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biological source
human
Quality Level
Assay
>90% (SDS-PAGE)
form
powder
manufacturer/tradename
Chemicon®
NCBI accession no.
UniProt accession no.
shipped in
dry ice
General description
Tau-441
MOL. WT.: 45,900
PEPTIDE CONTENT: 50 μg per vial (protein content and concentration determined by BCA protein assays using BSA as standard).
COUNTER ION: Lyophilized in final buffer of 50 mM MES, pH 6.8, 100 mM NaCl and 0.5 mM EGTA.
MOL. WT.: 45,900
PEPTIDE CONTENT: 50 μg per vial (protein content and concentration determined by BCA protein assays using BSA as standard).
COUNTER ION: Lyophilized in final buffer of 50 mM MES, pH 6.8, 100 mM NaCl and 0.5 mM EGTA.
Application
Research Category
Neuroscience
Neuroscience
Research Sub Category
Neurodegenerative Diseases
Neurodegenerative Diseases
Physical form
White lyophilized powder. Resuspend in water at a concentration of 1 mg/mL. This will give you a final of 50 mM MES, pH 6.8, 100 mM NaCl and 0.5 mM EGTA.
Storage and Stability
Maintain lyophilized material at -20ºC for up to 12 months after date of receipt. After reconstitution maintain at -20ºC to -70ºC for up to 2 weeks in undiluted aliquots. Avoid freeze/thaw cycles to avoid aggregation.
Legal Information
CHEMICON is a registered trademark of Merck KGaA, Darmstadt, Germany
Disclaimer
Unless otherwise stated in our catalog or other company documentation accompanying the product(s), our products are intended for research use only and are not to be used for any other purpose, which includes but is not limited to, unauthorized commercial uses, in vitro diagnostic uses, ex vivo or in vivo therapeutic uses or any type of consumption or application to humans or animals.
WGK
WGK 1
Certificates of Analysis (COA)
Search for Certificates of Analysis (COA) by entering the products Lot/Batch Number. Lot and Batch Numbers can be found on a product’s label following the words ‘Lot’ or ‘Batch’.
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Find documentation for the products that you have recently purchased in the Document Library.
Tau seeding and spreading in vivo is supported by both AD-derived fibrillar and oligomeric tau.
Mate De Gerando, et al.
Acta neuropathologica, 146, 191-210 (2023)
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