| Full Name | inositol monophosphatase domain containing 1 |
| 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. [provided by RefSeq, Dec 2011] |
| Synonyms | IMP3 Antibody , IMPA3 Antibody , IMP 3 Antibody , IMPAD1 Antibody , GPAPP Antibody |
| Host | Rabbit |
| Clonality | Polyclonal |
| Isotype | IgG |
| Immunogen | A synthetic peptide corresponding to an Internal region of Human IMPAD1 |
| Antigen Species | Human |
| Species Reactivity | Human |
| Predict Reactivity Note | Cow: 93%; Dog: 93%; Guinea Pig: 93%; Horse: 93%; Human: 100%; Mouse: 100%; Rabbit: 100%; Rat: 100% |
| Conjugation | Unconjugated |