Cell Signaling Technology

Product Pathways - MAPK Signaling

MLK1 (D66E2) Rabbit mAb #5029

Applications Reactivity Sensitivity MW (kDa) Isotype
W IP H M Endogenous 120 Rabbit IgG

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

Protocols

Specificity / Sensitivity

MLK1 (D66E2) Rabbit mAb detects endogenous levels of total MLK1 protein. The antibody also cross-reacts with a 45 kDa protein of unknown origin.

Source / Purification

Monoclonal antibody is produced by immunizing animals with a synthetic peptide corresponding to residues surrounding Leu1070 of human MLK1 protein.

Western Blotting

Western Blotting

Western blot analysis of extracts from various cell lines using MLK1 (D66E2) Rabbit mAb.

Background

Mixed-lineage kinases (MLKs) belong to the mitogen activated kinase kinase kinase (MAPKKK) family of dual-specificity protein kinases. While not particularly well conserved at the sequence level, MLK1, 2 and 3 share a conserved domain structure consisting of a catalytic core and two isoleucine/leucine zipper motifs among other protein-protein binding domains (1). MLK1 preferentially stimulates the JNK (c-Jun amino-terminal kinase) pathway in response to agonists and stress (2). Although multiple phosphorylation events are required for full activation of MLK1, two autophosphorylation sites within the activation loop (Ser308 and Thr312) appear to be the predominant activation residues (3). In neuronal cells, MLK1 appears to function downstream of the small G-proteins Rac1 and Cdc42 and upstream of MKK4 and MKK7 to promote apoptosis (2).

  1. Dorow, D.S. et al. (1993) Eur J Biochem 213, 701-10.
  2. Xu, Z. et al. (2001) Mol Cell Biol 21, 4713-24.
  3. Durkin, J.T. et al. (2004) Biochemistry 43, 16348-55.

Application References

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

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