ATG7 Rabbit Polyclonal Antibody, 100ul Pipette Holder Mutation of CEBPA is associated

Mutation of CEBPA is associated with acute myeloid leukemia

which suggests the encoded protein may be a component of the 40S ribosomal subunit

PDPK1 (3-Phosphoinositide Dependent Protein Kinase 1) is a Protein Coding gene

thereby signaling their vesicular transport between membrane compartments

CAP-Gly domain containing linker protein 1 encoded by CLIP1 links endocytic vesicles to microtubules

ATG7 Rabbit Polyclonal Antibody, 100ul Pipette Holder Mutation of CEBPA is associatedThis gene encodes an E1 like activating enzyme that is essential for autophagy and cytoplasmic to vacuole transport. The encoded protein is also thought to modulate p53 dependent cell cycle pathways during prolonged metabolic stress. It has been associated with multiple functions, including axon membrane trafficking, axonal homeostasis, mitophagy, adipose differentiation, and hematopoietic stem cell maintenance. Alternative splicing results in