Lambda Light Chain Kit

This product is used on NEPHSTAR® protein analysis system for quantitative determination of human LAM light chain (including free light chain and bound light chain) in serum


Catalog No
Product Catalog No: DK045

Pack Size:
Pack Size:
Pack Size:
Pack Size:
Code Name Volume/Quantity
Product Catalog No: DA045 Pack Size: LAM Antiserum Pack Size: 1×2.0 ml
Product Catalog No: DB045 Pack Size: LAM Reaction buffer Pack Size: 1×25.0 mL
Product Catalog No: DC045 Pack Size: LAM Magnetic card Pack Size: 1
Product Catalog No: DM045 Pack Size: LAM Control Pack Size: 1×0.3mL

Category:
Summary

The molecular structure of Immunoglobulin(Ig) consists of heavy chains and light chains. Five kinds of Igs have different heavy chains but have the same two kinds of light chains: Kappa and Lambda. The ratio of Kappa and Lambda is approximately 2:1. Abnormal M protein appears In sera of MM(Multiple Myeloma) patients. Because the proliferation is monoclonal and malignant, it exhibits only the increase of one type of light chain, i.e. the increase of kappa or lambda. So the measurement of light chains in blood or urine is very important for diagnosis, typing and monitoring of MM patients. In case that one type of light chain in blood or urine increases abnormally while the other type decreases, and thus the ratio of Kappa and Lambda (2:1) is changed, diagnosis as MM should be considered. Light chains may also increase in patients who suffer from autoimmune diseases, infection, tumor, acute and chronic hepatitis, hepatic cirrhosis and so on, however in these cases the kappa and Lambda increase simultaneously. Simultaneous increase of kappa and lambda chains is also observed in urine of patients suffering from nephropathy, diabetes and so on.

Test Principle

Immunonephelometry is applied. This method involves measuring the light scattered by insoluble complexes formed by reaction between specific protein in samples and its respective antiserum, and the amount of scattered light is directly proportional to the concentration of the protein under condition that antiserum is in excess. Concentrations are automatically calculated by reference to a calibration curve stored in the instrument.

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References

Lievens, M. M., J. Clin. Chem. Clin. Biochem. 27, 519-523 (1989)

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