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Krebs von den Lungen-6 (KL-6)
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Cat. No.:
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KAI-250
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Type:
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Reagent
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Method:
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Immunoturbidimetric
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Format:
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Liquid
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Linearity:
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70 - 10,000 U/mL
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Sample:
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Serum, Plasma
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KIT COMPOSITION
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INTENDED USE
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For the quantitative determination of Krebs von den Lungen-6 in human serum and plasma by immunoturbidimteric assay.
FOR RESEARCH USE ONLY IN THE U.S.
NOT FOR USE IN DIAGNOSTIC PROCEDURES IN THE U.S.
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REAGENT PREPARATION
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The reagents are ready to use. They do not need to be reconstituted.
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STORAGE AND HANDLING
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All reagents should be stored refrigerated (2-8°C). Return all reagents to
2-8°C promptly after use. Unopened reagents can be used for 1 year from the
date of manufacture, as indicated by the expiration date on the package and bottle
labels. Opened reagents can be used until the expiration date if they are kept
tightly capped and at 2-8°C when not in use.
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PERFORMANCE
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Precision
With-run (Intra-assay) CV is less than 10% (n=5).
Accuracy / Correlation
A comparison of the
K-ASSAY ®
KL-6 assay and another company's KL-6 latex-enchanced immunoturbidimetric assay was performed with the following results:
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y = 1.065x - 2.3
r = 0.990
n = 122
x = another company's latex-enhanced turbidimetric KL-6 assay
y = K-ASSAY ® KL-6 assay
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An additional comparison with another company's KL-6 ECLIA (Electro Chemiluminesence Immuno-Assay) was performed with the following results:
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y = 0.973x - 172.6
r = 0.957
n = 73
x = another company's ECLIA KL-6 assay
y = K-ASSAY ® KL-6 assay
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Assay Range
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INTERFERENCE
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Bilirubin F :
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No interference up to 18.9 mg/dL
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Bilirubin C :
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No interference up to 21.3 mg/dL
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Chyle (Formazine Tubidity) :
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No interference up to 1,410
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Hemoglobin :
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No interference up to 500 mg/dL
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RF :
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No interference up to 450 IU/mL
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Sodium Citrate :
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No interference up to 150 mg/mL
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Sodium Heparin :
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No interference up to 1,500 U/mL
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EDTA-2Na :
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No interference up to 15 mg/mL
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