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In Vitro Diagnostics

Immunoassay
体外診断用医薬品のイメージ画像

SLX “DP” IRMA kit

JANcode
4987797307009
Approval/Certification Number
16300AMZ00413000
Insurance Points
140
Reference Value
Reference value (reference range)
38 U/mL or less
Measurement Time
8hours

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PRODUCT FEATURES

Introduction

This product is an in vitro diagnostic reagent intended for the measurement of serum sialyl Lex-i antigen (SLX)using the IRMA (Immunoradiometric Assay) method.

Serum SLX levels have been reported to be elevated in lung cancer, pancreatic cancer, and ovarian cancer, and are considered useful as an adjunctive aid in cancer diagnosis. In particular, a high positive rate has been observed in lung adenocarcinoma, with measured values increasing with disease stage and fluctuating with treatment efficacy. In addition, the positive rate in pancreatic cancer is also high, and further improvement in diagnostic performance may be expected when used in combination with other tumor markers. Furthermore, a low false-positive rate has been reported in non-malignant diseases.

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