Canine aldosterone,ALD ELISA K

Canine aldosterone,ALD ELISA Kit

PRINCIPLE OF THE ASSAY
This assay employs the quantitative sandwich enzyme immunoassay technique.
Antibody specific for ALD has been pre-coated onto a microplate. Standards and
samples are pipetted into the wells and any ALD present is bound by the
immobilized antibody. After removing any unbound substances, a
biotin-conjugated antibody specific for ALD is added to the wells. After washing,
avidin conjugated Horseradish Peroxidase (HRP) is added to the wells.
Following a wash to remove any unbound avidin-enzyme reagent, a substrate
solution is added to the wells and color develops in proportion to the amount of
ALD bound in the initial step. The color development is stopped and the intensity
of the color is measured.

Canine aldosterone,ALD ELISA Kit

DETECTION RANGE
12.5 pg/ml-800 pg/ml.

Canine aldosterone,ALD ELISA Kit

SENSITIVITY
The minimum detectable dose of canine ALD is typically less than 3.12 pg/ml.
The sensitivity of this assay, or Lower Limit of Detection (LLD) was defined as
the lowest protein concentration that could be differentiated from zero. It was
determined the mean O.D value of 20 replicates of the zero standard added by
their three standard deviations.

Canine aldosterone,ALD ELISA Kit

SPECIFICITY
This assay has high sensitivity and excellent specificity for detection of canine
ALD. No significant cross-reactivity or interference between canine ALD and
analogues was observed.
Note: Limited by current skills and knowledge, it is impossible for us to complete
the cross-reactivity detection between canine ALD and all the analogues,
therefore, cross reaction may still exist.

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PRECISION
Intra-assay Precision (Precision within an assay): CV%<8%
Three samples of known concentration were tested twenty times on one plate to
assess.
Inter-assay Precision (Precision between assays): CV%<10%
Three samples of known concentration were tested in twenty assays to assess.
LIMITATIONS OF THE PROCEDURE
 FOR RESEARCH USE ONLY. NOT FOR USE IN DIAGNOSTIC
PROCEDURES.
 The kit should not be used beyond the expiration date on the kit label.
 Do not mix or substitute reagents with those from other lots or sources.
 If samples generate values higher than the highest standard, dilute the
samples with Sample Diluent and repeat the assay.
 Any variation in Sample Diluent, operator, pipetting technique, washing
technique, incubation time or temperature, and kit age can cause variation
in binding.
 This assay is designed to eliminate interference by soluble receptors,
binding proteins, and other factors present in biological samples. Until all
factors have been tested in the Immunoassay, the possibility of
interference cannot be excluded.