| Code | CSB-RA001553A450phHU |
| Size | US$210 |
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| Application | Recommended Dilution |
|---|---|
| WB | 1:500-1:5000 |
AKT1, also known as protein kinase B, serves as a central node in the PI3K/AKT signaling pathway, orchestrating critical cellular decisions involving survival, proliferation, and metabolism. Phosphorylation at threonine 450 represents a key regulatory modification within the turn motif of AKT1, contributing to the kinase's proper folding and stability. Investigating this specific phosphorylation event provides researchers with valuable insights into AKT1 maturation and its functional readiness to transmit downstream signals in both normal physiology and disease states, particularly in cancer biology where AKT dysregulation is frequently observed.
This recombinant monoclonal antibody, generated from clone 2A4 in rabbit host, offers the reproducibility and consistency that demanding research requires. Because recombinant antibodies are produced from defined genetic sequences, you can expect uniform performance across different lots, eliminating the variability that can complicate long-term studies or multi-site collaborations. The antibody has been affinity-purified to ensure high specificity for the phosphorylated T450 epitope.
Validation studies demonstrate reliable performance in Western blot applications, where the antibody successfully detected phospho-AKT1 in HeLa whole cell lysate at the expected molecular weight of 60 kDa, confirming accurate target recognition. The recommended working dilution range of 1:500 to 1:5000 for Western blot provides flexibility to optimize signal intensity based on your specific experimental conditions and sample abundance. The antibody is also validated for ELISA, expanding its utility across different experimental workflows.
For researchers investigating signal transduction mechanisms, particularly those focused on AKT pathway regulation and phosphorylation-dependent signaling events in human samples, this antibody provides a dependable tool for detecting this functionally significant modification.
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