Anti-Human/Mouse/Rat IMPAD1 Polyclonal Antibody

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.
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Properties

Data Sheet Click for Datasheet
Catalog Number PA10185
Size 100μl
Host Type Rabbit
Immunogen Synthetic peptide of human IMPAD1
Specificity
Isotype IgG
Reacitivity Human,Mouse,Rat
Clone
Uniprot Q9NX62
Concentration 1.4 mg/mL
Dilution IHC 1:25-1:100
Formulation
Application IHC,ELISA
Other Names Golgi 3 prime phosphoadenosine 5 prime phosphate 3 prime phosphatase,Golgi 3-prime phosphoadenosine 5-prime phosphate 3-prime phosphatase,Golgi resident PAP phosphatase,Golgi-resident PAP phosphatase,gPAPP,IMP 3,IMPA3,IMPA3,Impad1,IMPase 3,Inositol 1(or 4) monophosphatase 3,Inositol monophosphatase 3,Inositol monophosphatase domain containing protein 1,Inositol monophosphatase domain-containing protein 1,Inositol-1(or 4)-monophosphatase 3,Myo inositol monophosphatase A3,Myo-inositol monophosphatase A3
Storage Lyophilized product: 5 years at 2 - 8°C; Solution: 2 years at -20°C.
Postscript For research use only, not for use in diagnostic procedures.

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