Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation
. 1978 Sep;10(5):505-15.
doi: 10.1007/BF01003133.

A quantitative method for measurement of lysosomal acid phosphatase latency in cultured rat heart cells with 210Pb

A quantitative method for measurement of lysosomal acid phosphatase latency in cultured rat heart cells with 210Pb

T W Hale et al. Histochem J. 1978 Sep.

Abstract

A method is described for measuring the latency of lysosomal acid phosphatase in cultured rat heart endotheloid cells. 210Pb was added to a medium used to demonstrate acid phosphatase activity by the Gomori lead method, and the amount of lead deposited was measured with a liquid scintillation counter. Deposition rates were measured after enzyme activation pretreatments with acetate buffer (pH 5.0) at various osmolalities, and after formaldehyde fixation. Formaldehyde, alloxan, or fluoride in the Gomori medium were evaluated for their differential effects on lysosomal and non-lysosomal acid phosphatase. The method was found to provide a sensitive, rapid and quantitative evaluation of acid phosphatase latency and should be useful for studying the integrity of lysosomes within cells.

PubMed Disclaimer

References

    1. J R Microsc Soc. 1965 Sep;84(3):361-71 - PubMed
    1. Histochem J. 1976 Jul;8(4):357-66 - PubMed
    1. Histochem J. 1975 Mar;7(2):115-26 - PubMed
    1. Anat Rec. 1951 Jan;109 (1):71-9 - PubMed
    1. J Histochem Cytochem. 1972 Jul;20(7):487-98 - PubMed

Publication types