IMPAD1, human recombinant

IMPAD1, human recombinant is available at Gentaur for Next week delivery.

Catalyzes the hydrolysis of phosphoadenosine phosphate (PAP) to adenosine monophosphate (AMP).

Biomolecule/Target: IMPAD1

Alternates names: Inositol monophosphatase 3, GPAPP, IMP 3, IMP-3, IMPA3

Synonyms: Inositol monophosphatase 3, GPAPP, IMP 3, IMP-3, IMPA3

Background Information: IMPAD1, also known as Inositol monophosphatase 3, is a member of the inositol monophosphatase family. IMPAD1 is localized to the Golgi apparatus and catalyzes the hydrolysis of phosphoadenosine phosphate (PAP) to adenosine monophosphate (AMP). Mutations in this gene are a cause of GRAPP type chondrodysplasia with joint dislocations, and a pseudogene of this gene is located on the long arm of chromosome 1. Recombinant human IMPAD1 protein, fused to His-tag at N-terminus, was expressed in E.coli and purified by conventional chromatography, after refolding of the isolated inclusion bodies in a renaturation buffer.

Reconstitution Instructions: N/A

NCBI Gene Symbol: IMPAD1

Gene ID: 54928

NCBI Accession: Q9NX62