Analysis Note

Positive ControlUV treated HEK293 cells

Application

Immunoblotting (1:1000)r>Immunocytochemistry (1:200)

General description

Protein A and immunoaffinity purified rabbit polyclonal antibody. Recognizes the ~54 kDa SAPK/JNK protein.

Recognizes the ~54 kDa SAPK/JNK protein in uv-treated HEK293 cells.

This Anti-SAPK/JNK Rabbit pAb is validated for use in Immunoblotting, Immunocytochemistry for the detection of SAPK/JNK.

Immunogen

Human

a full-length, recombinant, human p54 SAPK/JNK2 fusion protein

Legal Information

TWEEN is a registered trademark of Croda International PLC

CALBIOCHEM is a registered trademark of Merck KGaA, Darmstadt, Germany

Other Notes

Recognizes SAPK/JNK regardless of the phosphorylation state. Variables associated with assay conditions will dictate the proper working dilution.r>r>Recommended Protocol for Immunoblottingr>r>Solutions and Reagentsr> Transfer Buffer: 25 mM Tris base, 0.2 M glycine, 20% methanol, pH 8.5.r> SDS Sample Buffer: 62.5 mM Tris-HCl, pH 6.8, 2% SDS, 10% glycerol, 50 mM DTT, 0.1% bromphenol blue.r> 10X TBS (Tris-buffered saline): To prepare 1 liter, 24.2 g Tris base, 80 g NaCl, adjust pH to 7.6 with HCl. Dilute 1:10 for use.r> Blocking Buffer: 1X TBS, 0.1% Tween^®-20 detergent with 5% non-fat dry milk.r> Primary Antibody Dilution Buffer: 1X TBS, 0.1% Tween™-20 detergent with 5% BSAr> Wash Buffer (TBST): 1X TBS, 0.1% Tween™-20 detergentr>r>Blotting Membraner>Nitrocellulose or PVDF membranes may be used.r>r>Protein Blottingr>A general protocol for sample preparation using 2x10⁶ 293 cells per well in a 6-well plate is as follows:r>r>1. Aspirate media. Treat cells by adding fresh media containing regulator for desired time.r>2. Aspirate media from cultures; wash cells with PBS; aspirate.r>3. Lyse cells by adding 100 µl of SDS Sample Buffer and immediately scrape the cells off the plate and transfer the extract to a microfuge tube. Keep on ice.r>4. Sonicate for 2 s to shear DNA and reduce sample viscosity.r>5. Heat sample to 95-100°C for 5 min. Cool on ice.r>6. Microcentrifuge for 5 min.r>7. Load 20 µl onto SDS-PAGE gel (10 cm x 10 cm).r>8. Electrotransfer to nitrocellulose membrane.r>r>As controls, we recommend using 20 µl lysate from UV treated HEK293 cell.r>r>Membrane Blocking, Gel and Antibody Incubationsr>1. After transfer, wash membrane with 25 ml TBS for 5 min at room temperature.r>2. Incubate membrane in 25 ml Blocking Buffer for 1-3 h at room temperature or overnight at 4°C.r>3. Wash 3 times for 5 min each with 15 ml TBST.r>4. Incubate membrane and primary antibody (at the appropriate dilution) in 10 ml Primary Antibody Dilution Buffer with gentle agitation overnight at 4°C.r>5. Wash 3 times for 5 min each with 15 ml TBST.r>6. Incubate membrane with conjugated secondary antibody at the appropriate dilution in 10 ml Blocking Buffer with gentle agitation for 1 h at room temperature.r>7. Wash membrane as in step 5.r>r>Detection of Proteinsr>Chemiluminescence.

Gupta, S., et al. 1996. EMBO J.15(11), 2760.Coso, O.A., et al. 1995. Cell81, 1137.Derijard, B., et al. 1994. Cell76, 1025.Kyriakis, J.M., et al. 1994. Nature369, 156.Hibi, M., et al. 1993. Genes Dev.7, 2135.Kyriakis, J.M. and Avruch, J. 1990. J. Biol. Chem.265, 17355.

Packaging

200 µL in Plastic ampoule

Physical form

In 150 mM NaCl, 10 mM HEPES, 50% glycerol, 0.01% BSA, pH 7.5.

Reconstitution

Following initial thaw, aliquot and freeze (-20°C).

Warning

Toxicity: Standard Handling (A)