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MyoD Polyclonal Antibody, 100ul[BT-AP05723] 3D Culture Mutations in SLC16A2 are the

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MyoD Polyclonal Antibody, 100ul[BT-AP05723] 3D Culture Mutations in SLC16A2 are theMYO9B encodes a member of the myosin family of actin based molecular motor heavy chain proteins. The protein represents an unconventional myosin; it should not be confused with the conventional non muscle myosin 9 (MYH9). The protein has four IQ motifs located in the neck domain that bind calmodulin, which serves as a light chain. The protein complex has a single headed structure and exhibits processive movement on actin filaments toward the minus

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Description

Mutations in SLC16A2 are the cause of Allan-Herndon-Dudley syndrome

Accurate transcription initiation on TATA-containing class II genes involves the ordered assembly of RNA polymerase II (POLR2A

The protein encoded by this gene is a tumor suppressor| with lowered expression levels found in gastric| renal| colorectal| lung| and breast cancer tissues

3-dimercapto-1-propanesulfonic acid (DMPS) (By similarity)

YWHAB encodes a protein (tyrosine 3-monooxygenase/tryptophan 5-monooxygenase activation protein beta) belonging to the 14-3-3 family of proteins

MyoD Polyclonal Antibody, 100ul[BT-AP05723] 3D Culture Mutations in SLC16A2 are theMYO9B encodes a member of the myosin family of actin based molecular motor heavy chain proteins. The protein represents an unconventional myosin; it should not be confused with the conventional non muscle myosin 9 (MYH9). The protein has four IQ motifs located in the neck domain that bind calmodulin, which serves as a light chain. The protein complex has a single headed structure and exhibits processive movement on actin filaments toward the minus

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