GST-Catcher

N° du produit ABIN5311506

Détail du produit

Antigène: GST (Glutathione S Transferase (GST))

Reactivité: Schistosoma japonicum

Application: Protein Complex Immunoprecipitation (Co-IP), Immunoprecipitation (IP), Purification (Purif), Chromatin Immunoprecipitation (ChIP), RNA-Binding Protein Immunoprecipitation (RIP)

Type d'échantillon: Cell Extracts

Specificité: The Antibody with Clone G19 recognizes Schistosoma japonicum Glutathione S-transferase (GST)

Attributs du produit: GST-Catcher is based on a high-affinity single-domain antibody (sdAb) that is covalently immobilized on 4 % cross-linked agarose beads. The innovative, oriented and selective attachment via a flexible linker guarantees a high accessibility of the sdAbs and largely eliminates batch-to-batch variations. Due to the single-chain nature of sdAbs and their covalent attachment, no "leakage" of light and heavy chains from IgGs is observed during elution with SDS sample buffer. GST-Catcher thus features high affinity and superior capacity for GST fusion proteins while showing negligible non-specific background. GST-Catcher is compatible not only with physiological buffers but also with high stringency buffers. GST-Catcher thus provides great freedom to adjust the binding and washing conditions to the experimental needs.

Ingrédients: 4 % cross-linked agarose (bead size 50-150 μm) with covalently immobilized single-domain antibody

Matériel non inclus: wash buffers, columns, tubes

Bead Ligand: Antibody

Bead Matrix: Agarose beads

Bead Size: 90 μm

Information d'application

Indications d'application: 200 μL slurry for up to 10 reactions

Commentaires:

Capacity: > 2.5 μg GST per μl of packed beads

Protocole:

This protocol provides a general outline of how to use GST-Catcher (agarose beads) for immunoprecipitation using a microcentrifuge for sedimentation. Alternatively, it is possible to use GST-Catcher agarose beads in spin columns. All protocol steps should be carried out at 4 °C.

1. For mammalian cells, harvest 10⁶-10⁸ cells per sample.
2. Lyse cells according to established protocols in 0.2 to 1.5 mL volume. Recommended Buffer Conditions: GST-Catcher resins are compatible with commonly used Lysis and Washing buffers, e.g. RIPA buffer. The following buffer conditions have been tested:
   
   • pH ranging from pH 5 to pH 9
   • 2 % Triton X-100, 1 % Tween-20, 1 % NP-40, 1 % CHAPS, 1 % Deoxycholate, 0.1 % SDS
   • 4 M NaCl, 2 M KCl, 1 M MgCl₂
   • 100 mM EDTA
   • 4 M urea
   • 10 mM DTT, 10 mM 2-Mercaptoethanol
   • Protease Inhibitors
   • RNAse A, DNAse I, Benzonase
3. Centrifuge cell lysates in microcentrifuge tubes for 10 min at 14.000 x g at 4 °C. Keep a small samples as “input” fraction.
4. Transfer the supernatant to a fresh microcentrifuge tube for each sample and keep at 4 °C.
5. Homogenize the GST-Catcher (agarose beads) slurry gently by shaking.
6. Transfer 20 μL bead slurry to a 1.5 mL microcentrifuge tube for each sample.
7. Add 1 mL Lysis Buffer to equilibrate GST-Catcher (agarose beads).
8. Centrifuge GST-Catcher (agarose beads) for 1 min at 1000 x g and carefully remove the supernatant.
9. Repeat wash steps once for a total of two washes.
10. Resuspend equilibrated GST-Catcher (agarose beads) gently with the cell lysate supernatant.
11. Rotate the microcentrifuge tubes for 1 h at 4 °C.
12. Centrifuge microcentrifuge tubes for 1 min at 1000 x g at 4 °C. Keep a small sample as “unbound” fraction. Carefully remove the supernatant.
13. Resuspend GST-Catcher (agarose beads) in 1 mL Lysis Buffer.
14. Centrifuge GST-Catcher (agarose beads) for 1 min at 1000 x g and carefully remove the supernatant.
15. Repeat wash steps twice for a total of three washes.
16. Resuspend GST-Catcher (agarose beads) gently in 1 mL TBS.
17. Centrifuge GST-Catcher (agarose beads) for 1 min at 1000 x g and carefully remove the supernatant.
18. Resuspend GST-Catcher (agarose beads) gently in 1 mL TBS.
19. Centrifuge GST-Catcher (agarose beads) for 1 min at 3000 x g and carefully remove the supernatant.
20. Resuspend GST-Catcher (agarose beads) resin in 50 µL 2X SDS samples buffer.
21. Heat GST-Catcher (agarose beads) resin for 5 min to 95 °C.
22. Centrifuge microcentrifuge tubes for 1 min at 3000 x g and transfer the supernatant to fresh microcentrifuge tubes. Keep the GST-Catcher (agarose beads) as backup.

Restrictions: For Research Use only

Stockage

Buffer: 50 % slurry in 20 % ethanol / PBS 0.09 % sodium azide

Agent conservateur: Sodium azide

Précaution d'utilisation: This product contains Sodium azide: a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.

Stock: 4 °C

Détail du antigène

Antigène: GST (Glutathione S Transferase (GST))

Autre désignation: Glutathione S-transferase (GST) (GST Produits)

Synonymes: GST Bead, GST 13-13 Bead, GST13 Bead, GST13-13 Bead, GSTK1-1 Bead, hGSTK1 Bead, 1500002K10Rik Bead, Gst Bead, Ptgds2 Bead, glutathione S-transferase kappa 1 Bead, microsomal glutathione S-transferase 1 Bead, hematopoietic prostaglandin D synthase Bead, GSTK1 Bead, Mgst1 Bead, Hpgds Bead

Sujet: Glutathione S-transferase (GST) from Schistosoma japonicum is a 26 kDa enzyme, often found as a fusion partner in expression systems. GST folds rapidly and boosts the expression and the folding of the fusion partner. It is also used as purification tag wi