IMPAD1 Protein (His tag)
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- Antigène Voir toutes IMPAD1 Protéines
- IMPAD1 (Inositol Monophosphatase Domain Containing 1 (IMPAD1))
- Type de proteíne
- Recombinant
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Origine
- Humain
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Source
- Escherichia coli (E. coli)
- Purification/Conjugué
- Cette IMPAD1 protéine est marqué à la His tag.
- Application
- SDS-PAGE (SDS)
- Pureté
- > 90 % by SDS - PAGE
- Top Product
- Discover our top product IMPAD1 Protéine
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- Commentaires
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Synonyms: Inositol monophosphatase 3, GPAPP, IMP 3, IMP-3, IMPA3
- Restrictions
- For Research Use only
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- Format
- Liquid
- Concentration
- 1 mg/ml (determined by Bradford assay)
- Buffer
- 20 mM Tris-HCl buffer (pH 8.0) containing 2 M Urea, 20% glycerol
- Stock
- 4 °C
- Stockage commentaire
- Avoid repeated freezing and thawing cycles.
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- Antigène
- IMPAD1 (Inositol Monophosphatase Domain Containing 1 (IMPAD1))
- Autre désignation
- IMPAD1 (IMPAD1 Produits)
- Synonymes
- IMP 3 Protein, RGD1306455 Protein, gPAPP Protein, impa3 Protein, 1110001C20Rik Protein, AA408880 Protein, AI451589 Protein, AL022796 Protein, B230207P20 Protein, Jaws Protein, GPAPP Protein, IMP-3 Protein, IMPA3 Protein, IMPase 3 Protein, zgc:123256 Protein, inositol monophosphatase domain containing 1 Protein, inositol monophosphatase domain containing 1 S homeolog Protein, Impad1 Protein, impad1.S Protein, IMPAD1 Protein, impad1 Protein
- Sujet
- Inositol monophosphatase 3, also known as IMPAD1, 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.
- Poids moléculaire
- 37.6kDa (349aa)
- NCBI Accession
- NP_060283
- Pathways
- Glycosaminoglycan Metabolic Process
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