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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

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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

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)

SFN (Stratifin) is a Protein Coding gene

The crystal structure of this protein has been resolved to 2

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

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

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