beta Amyloid anticorps (C-Term) (Biotin)
Aperçu rapide pour beta Amyloid anticorps (C-Term) (Biotin) (ABIN614820)
Antigène
Voir toutes beta Amyloid (Abeta) AnticorpsReactivité
Hôte
Clonalité
Conjugué
Application
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Épitope
- C-Term
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Séquence
- MVGGVVIA
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Specificité
- This antibody recognizes the C-terminal sequence (MVGGVVIA) of Aβ42 and full length Aβ42. The antibody does not cross react with amyloid beta peptide 40 in dot blotting and ELISA. Cross-reactivity to amyloid beta peptide 43 is less than 1 % in ELISA.
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Réactivité croisée (Details)
- Species reactivity (tested):Human and other primates, Mouse, Rat.
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Purification
- Protein G affinity chromatography
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Immunogène
- C-terminal of human beta amyloid peptide 42, conjugated with KLH
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Isotype
- IgG1
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Indications d'application
- Optimal working dilution should be determined by the investigator.
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Restrictions
- For Research Use only
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Format
- Liquid
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Buffer
- 0.01 M PBS, pH 7.0 ± 0.1, 0.1 % Proclin-300, 1 % Gelatin
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Agent conservateur
- Sodium azide
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Précaution d'utilisation
- This product contains sodium azide: a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.
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Conseil sur la manipulation
- Avoid repeated freezing and thawing.
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Stock
- -20 °C
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Stockage commentaire
- Store (in aliquots) at -20 °C.
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- beta Amyloid (Abeta) (Amyloid beta (Abeta))
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Autre désignation
- Amyloid beta
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Sujet
- Amyloid beta peptide 42 (Aβ42) is best known for its role in the formation of senile plaques in the brain of patients with Alzheimer's disease. Aβ42 and Aβ40 are the two major amyloid peptides that are produced after cleavage of amyloid precursor protein by secretases. Aβ42 (42 amino acids) is very fibrillogenic. The beta pleated structure of Aβ42 constituents the initial and key component of the insoluble amyloid fibril in senile plaque. It is widely accepted that Aβ42 contributes to the pathogenesis of Alzheimer's disease. One proposition is that the deposition of amyloid fibril onto the brain tissue results in Alzheimer's disease. Another is that the neurotoxicity of Aβ42 oligomer is the cause of the disease.
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ID gène
- 351
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Pathways
- Inflammasome
Antigène
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