The Histone H1 Peptide (152-159) sequence (GGGPATP-KKAKKL-COOH) is derived from human histone H1 between amino acids 152-159 and is suitable for use as the substrate for CDK family kinase assays, such as CDK1, CDK2, CDK5 and CDK6.
Catalog No. H10-58
| Catalog No. | Pack Size | Price (USD) | |
|---|---|---|---|
| H10-58-1 | 1 mg | $83 | |
| H10-58-BULK | BULK | Contact Us |
No overview information available.
Purity:
The purity was determined to be 95.19% by HPLC analysis.
Storage, Stability and Shipping::
Store product at –20oC. For optimal storage, aliquot diluted product into smaller quantities and store at recommended temperature. For most favorable performance, avoid repeated handling and multiple freeze/thaw cycles.
Molecular Weight:
1252.53
de Pedroa Nuria et al., Protective effects of isolecanoric acid on neurodegenerative in vitro models Neuropharmacology October 2015 10.1016/j.neuropharm.2015.09.029
S Malik et al., BRCA2 mediates centrosome cohesion via an interaction with cytoplasmic dynein. Cell Cycle August 2016 10.1080/15384101.2016.1195531
Kinoshita Eiji et al., Profiling of protein thiophosphorylation by Phos-tag affinity electrophoresis: Evaluation of adenosine 5´-O-(3-thiotriphosphate) as a phosphoryl donor in protein kinase reactions Proteomics March 2014 10.1002/pmic.201300533
P Ek et al., Phosphohistidine phosphatase 1 (PHPT1) also dephosphorylates phospholysine of chemically phosphorylated histone H1 and polylysine Upsala Journal of Medical Sciences March 2014 10.3109/03009734.2014.996720
S. Darshita B et al., Identification and in vitro evaluation of new leads as selective and competitive glycogen synthase kinase-3β inhibitors through ligand and structure based drug design Journal of Molecular Graphics and Modelling July 2014 10.1016/j.jmgm.2014.06.013
Cancer, Cell Cycle, ERK/MAPK Pathway, PKA/PKC Pathway
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