Cell Signaling Technology

Product Pathways - MAPK Signaling

MKK3b Antibody #9238

Applications Reactivity Sensitivity MW (kDa) Source
W IP H M R Endogenous 40 Rabbit

Applications Key:  W=Western Blotting  IP=Immunoprecipitation
Reactivity Key:  H=Human  M=Mouse  R=Rat
Species cross-reactivity is determined by western blot. Species enclosed in parentheses are predicted to react based on 100% sequence homology.

Protocols

Specificity / Sensitivity

MKK3b Antibody detects endogenous levels of total MKK3b protein. This antibody does not cross-react with MEK1, MEK2, MKK4 or MKK6.

Source / Purification

Polyclonal antibodies are produced by immunizing animals with a synthetic peptide corresponding to the N-terminal sequence of human MKK3. Antibodies are purified by protein A and peptide affinity chromatogrpahy.

Western Blotting

Western Blotting

Western blot analysis of extracts from C6, NIH/3T3 and 293 cells, using MKK3b Antibody #9238.

Background

MKK3 and MKK6 are two closely related dual-specificity protein kinases that activate p38 MAP kinase (1-5). MKK3 and MKK6 both phosphorylate and activate p38 MAP kinase at its activation site, Thr-Gly-Tyr, but do not phosphorylate or activate Erk1/2 or SAPK/JNK. Phosphorylation of p38 MAP kinase dramatically stimulates its ability to phosphorylate protein substrates such as ATF-2 and Elk-1. MKK3 and MKK6 are both activated by different forms of cellular stress and inflammatory cytokines (4,5). Activation of MKK3 and MKK6 occurs through phosphorylation at Ser189 and Thr222 on MKK3 (2) and Ser207 and Thr211 on MKK6 (4,5).

Three alternatively spliced transcript variants of MKK3 encoding distinct isoforms have been reported. Isoform B utilizes a different start codon compared to isoform C resulting in the production of a N-terminal segment of isoform B which is shorter and distinct from isoform C . MKK3b is the predominant form of MKK3 and strongly activates p38 MAP kinase (6)

  1. Derijard, B. et al. (1995) Science 267, 682-685.
  2. Raingeaud, J. et al. (1995) J. Biol. Chem. 270, 7420-7426.
  3. Sluss, H.K. et al. (1994) Mol. Cell. Biol. 14, 8376-8384.
  4. Raingeaud, J. et al. (1996) Mol. Cell. Biol. 16(3), 1247-1255.
  5. Han, J. et al. (1996) J. Biol. Chem. 271, 2886-2891.
  6. Han, J. et al. (1997) FEBS Letters 403(1) , 19-22.

Application References

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For Research Use Only. Not For Use In Diagnostic Procedures.

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