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Human Syntaxin 10, STX10 ELISA Kit, 96T Cellular Function Assays Defects in EHHADH are a
Human Syntaxin 10, STX10 ELISA Kit, 96T Cellular Function Assays Defects in EHHADH are a
Human Syntaxin 10, STX10 ELISA Kit, 96T Cellular Function Assays Defects in EHHADH are a
Human Syntaxin 10, STX10 ELISA Kit, 96T Cellular Function Assays Defects in EHHADH are a

Human Syntaxin 10, STX10 ELISA Kit, 96T Cellular Function Assays Defects in EHHADH are a

SKU: 5022438827

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SEK211.00 SEK248.00

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Human Syntaxin 10, STX10 ELISA Kit, 96T Cellular Function Assays Defects in EHHADH are a

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Description

Defects in EHHADH are a cause of peroxisomal disorders such as Zellweger syndrome

PubMed: 19805236)

Isoform 1 and isoform 2 interact with CUL5 but not with CUL1

Among its related pathways are Ribosome biogenesis in eukaryotes

Human Syntaxin 10, STX10 ELISA Kit, 96T Cellular Function Assays Defects in EHHADH are a

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