Rab3 Activation Assay Kit

Configuration-specific Monoclonal Antibody Based

Rab3 Activation Assay Kit

Catalog Number：82601

20 assays

Product Description

    Rab3 is a member of the Rab-family GTPases and is specifically targeted to synaptic vesicles

Currently there is no direct assay to measure the activation of Rab3 GTPases.

    NewEast Biosciences Rab3 Activation Assay Kit is based on the configuration-specific monoclonal

antibody that specifically recognizes Rab3-GTP, but not Rab3-GDP. Given the high affinity of

monoclonal antibodies to their antigens, the activation assay could be performed in a short time. This

assay provides the reliable results with consistent reproducibility.

    These anti-Rab3 -GTP monoclonal antibodies can also be used to monitor the activation of Rab3 in cells and in tissues by immunohistochemistry.

    NewEast Biosciences Rab3 Activation Assay Kit provides a simple and fast method to monitor the

activation of Rab3. Each kit provides sufficient quantities to perform 20 assays.

Assay Principle

    NewEast Biosciences Rab3 Activation Assay Kit bases on the configuration-specific anti-Rab3-GTP

monoclonal antibody to measure the active Rab3-GTP levels, either from cell extracts or from in vitro

GTPγS loading Rab3 activation assays. Briefly, anti-active Rab3 mouse monoclonal antibody will be

incubated with cell lysates containing Rab3-GTP. The bound active Rab3 will then be pulled down by

protein A/G agarose. The precipitated active Rab3 will be detected by immunoblot analysis using anti

Rab3 rabbit polyclonal antibody. 

Kit Components

1. Anti-active Rab3, Mouse Monoclonal Antibody (Catalog No. 26920): One vial – 22 µL (1

    mg/ml) in PBS, pH 7.4, containing 50% glycerol and 0.05% sodium azide. This antibody

    specifically recognizes Rab3-GTP from all vertebrates.

2. Protein A/G Agarose (Catalog No. 30301): One vial – 400 µL of 50% slurry.

3. 5X Assay/Lysis Buffer (Catalog No. 30302): One bottle – 30 mL of 250 mM Tris-HCl, pH 8, 750

    mM NaCl, 50 mM MgCl2, 5 mM EDTA, 5% Triton X-100. 

4. Anti- Rab3A, Rabbit Polyclonal Antibody (Catalog No. 21041): One vial – 100 µL (1 mg/ml)

    in PBS, pH 7.4, contained 50% glycerol.

5. 100 X GTPγS (Catalog No. 30303): One vial –100 µl at 10 mM, use 5 µL of GTPγS for

    GTP-labeling of 0.5 mL of cell lysate.

6. 100 X GDP (Catalog No. 30304): One vial –100 µl at 100 mM, use 5 µL of GDP for

    GDP-labeling of 0.5 mL of cell lysate. 

Storage

Store all kit components at 4oC until their expiration dates. 

Materials Needed but Not Supplied

1. Stimulated and non-stimulated cell lysates

2. Protease inhibitors

3. 4 °C tube rocker or shaker

4. 0.5 M EDTA, pH8.0

5. 1 M MgCl2

6. 2X reducing SDS-PAGE sample buffer

7. Electrophoresis and immunoblotting systems

8. Immunoblotting wash buffer such as TBST (10 mM Tris-HCl, pH 7.4, 0.15 M NaCl, 0.05%Tween-20)

9. Immunoblotting blocking buffer (TBST containing 5% Non-fat Dry Milk or 3% BSA)

10. PVDF or nitrocellulose membrane

11. Secondary Antibody

12. ECL Detection Reagents 

Reagent Preparation

? 1X Assay/Lysis Buffer: Mix the 5X Stock briefly and dilute to 1X in deionized water. Just prior to

usage, add protease inhibitors such as 1 mM PMSF, 10 µg/mL leupeptin, and 10 µg/mL aprotinin. 

Sample Preparation

Adherent Cells 

1. Culture cells (one 10-cm plate, ~ 10⁷cells) to approximately 80-90% confluence. Stimulate cells

    with activator or inhibitor as desired.

2. Aspirate the culture media and wash twice with ice-cold PBS.

3. Completely remove the final PBS wash and add ice-cold 1X Assay/Lysis Buffer to the cells
    (0.5- 1 mL per 10 cm tissue culture plate).

4. Place the culture plates on ice for 10-20 minutes.

5. Detach the cells from the plates by scraping with a cell scraper.

6. Transfer the lysates to appropriate size tubes and place on ice.

7. If nuclear lysis occurs, the cell lysates may become very viscous and difficult to pipette. If this

    occurs, lysates can be passed through a 27?-gauge syringe needle 3-4 times to shear the genomic     DNA.

8. Clear the lysates by centrifugation for 10 minutes (12,000 x g at 4 °C).

9. Collect the supernatant and store samples (~1-2 mg of total proteins) on ice for immediate use,

    or snap freeze and store at - 70 °C for future use. 

