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Human/Rat β Amyloid (42) ELISA Kit Wako, High Sensitive Data

Performance

Standard curve

Normal Human Plasma (A-H) were measured using the ELISA Kit Wako Ⅱand the conventional kit. The obtained results were equivalent for the two kits.


Spike-and-recovery-test

Standard curves were prepared using the standard solution included in the kit.


Dilution linearity test

Normal Human Plasma (A, C, E) were diluted 2-16 folds to determine the dilution linearity. Human/Rat Aβ exhibited linear dilution.

Specificity test

Sample Cross-reactivity (%)
Human Aβ (1-40) ≦ 0.1
Human Aβ (1-42) 100.0
Human Aβ (1-43) 12.7
Rat (Mouse) Aβ (1-40) ≦ 0.1
Rat (Mouse) Aβ (1-42) 156.0

 

Application Data

Measurements in human and mouse plasma

Blood samples collected in evacuated blood collection tubes with K2EDTA were centrifuged for 15 min. at 5,000 x g and 4°C. Plasma was isolated and kept in -80°C until use.

The plasma samples were diluted 4-fold using the standard dilution solution contained in the kit prior to the measurements.

(※Human β Amyloid (1-40) ELISA Kit Wako II (Catalog ID 298-64601) and Human/Rat β Amyloid (40) ELISA Kit Wako II (Catalog ID 294-64701) were used for the measurements of Aβ [1-40] and Aβ [x-40]).


Measurements in the mouse brain

The brain hemisphere of a 12-week-old APP transgenic mouse (J20) was homogenized with 2 mL Tris-buffered Saline and kept in -20°C until use.

The extract was diluted 2-fold using the standard diluent solution contained in the kit prior to the measurements.

A small amount of Aβ was detected in samples from both transgenic (tg) and wild-type (wt) mice.

(Data provided by: Drs. Iwatsubo and Hashimoto, Department of Neuropathology, Graduate School of Medicine, University of Tokyo)

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