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$711.00
$711.00
About This Item
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biological source
mouse
Quality Level
conjugate
ALEXA FLUOR™ 555
antibody form
purified immunoglobulin
antibody product type
primary antibodies
clone
22C11, monoclonal
species reactivity
canine, human, mouse, rat, porcine, monkey, fish
technique(s)
immunocytochemistry: suitable
isotype
IgG1
NCBI accession no.
UniProt accession no.
shipped in
wet ice
target post-translational modification
unmodified
Gene Information
human ... APP(351)
1 of 4
This Item | MAB348-AF647 | MAB343-C | MAB348A4 |
|---|---|---|---|
| biological source mouse | biological source mouse | biological source mouse | biological source mouse |
| antibody form purified immunoglobulin | antibody form purified antibody | antibody form purified immunoglobulin | antibody form purified immunoglobulin |
| clone 22C11, monoclonal | clone 22C11, monoclonal | clone 2.F2.19B4, monoclonal | clone 22C11, monoclonal |
| conjugate ALEXA FLUOR™ 555 | conjugate ALEXA FLUOR™ 647 | conjugate - | conjugate ALEXA FLUOR™ 488 |
| species reactivity canine, human, mouse, rat, porcine, monkey, fish | species reactivity canine, porcine, rat, fish, human, monkey, mouse | species reactivity human, mouse | species reactivity rat, pig |
| Gene Information human ... APP(351) | Gene Information human ... APP(351) | Gene Information human ... APP(351) | Gene Information human ... APP(351) |
General description
Immunogen
Application
Neuroscience
Neurodegenerative Diseases
Biochem/physiol Actions
Physical form
Preparation Note
Analysis Note
Immunocytochemistry Analysis: A 1:100 dilution of this antibody detected APP A4 in SH-5YSY cells.
Other Notes
Legal Information
Disclaimer
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Storage Class
12 - Non Combustible Liquids
wgk_germany
WGK 2
flash_point_f
Not applicable
flash_point_c
Not applicable
Certificates of Analysis (COA)
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Alzheimer’s Disease is a progressively deteriorating disease. It manifests itself with memory loss, confusion, problems with judgment, planning, concentration, and personality changes; and in it’s later stages, a decline in physical abilities. The disease’s causes, cures, and preventions are unknown; however, key proteins likely involved in the degenerative mechanism have been identified. Alzheimer’s Disease is characterized by neuronal loss, alterations in neurotransmitter systems, and the presence of neurofibrillary tangles composed of abnormally hyperphosphorylated tau proteins. A prominent feature of Alzheimer’s Disease is the formation of senile plaques in selected regions of the brain. The center of these plaques are composed mainly of fibrillary aggregates of a common, but not well understood, b amyloid peptides (Aβ). The Aβ peptides are generated from the larger amyloid-β precursor protein (APP) by the sequential action of β- and γ-secretase, and it is generally accepted that oligomeric forms of this Aβ are neurotoxic, resulting in disease progression.
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