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Amyloid Oligomers (A11) Antibody (APC)

Rabbit polyclonal to Amyloid Oligomers (APC) . Amyloid monomeric proteins can sometimes oligomerize into destructive amyloid fibrils. Amyloidogenic conformations of non-disease related proteins can be created by partial protein misfolding or denaturation. Many degenerative diseases are known to be related to the accumulation of misfolded proteins as amyloid fibres. These include the amyloid- beta peptide plaques and tau neurofibrillary tangles in senile plaques of Alzheimers symptomology, the deposition of alpha-synuclein in the Lewy bodies of Parkinsons disease, and accumulation of polyglutamine-containing aggregates in Huntingtons disease.

Product Specifications

Product Name Alternative

Amyloid Oligomer alpha beta, A11, Amyloid Oligomer AlphaBeta, APP, Amyloid beta A4 protein, ABPP, APPI, Alzheimer disease amyloid protein, Cerebral vascular amyloid peptide, PreA4, Protease nexin-II, A4, AD1

UniProt

P05067

Reactivity

Human, Mouse, Other, Rat

Immunogen

Synthetic molecular mimic of soluble oligomers

Target

Amyloid Oligomers (A11)

Clonality

Polyclonal

Conjugation

APC

Field of Research

Neuroscience; Immunology & Inflammation

Purification

Protein A Purified

Dilution

The suggested dilution for the current lot of SPC-506 in Western Blot and Dot Blot is 1:100

Storage Conditions

Conjugated antibodies should be stored according to the product label

Notes

For research use only.

Applications Notes

A 1:200 dilution was sufficient for detection of amyloid oligomers in 10 μg of mouse brain lysates by colorimetric immunoblot analysis using Goat anti-rabbit IgG:HRP as the secondary antibody.

Tested Applications

ELISA, ICC, IF, IHC, IP, WB

NCBI Accession Number

NM_000484.2

Host or Source

Rabbit

Preservative

95.46mM Phosphate, 2.48mM MES and 2mM EDTA

Entrez

8666

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