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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

4.1
USD162.00 USD190.00

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

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Description

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

but also as a potent signalling molecule

This gene encodes an enzyme belonging to the diacylglycerol acyltransferase family

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

ACTB encodes one of six different actin proteins

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

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