mProX™ Human MAP3K5 Stable Cell Line
- Product Category:
- Membrane Protein Stable Cell Lines
- Subcategory:
- Kinase Cell Lines
To download a Certificate of Analysis, please enter a lot number in the search box below. Note: Certificate of Analysis not available for kit components.
Lot Number
Made to Order Inquiry
InquiryProduct Information
Product Properties
Protocols
Please visit our protocols page.
Customer Reviews
Jennifer
Verified Customer
Carol
Verified Customer
Any questions about our products? Please visit our frequently asked questions page.
Published Data
Fig.1 IHC analysis for the proteins AMACR, MAP3K5 and PDIA3.
Representative IHC images for PDIA3, MAP3K5, and AMACR are displayed. The tumor's identification was confirmed using AMARC as a marker. IHC for MAP3K5 and PDIA3 showed that both antigens were located in the cytoplasm and that tumors expressed both antigens more than normal epithelium did.
Ref: Pressinotti, Nicole Chui, et al. "Differential expression of apoptotic genes PDIA3 and MAP3K5 distinguishes between low-and high-risk prostate cancer." Molecular cancer 8.1 (2009): 1-12.
Pubmed: 20035634
DOI: 10.1186/1476-4598-8-130
Research Highlights
Longevity is linked to genetic variations of the kinase signaling gene MAP3K5. In this study, we investigate whether the longevity-association includes protection against mortality in healthy persons as well as in those with disorders associated with aging.
Morris, Brian J., et al. "Lifespan extension conferred by mitogen-activated protein kinase kinase kinase 5 (MAP3K5) longevity-associated gene variation is confined to at-risk men with a cardiometabolic disease." Aging (Albany NY) 13.6 (2021): 7953.
Pubmed:
33739303
DOI:
10.18632/aging.202844
A sub-phenotype of obesity that is harmful to metabolism is defined molecularly by AT E2F1 -ASK1. It might have a deleterious effect on AT endocrine function, which would connect AT stress to metabolic disorders throughout the body.
Haim, Yulia, et al. "ASK1 (MAP3K5) is transcriptionally upregulated by E2F1 in adipose tissue in obesity, molecularly defining a human dys-metabolic obese phenotype." Molecular metabolism 6.7 (2017): 725-736.
Pubmed:
28702328
DOI:
10.1016/j.molmet.2017.05.003