Recombinant Amyloid beta Antibody / APP
Proteolytic cleavage of the Amyloid protein precursor (APP) gives rise to the beta-Amyloid and Amyloid A4 proteins, which are present in human platelets. Amyloid deposition is associated with type II diabetes, Down syndrome and a variety of neurological disorders, including Alzheimer s disease. The Amyloid precursor protein (APP) undergoes alternative splicing, resulting in several isoforms. Proteolytic cleavage of APP leads to the formation of the 4 kDa Amyloid beta/A4 Amyloid protein. This protein is involved in the formation of neurofibrillary tangles and plaques that characterize the senile plaques of Alzheimer s patients. APLP1 (Amyloid precursor-like protein 1) and APLP2 are structurally similar to APP. Human APLP2 is a membrane-bound sperm protein that contains a region highly homologous to the transmembrane-cytoplasmic domains of APP found in brain plaques of Alzheimer s disease patients.
Product Specifications
Specifications
Immunohistochemistry (FFPE) : 1-2 µg/mL
UniProt
P05067
Host
Rabbit
Reactivity
Human
Immunogen
A portion of amino acids 500-700 from human APP protein was used as the immunogen for the recombinant Amyloid beta antibody.
Clonality
Recombinant Monoclonal
Isotype
IgG κ
Clone
APP/9971R
Applications
IHC-P
Purity
Protein A affinity
Format
Purified
Limitations
This recombinant Amyloid beta antibody is available for research use only.
Storage Conditions
Aliquot the recombinant Amyloid beta antibody and store frozen at -20°C or colder. Avoid repeated freeze-thaw cycles.
Formulation
1 mg/mL in 1X PBS; BSA free, sodium azide free
Applications Notes
Optimal dilution of the recombinant Amyloid beta antibody should be determined by the researcher.
Location
Membrane, cytoplasm
Image Legend
Explore Other Products
Discover premium biology products from our extensive collection of 20M+ items