catalog number :
MBS806585
products full name :
Amyloid Fibrils (OC) Antibody: ATTO 488
products short name :
[Amyloid Fibrils (OC)]
products name syn :
[OC Antibody, Fibri ls Antibody, Amyloid Oligomer afS Antibody, All Antibody, Amyloid beta A4 protein Antibody, ABPP Antibody, APPI Antibody, Alzheimer disease amyloid protein Antibody, Cerebral vascular amyloid peptide Antibody, PreA4Antibody; Protease nexin-II Antibody, APPAntibody, A4 Antibody, AD Antibody]
reactivity :
Human. Potentially mouse and rat based on species homology.
specificity :
Recognizes generic epitopes common to many amyloid fibrils and fibrillar oligomers, but not prefibrililar oligomers or natively fold proteins expect to detect in Mouse and Rat based on species homology.
purity :
Protein A Purified
form :
Protein A Purified
storage stability :
-20 degree C; 1 year + Avoid freeze/thaw cycle. Shipping: Blue Ice or 4 degree C.
tested application :
Immunoprecipitation (IP), Immunocytochemistry (ICC), Immunofluorescence (IF), Immunohistochemistry (IHC), ELISA (EIA), Western Blot (WB), Dot Blot (DB)
app notes :
1:1000 (Dot Blot)
image1 heading :
Immunohistochemistry (IHC)
image2 heading :
Immunohistochemistry (IHC)
image3 heading :
Western Blot (WB)
image4 heading :
Immunohistochemistry (IHC)
image4 description :
Immunohistochemistry analysis using Rabbit Anti-Amyloid Fibrils (OC) Polyclonal Antibody (SPC-507). Tissue: Alzheimer's Disease brain. Species: Human. Primary Antibody: Rabbit Anti-Amyloid Fibrils (OC) Polyclonal Antibody (SPC-507) at 1:100. Showing no Amyloid Precursor Protein (APP) cross-reactivity (L), but when conducted with monoclonal 6E10 (R) shows considerable APP cross-reactivity. Courtesy of: Kayed, R., Head, E., Thompson, J. L., McIntire, T. M., Milton, S. C., Cotman, C. W., et al. (2003). Common structure of soluble amyloid oligomers implies common mechanism of pathogenesis. Science 300, 486-489. doi: 10.1126/science.1079469.
image5 heading :
Dot Blot (DB)
image5 description :
Dot blot analysis using Rabbit Anti-Amyloid Fibrils (OC) Polyclonal Antibody (SPC-507). Tissue: Abeta42 fibrils and prefibrillar oligomers. Species: Human. Primary Antibody: Rabbit Anti-Amyloid Fibrils (OC) Polyclonal Antibody (SPC-507) at 1:1000. Courtesy of: Kayed, R., Head, E., Thompson, J. L., McIntire, T. M., Milton, S. C., Cotman, C. W., et al. (2003). Common structure of soluble amyloid oligomers implies common mechanism of pathogenesis. Science 300, 486-489. doi: 10.1126/science.1079469.
other info1 :
Conjugate: ATTO 488. Immunogen: Fibrils prepared from human Abeta42 peptide.
other info2 :
Storage Buffer: PBS, 50% glycerol, 0.09% sodium azide. Certificate of Analysis: A 1:1000 dilution of SPC-507 was sufficient for det ection of amyloid fibrils on PVDF membranes using transferred fiibrils by colorimetric dot blot analysis using Goat anti-rabbit IgG: HRP as the secondary antibody. Research Area: Neuroscience, Cell Signaling, Cardiovascular System, Blood. Cellular Localization: Membrane
products categories :
Neuroscience
products description :
Background Info: Recognizes generic epitopes common to many amyloid fibrils and fibrillar oligomers, but not prefibrilllar oligomers or natively folded proteins. Scientific Background: 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 (1, 2). These include the amyloid-beta peptide plaques and tau neurofibrillary tangles in senile plaques of Alzheimer's symptomology, the deposition of alpha-synuclein in the Lewy bodies of Parkinson's disease, and accumulation of polyglutamine-containing aggregates in Huntington's disease (2, 3).
products references :
1. Glabe C.G. (2004) Trends Biochem Sci. 29(10): 542-547. 2. Kayed R., et al. (2004) J Bio. Chem. 279: 46363-46366. 3. Kayed R., et al. (2003) Science. 300(5618): 486-489.