GFPT1 / Unconjugated /
Product Details
| Description | Controls the flux of glucose into the hexosamine pathway. Most likely involved in regulating the availability of precursors for N- and O-linked glycosylation of proteins. Regulates the circadian expression of clock genes ARNTL/BMAL1 and CRY1. Defects in GFPT1 are the cause of limb-girdle myasthenia with tubular aggregates (LGMTA). A congenital myasthenic syndrome characterized by onset of proximal muscle weakness in the first decade. | |
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| Conjugate | Unconjugated | |
| Clone | ||
| Target Species | Human, Monkey, Rat | |
| Applications | FC, ICC, WB | |
| Supplier | HuaBio | |
| Catalog # | Sign in to view product details, citations, and spectra | |
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About GFPT1
This gene encodes the first and rate-limiting enzyme of the hexosamine pathway and controls the flux of glucose into the hexosamine pathway. The product of this gene catalyzes the formation of glucosamine 6-phosphate. [provided by RefSeq, Sep 2008]
This gene encodes the first and rate-limiting enzyme of the hexosamine pathway and controls the flux of glucose into the hexosamine pathway. The product of this gene catalyzes the formation of glucosamine 6-phosphate. [provided by RefSeq, Sep 2008]
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171 GFPT1 antibodies from over 14 suppliers available with over 39 conjugates.
