标题：免疫共沉淀（Protein A Agarose）试剂盒

迈晨科技 免疫共沉淀反应 （Protein A Agarose）试剂盒

mmunoprecipitation Kit   Protein A Agarose

免疫共沉淀反应 （Protein A Agarose）试剂盒

Description:

Anti-FLAG affinity gel is a purified mouse IgG1 monoclonal antibody covalently conjugated to agarose by hydrazide linkage. The kit is designed for purification or immunoprecipitation of FLAG-tagged proteins from a variety of sources including mammalian cells, insect cells, bacteria and plant.

Size: 30 standard assays

Kit components:

Components      Name      Cat#      Size

Component A      Protein A Agarose      IR003      1mL

Component B      Binding Buffer      MP011      50mL

Component C      Washing Buffer (5X)      MP011T      50mL

Component D      Elution Buffer      MP005      1.5mL

Component E      Neutralization Buffer      MC030.2      0.5mL

Precedures:

A.      Preparation of Cell Lysates (for adherent mammalian cells)

1.      Remove the growth medium from the cells to be analyzed. Rinse the cells twice with PBS buffer (Cat# CC008).

2.      Add 10ml (10-cm plate), scrape the cells off the plate and transfer cells into 15-cm Folcon tube.

3.      Centrifuge the sample at 1000 x g for 5 mins.

4.      Discard the PBS, add lysis buffer (Cat# MP011T) (106-107 cells/ml).

5.      Incubate the cells for 15-30 minutes on a shaker.

6.      Centrifuge the cell lysate for 10 minutes at 12,000 x g.

7.      Transfer the supernatant to a 1.5ml eppendorf tube.

8.      For immediate use, keep on ice. If the supernatant is not to be used immediately, store it at –70 °C.

B.      Immunoprecipitation of FLAG-tagged Proteins

1.      Thoroughly suspend the Anti-FLAG affinity agarose beads.

2.      Transfer 30ul of the gel suspension to a 1.5ml eppendorf tube. (For beads transfer, use plastic pipette tip with the end cut for about 2mm to allow the beads to be transferred).

3.      Centrifuge the beads briefly to bring the beads to the bottom of the tube.

4.      Wash the beads twice with 0.5 ml 1X Washing Buffer.

5.      Add 500-1000ul of cell lysates (up to 1mg) to the beads. The lysates could be diluted with Binding Buffer.

C.      Elution

Elution with 0.1 M glycine HCl, pH 3.5

1.      Add 100ul Elution Buffer to each sample.

2.      Incubate the samples and controls with gentle shaking for 5 minutes at room temperature.

3.      Centrifuge the beads for 30 seconds at 5,000 x g. Transfer the supernatants to a new tube containing 10ul Neutralization Buffer.

Note: The procedure should be performed at room temperature. Do not leave the beads in this buffer >20 minutes.

Elution with SDS-PAGE Sample Loading Buffer

1.      Add 20ul of 2X sample loading buffer (Cat# MP006.1) to each sample.

2.      Boil the samples for 5 minutes.

3.      Briefly votex the tube and centrifuge the samples at 5,000 x g for 30 seconds to pellet agarose.

4.      Transfer the supernatants to a new tube.

5.      The samples are ready for loading on SDS-PAGE and immunoblotting using Anti-FLAG or specific antibodies against the fusion protein or associated proteins.

Note: The procedure should be preformed at room temperature. Sample buffer should be at room temperature before use

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