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Human Syntaxin 10, STX10 ELISA Kit, 96T Cellular Function Assays PubMed: 19805236)
Human Syntaxin 10, STX10 ELISA Kit, 96T Cellular Function Assays PubMed: 19805236)
Human Syntaxin 10, STX10 ELISA Kit, 96T Cellular Function Assays PubMed: 19805236)
Human Syntaxin 10, STX10 ELISA Kit, 96T Cellular Function Assays PubMed: 19805236)

Human Syntaxin 10, STX10 ELISA Kit, 96T Cellular Function Assays PubMed: 19805236)

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Human Syntaxin 10, STX10 ELISA Kit, 96T Cellular Function Assays PubMed: 19805236)

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Description

PubMed: 19805236)

Probable metal transporter

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

Degradation of intravascular NETs by DNASE1 and DNASE1L3 is required to prevent formation of clots that obstruct blood vessels and cause organ damage following inflammation (By similarity)

Among its related pathways are Ribosome biogenesis in eukaryotes

Human Syntaxin 10, STX10 ELISA Kit, 96T Cellular Function Assays PubMed: 19805236)

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