Suspension Cells

1. Culture cells and stimulate with activator or inhibitor as desired.

2. Perform a cell count, and then pellet the cells by centrifugation.

3. Aspirate the culture media and wash twice with ice-cold PBS.

4. Completely remove the final PBS wash and add ice-cold 1X Assay/Lysis Buffer to the cell pellet

    (0.5 – 1 mL per 1 x 10⁷cells).

5. Lyse the cells by repeated pipetting.

6. Transfer the lysates to appropriate size tubes and place on ice.

7. If nuclear lysis occurs, the cell lysates may become very viscous and difficult to pipette. If this

    occurs, lysates can be passed through a 27?-gauge syringe needle 3-4 times to shear the

    genomic DNA.

8. Clear the lysates by centrifugation for 10 minutes (12,000 x g at 4 °C).

9. Collect the supernatant and store samples on ice for immediate use, or snap freeze and store
    at -70 °C for future use. 

In vitro GTPγS/GDP Protein Loading for positive and negative controls

    Note: In vivo stimulation of cells will activate approximately 10% of the available Rab3A, whereas

in vitro GTPγS protein loading will activate nearly 90% of the Rab3A.

1. Aliquot 0.5 ml of each cell extract to two microfuge tubes (or use 1 µg of purified Rab3A protein). 

2. To each tube, add 20 µl of 0.5 M EDTA (to 20 mM final concentration).

3. Add 5 µl of 100 X GTPγS (to 100 µM, final concentration) to one tube (positive control).

4. Add 5 µl of 100 X GDP (to 1 mM, final concentration) to the second tube (negative control).

5. Incubate the tubes at 30°C for 30 minutes with agitation.

6. Stop loading by placing the tubes on ice and adding 32.5 µl of 1 M MgCl2 (to 60 mM, final

    concentration). 

Assay Procedure

I. Active Rab3 Pull-Down Assay

1. Aliquot 0.5 – 1 mL of cell lysate to a microcentrifuge tube.

2. Adjust the volume of each sample to 1 mL with 1X Assay/Lysis Buffer.

3. Add 1 µl anti-active Rab3 monoclonal antibody to the tube.

4. Thoroughly resuspend the protein A/G Agarose bead slurry by vortexing or titurating.

5. Quickly add 20 µL of resuspended bead slurry to each tube.

6. Incubate the tubes at 4 °C for 1 hour with gentle agitation.

7. Pellet the beads by centrifugation for 1 min at 5,000 x g.

8. Aspirate and discard the supernatant, making sure not to disturb/remove the bead pellet.

9. Wash the bead 3 times with 0.5 mL of 1X Assay/Lysis Buffer, centrifuging and aspirating each time.

10. After the last wash, pellet the beads and carefully remove all the supernatant.

11. Resuspend the bead pellet in 20 µL of 2X reducing SDS-PAGE sample buffer.

12. Boil each sample for 5 minutes.

13. Centrifuge each sample for 10 seconds at 5,000 x g.

II. Electrophoresis and Transfer

1. Load 15 µL/well of pull-down supernatant to a polyacrylamide gel (17%). Also, it’s

    recommended to include a pre-stained MW standard (as an indicator of a successful transfer
    instep 3).

2. Perform SDS-PAGE following the manufacturer’s instructions.

3. Transfer the gel proteins to a PVDF or nitrocellulose membrane following the manufacturer’s 

    instructions.  

III. Immunoblotting and Detection (all steps are at room temperature, with agitation)

1. Following the electroblotting step, immerse the PVDF membrane in 99% Methanol for 15

    seconds, and then allow it to dry at room temperature for 5 minutes.

    Note: If Nitrocellulose is used instead of PVDF, this step should be skipped.

2. Block the membrane with 5% non-fat dry milk or 3% BSA in TBST for 1 hr at room temperature

    with constant agitation. Incubate the membrane with anti- Rab3A polyclonal antibody, freshly
    diluted 1:50~1000 (depending on the amount of Rab3A proteins in your samples) in 5% non-fat dry     milk or 3% BSA/TBST, for 1-2 hr at room temperature with constant agitation or at 4^oC overnight.

3. Wash the blotted membrane three times with TBST, 5 minutes each time.

4. Incubate the membrane with a secondary antibody (e.g. Goat Anti-Rabbit IgG, HRP-conjugate),

    freshly diluted 1:1000 in 5% non-fat dry milk or 3% BSA/TBST, for 1 hr at room temperature

    with constant agitation.

5. Wash the blotted membrane three times with TBST, 5 minutes each time.

6. Use the detection method of your choice such as ECL. 

Example of Results

The following figure demonstrates typical results seen with NewEast Biosciences Rab3 Activation

Assay Kit. One should use the data below for reference only. 

Rab3A activation assay. Purified GST-tagged Rab3A proteins (Cat. #10128) were immunoprecipitated

with the anti-active Rab3 monoclonal antibody (Cat. No. 26920) after treated with GDP (lane 1) or

GTPγS (lane 2), and was blotted with anti-Rab3A polyclonal antibody (Cat. No. 21041). Input control is

shown in the bottom panel.