzymes in the phytochelatin synthesis pathway. Plant Physiol. 2001 Nov;127(3):711-9.
  2. LeBlanc MS, Lima A, Montello P, Kim T, Meagher RB, Merkle S. Enhanced arsenic tolerance of transgenic eastern cottonwood plants expressing gamma-glutamylcysteine synthetase. Int J Phytoremediation. 2011 Aug;13(7):657-73.
  3. Li Y, Dhankher OP, Carreira L, Balish RS, Meagher RB. Arsenic and mercury tolerance and cadmium sensitivity in Arabidopsis plants expressing bacterial gamma-glutamylcysteine synthetase. Environ Toxicol Chem. 2005 Jun;24(6):1376-86.
  4. Dhankher OP, Li Y, Rosen BP, Shi J, Salt D, Senecoff JF, Sashti NA, Meagher RB. Engineering tolerance and hyperaccumulation of arsenic in plants by combining arsenate reductase and gamma-glutamylcysteine synthetase expression. Nat Biotechnol. 2002 Nov;20(11):1140-5.
  5. Li Y, Dhankher OP, Carreira L, Lee D, Chen A, Schroeder JI, Balish RS, Meagher RB. Overexpression of phytochelatin synthase in Arabidopsis leads to enhanced arsenic tolerance and cadmium hypersensitivity. Plant Cell Physiol. 2004 Dec;45(12):1787-97. Erratum in: Plant Cell Physiol. 2005 Feb;46(2):387.

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