T8451
Monoclonal Anti-Tau, First N-terminal Insert antibody produced in mouse
clone DC 39N1, purified immunoglobulin, buffered aqueous solution
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About This Item
UNSPSC Code:
12352203
MDL number:
biological source
mouse
conjugate
unconjugated
antibody form
purified immunoglobulin
antibody product type
primary antibodies
clone
DC 39N1, monoclonal
form
buffered aqueous solution
mol wt
antigen 45-68 kDa
species reactivity
human
technique(s)
immunohistochemistry: 1:1,000, indirect ELISA: 1:2,000, western blot: 1:2,000
isotype
IgG1
UniProt accession no.
shipped in
dry ice
storage temp.
−20°C
Gene Information
human ... MAPT(4137)
Immunogen
first tau insert (N1).
Physical form
Solution in serum-free DMEM (without sodium pyruvate and sodium bicarbonate) containing 0.1% thimerosal as a preservative.
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.
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signalword
Warning
hcodes
pcodes
Hazard Classifications
STOT RE 2
target_organs
Kidney
Storage Class
10 - Combustible liquids
wgk
WGK 1
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
Eyeshields, Faceshields, Gloves, type ABEK (EN14387) respirator filter
Regulatory Information
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Related Content
Instructions
Novel Anti-tau Monoclonal antibody With Specificity for NI Terminal Insert.
Mikulova K, et al.,
Neurobiology of Aging, 25, S432-S434 (2004)
Giuseppina Amadoro et al.
Journal of Alzheimer's disease : JAD, 21(2), 445-470 (2010-06-24)
Synapses are ultrastructural sites for memory storage in brain, and synaptic damage is the best pathologic correlate of cognitive decline in Alzheimer's disease (AD). Post-translational hyperphosphorylation, enzyme-mediated truncation, conformational modifications, and aggregation of tau protein into neurofibrillary tangles (NFTs) are
Veronica Corsetti et al.
Brain communications, 2(1), fcaa039-fcaa039 (2020-09-22)
Clinical and neuropathological studies have shown that tau pathology better correlates with the severity of dementia than amyloid plaque burden, making tau an attractive target for the cure of Alzheimer's disease. We have explored whether passive immunization with the 12A12