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CT072 Rabbit Polyclonal Antibody, 100ul Rotator Defects in this gene are

SKU: 46109128103

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CT072 Rabbit Polyclonal Antibody, 100ul Rotator Defects in this gene are

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Description

Defects in this gene are a cause of xeroderma pigmentosum complementation group F (XP-F)

This gene has been linked to both genetic and acquired hypertension

A sulfated form of cholecystokinin-8 may modulate neuronal activity in the brain

Lysosomal microenvironment has been implicated in the regulation of antigen loading into MHC II molecules

and thus induce the nuclear production of NF-kappaB

CT072 Rabbit Polyclonal Antibody, 100ul Rotator Defects in this gene are

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