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Invitrogen™ LRRK2 [G2019S] Recombinant Protein
Mutations in the leucine-rich repeat kinase 2 (LRRK2) gene, which codes for a multidomain protein kinase, are considered the most common genetic cause of late-onset autosomal-dominant Parkinson's disease.
Brand: Invitrogen™ A15200
Additional Details : Weight : 0.00900kg
Description
Mutations in the leucine-rich repeat kinase 2 (LRRK2) gene, which codes for a multidomain protein kinase, are considered the most common genetic cause of late-onset autosomal-dominant Parkinson's disease. This full-length, purified and active LRRK2 G2019S mutant protein may be useful in research to better understand the most common Parkinson's disease-relevant mutant, as well as to explore the mechanisms underlying the disease.Related Links:
Specifications
NP_940980.3 | |
288 kDa | |
AURA17, DARDARIN, PARK8, RIPK7, ROCO2 | |
Human | |
Store at -68 to -85°C. Aliquot at first use to avoid multiple freeze-thaws. If properly stored, this product is guaranteed for 6 months from date of purchase. Suspended in: 50 mM Tris (pH 7.5), 150 mM NaCl, 0.5 mM EDTA, 0.02% Triton™X–100, 2 mM DTT, and 50% glycerol. |
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Kinases & Inhibitors | |
Liquid |
Kinase Assay | |
10 μg | |
LRRK Kinase Family | |
DYKDDDDK | |
Mammalian | |
Recombinant, Full Length, Mutant | |
Neurobiology |