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TBX10 Polyclonal Antibody, 20ul Plasmid Preparation Mutations of this gene have

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TBX10 Polyclonal Antibody, 20ul Plasmid Preparation Mutations of this gene haveTBX10 encodes a member of the T box family of transcription factors. These transcription factors share a DNA binding domain called the T box, and play a role in several developmental processes including early embryonic cell fate and organogenesis. The encoded protein is a member of the T box 1 subfamily. Mutations in this gene are thought to be a cause of isolated cleft lip with or without cleft palate.

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Description

Mutations of this gene have been associated with gelatinous drop-like corneal dystrophy

5 kg with platform and speed range 100-500 rpm

CHFR (checkpoint with forkhead and ring finger domains

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TBX10 Polyclonal Antibody, 20ul Plasmid Preparation Mutations of this gene haveTBX10 encodes a member of the T box family of transcription factors. These transcription factors share a DNA binding domain called the T box, and play a role in several developmental processes including early embryonic cell fate and organogenesis. The encoded protein is a member of the T box 1 subfamily. Mutations in this gene are thought to be a cause of isolated cleft lip with or without cleft palate.

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