SensoLyte® Thioflavin T ß-Amyloid (1-42) Aggregation Kit - 1 kit
Kaneka Eurogentec S.A.
SKU / CAT#: AS-72214
$60300
usd
$603.00/kit
AS-72214

SensoLyte® Thioflavin T ß-Amyloid (1-42) Aggregation Kit - 1 kit

Kaneka Eurogentec S.A.
$60300
usd
$603.00/kit
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Available
SHIPS May 9th
Available
SHIPS May 9th
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Description
The SensoLyte® ThT β-Amyloid (1-42) Aggregation kit provides a convenient and standard method to measure Aβ42 aggregation using Thioflavin T dye. Aβ42 peptide is pretreated to ensure it is in a monomeric state. An optimized fibrillation buffer is included with the kit, and two known inhibitors are supplied as controls. The assay is based on the property of ThT dye in which fluorescence (Ex/Em=440/484 nm) is increased when bound to aggregated Aβ peptides. Alzheimer's disease (AD), the most common cause of dementia, is characterized by the presence of senile plaques and neurofibrillary tangles,...
The SensoLyte® ThT β-Amyloid (1-42) Aggregation kit provides a convenient and standard method to measure Aβ42 aggregation using Thioflavin T dye. Aβ42 peptide is pretreated to ensure it is in a monomeric state. An optimized fibrillation buffer is included with the kit, and two known inhibitors are supplied as controls. The assay is based on the property of ThT dye in which fluorescence (Ex/Em=440/484 nm) is increased when bound to aggregated Aβ peptides. Alzheimer's disease (AD), the most common cause of dementia, is characterized by the presence of senile plaques and neurofibrillary tangles,...
Shipping & Handling
Shipped In
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Safety & Storage
Storage Temperature
Store kit components at 4°C. Components B, D, and E should be stored at -20°C if not used within one week
Safety Statement
This product is for research or laboratory use only and are not to be administrated to humans. This product is not intended for medical diagnostic or therapeutic use.
Regulatory & Compliance
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Specifications
CLASS
Alzheimer's Disease
COUNTRY OF ORIGIN
United States of America
APPLICATION
Aggregation/Fibrillation
UNIPROT ID
P05067
NACRES
NA.32
*USAGE / SAFETY STATEMENT
This product is for research or laboratory use only and are not to be administrated to humans. This product is not intended for medical diagnostic or therapeutic use.
DISCLAIMER
Labscoop LLC and/or Kaneka Eurogentec S.A.'s liability shall be limited strictly to the replacement of non-compliant products or to the reimbursement of their price, at Labscoop LLC and/or Kaneka Eurogentec S.A.'s sole election. To the full extent permissible under the applicable legislation Labscoop LLC nor Kaneka Eurogentec S.A. may not be held liable for any cost or liability arising from or in connection with this product, including damages or accidents to persons, damages to goods other than this product sold, loss of earnings or profits, harm to reputation, or any other prejudice arising directly or indirectly from the product, and including defective products. IN NO EVENT SHALL LABSCOOP LLC OR KANEKA EUROGENTEC S.A. BE LIABLE UNDER THIS AGREEMENT FOR ANY PUNITIVE, EXEMPLARY, INDIRECT OR CONSEQUENTIAL DAMAGES, INCLUDING LOST PROFITS. This product ordered by the customer are exclusively intended for laboratory research purposes and shall correspond to the quality and safety standards in accordance with said research purposes. This product shall not be used by the customer for any other purposes such as (the list is not exhaustive) diagnostic, prophylactic, therapeutic, cosmetic, commercial ends, or as food, ingredients or medical devices. Labscoop LLC and Kaneka Eurogentec S.A. shall accept no liability if the customer who ordered this product, intended exclusively for laboratory research, uses this product for purposes other than for research.
QUALITY CERTIFICATION / COMPLIANCE
Eurogentec Quality Management System is ISO 9001 certified by BSI under certificate number FS 638601. The certification applies to following activities: “Development, production and sales of products and services for research and development in life sciences”. Regulations for in vitro diagnostics (IVD) - Eurogentec manufactures products in support of in vitro diagnostic and related applications. The IVD medical device industry is regulated by FDA GMP/QSR (21 CFR Part 820), EU IVD Directive 98/79 EEC and EU 2017/746 Regulation. These regulations are not applicable to Eurogentec as it does not manufacture medical devices. However Eurogentec quality system is compliant to the applicable quality system requirements of these regulations.
DETECTION METHOD
Fluorescent
KIT COMPONENTS
Component A: Assay Buffer: 25 ml Component B: Beta-Amyloid (1-42) (Aß42), human: 0.5 mg (2 x 0.25 mg, net peptide) Component C: Thioflavin T (ThT): 20 mM, 100 µl Component D: Morin: 20 mM, 25 µl Component E: Phenol Red: 20 mM, 25 µl
RESEARCH AREA
Neuroscience Peptide & Protein Analysis
ABSORBANCE
440
EMISSIONS
484
BIOMARKER TARGET
beta-amyloid beta-amyloid (1-42) Thioflavin T
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SensoLyte® Thioflavin T ß-Amyloid (1-42) Aggregation Kit - 1 kit
SensoLyte® Thioflavin T ß-Amyloid (1-42) Aggregation Kit - 1 kit
Shipping & Handling
Shipped In
Cold Packs
Safety & Storage
Storage Temperature
Store kit components at 4°C. Components B, D, and E should be stored at -20°C if not used within one week
Safety Statement
This product is for research or laboratory use only and are not to be administrated to humans. This product is not intended for medical diagnostic or therapeutic use.
Regulatory & Compliance
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