Human IMPAD1 protein, His tag (active)

Cannot supply to this region.

SKU:: GTX67074-PRO
Additional Names:: inositol monophosphatase domain containing 1 , GPAPP , IMP 3 , IMP-3 , IMPA3
Application:: FuncS
Concentration:: 0.25 mg/ml
Physical State:: Liquid
Storage Conditions:: -20[o]C Aliquot. Avoid freeze/thaw cycles. Store undiluted., 2-8[o]C Aliquot. Avoid freeze/thaw cycles. Store undiluted., -20[o]C/-70[o]C Aliquot. Avoid freeze/thaw cycles. Store undiluted.
Supplier:: Genetex
Buffer:: PBS, no preservatives.
Immunogen:: inositol monophosphatase domain containing 1
Species:: Human
Uniprot:: Q9NX62
Synonyms:: Golgi 3-prime phosphoadenosine 5-prime phosphate 3-prime phosphatase;Golgi-resident adenosine 3',5'-bisphosphate 3'-phosphatase;golgi-resident nucleotide phosphatase;golgi-resident PAP phosphatase;GPAPP;IMP 3;IMP-3;IMPA3;IMPAD1;IMPase 3;inositol monophosphatase domain containing 1;inositol monophosphatase domain-containing protein 1;inositol-1(or 4)-monophosphatase 3;myo-inositol monophosphatase A3;phosphoadenosine phosphate 3'-nucleotidase
Extra Details:: This gene encodes a member of the inositol monophosphatase family. The encoded protein 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. [provided by RefSeq, Dec 2011]