Anti-p38 MAP Kinase (341-360) Rabbit pAb

Protein A and immunoaffinity purified rabbit polyclonal antibody. Recognizes the ~38 kDa p38 MAPK protein.

Recognizes the ~38 kDa p38 MAPK protein.

Antibody Target Gene Symbol: MAPK14

Target Synonym: CRK1, CSBP, CSBP1, CSBP2, CSPB1, EXIP, Hog, MAPK p38, MGC102436, MGC105413, MXI2, P38, P38 KINASE, P38 Map Kinase, p38 Mapk alpha, P38-ALPHA, p38-RK, p38/Hog1, p38/Mpk2, P38/RK, p38a, p38Hog, p38MAPK, PRKM14, PRKM15, RK, SAPK2A

Entrez Gene Name: mitogen-activated protein kinase 14

Hu Entrez ID: 1432

Mu Entrez ID: 26416

Rat Entrez ID: 81649

This Anti-p38 MAP Kinase (341-360) Rabbit pAb is validated for use in Flow Cytometry, Immunoblotting, Paraffin Sections for the detection of p38 MAP Kinase (341-360).

Human

a synthetic peptide (TYDEYISFVPPPLDQEEMES) corresponding to amino acids 341-360 of human p38 MAP kinase

Flow Cytometry (1:25)

Immunoblotting (1:1000)

Paraffin Sections (1:50, heat pretreatment required, see comments)

Toxicity: Standard Handling (A)

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

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

Pretreat paraffin sections by heating tissue in 10 mM citrate buffer, pH 6.0 for 1 min at high power followed by 9 min at medium power; keep the slides fully immersed and maintain the temperature at or just below boiling; cool the slides for 20 min at room temperature prior to staining. Variables associated with assay conditions will dictate the proper working dilution.



Recommended Protocol for Immunoblotting



Solutions and Reagents

• Transfer Buffer: 25 mM Tris base, 0.2 M glycine, 20% methanol, pH 8.5.

• SDS Sample Buffer: 62.5 mM Tris-HCl, pH 6.8, 2% SDS, 10% glycerol, 50 mM DTT, 0.1% bromophenol blue.

• 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.

• Blocking Buffer: 1X TBS, 0.1% Tween^®-20 detergent with 5% non-fat dry milk.

• Primary Antibody Dilution Buffer: 1X TBS, 0.1% Tween-20 detergent with 5% BSA

• Wash Buffer (TBST): 1X TBS, 0.1% Tween-20 detergent



Blotting Membrane

Nitrocellulose or PVDF membranes may be used.



Protein Blotting

1. Lyse cells by adding 100 ml SDS Sample Buffer and immediately scrape the cells off the plate and transfer the extract to a microfuge tube. Keep on ice.

2. Sonicate for 2 s to shear DNA and reduce sample viscosity.

3. Heat sample to 95-100°C for 5 min. Cool on ice.

4. Microcentrifuge for 5 min.

5. Load 20 ml onto SDS-PAGE gel (10 cm x 10 cm).

6. Electrotransfer to nitrocellulose membrane.



As controls, we recommend using 15 ml of phosphorylated and nonphosphorylated C-6 glioma cell extracts.



Membrane Blocking, Gel and Antibody Incubations

1. After transfer, wash membrane with 25 ml TBS for 5 min at room temperature.

2. Incubate membrane in 25 ml of Blocking Buffer for 1-3 h at room temperature or overnight at 4°C.

3. Wash 3 times for 5 min each with 15 ml TBST.

4. Incubate membrane and primary antibody (at the appropriate dilution) in 10 ml Primary Antibody Dilution Buffer with gentle agitation overnight at 4°C.

5. Wash 3 times for 5 min each with 15 ml TBST.

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.

7. Wash membrane as in step 5.



Detection of Proteins

Chemiluminescence.

Raingeaud, J., et al. 1995. J. Biol. Chem.270, 7420.
Zervos, A.S., et al. 1995. Proc. Natl. Acad. Sci. USA92, 10531.
Han, J., et al. 1994. Science265, 808.
Lee, J.C., et al. 1994. Nature372, 739.
Rouse, J., et al. 1994. Cell78, 1027.

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