IMPAD1 Polyclonal Antibody

Rs. 16,500.00
SKU E-AB-13332

Overview

Synonyms 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
Swissprot Q9NX62
Source Rabbit
Reactivity Human,Mouse,Rat
Immunogen Synthetic peptide of human IMPAD1
Application IHC,ELISA
Recommended dilution IHC 1:25-1:100
Concentration 1.4mg/mL
Clonality Polyclonal

Properties

Cellular localization  
Tissue specificity  
Isotype IgG
Purification Affinity purification
Conjugation Unconjugated
Storage instructions Store at -20℃. Avoid freeze / thaw cycles.
Storage buffer PBS with 0.05% sodium azide, 50% glycerol, PH7.3
Background 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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