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Fig. 5 | BMC Genomics

Fig. 5

From: An autosomal recessive variant in PYGM causes myophosphorylase deficiency in Red Angus composite cattle

Fig. 5

A Longitudinal section with immunohistochemical stain for myophosphorylase protein (red color) in a wild-type calf. B Longitudinal immunohistochemical stain for myophosphorylase protein in an affected calf shows no staining for myophosphorylase. C Histochemical stain for myophosphorylase activity in a control calf with blue staining indicating active myophosphorylase enzyme. D Histochemical stain for myophosphorylase activity in an affected calf with lack of staining indicating no myophosphorylase enzyme activity

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BMC Genomics

ISSN: 1471-2164

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