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MP17L Rabbit Polyclonal Antibody, 50ul Organelle Studies Defects in CLCN7 are the
MP17L Rabbit Polyclonal Antibody, 50ul Organelle Studies Defects in CLCN7 are the
MP17L Rabbit Polyclonal Antibody, 50ul Organelle Studies Defects in CLCN7 are the
MP17L Rabbit Polyclonal Antibody, 50ul Organelle Studies Defects in CLCN7 are the

MP17L Rabbit Polyclonal Antibody, 50ul Organelle Studies Defects in CLCN7 are the

SKU: 3540982391

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MP17L Rabbit Polyclonal Antibody, 50ul Organelle Studies Defects in CLCN7 are the

Store: ecoilumi.com.br · Domain: ecoilumi.com.br

Description

Defects in CLCN7 are the cause of osteopetrosis autosomal recessive type 4 (OPTB4)

but also as a potent signalling molecule

This gene exhibits elevated expression levels in multiple human cancers

Mouse studies suggest that this gene may serve as a functional substitute for the dystrophin gene and therefore

Required for the fusion of plasma membranes and early endosomes

MP17L Rabbit Polyclonal Antibody, 50ul Organelle Studies Defects in CLCN7 are the

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