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MEP1A Protein (AA 22-601) (His tag)
MEP1A
Origine: Humain
Hôte: Escherichia coli (E. coli)
Recombinant
> 90 % by SDS - PAGE
SDS
Active
N° du produit ABIN6387876
Détail du produit
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Antigène
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MEP1A
(Meprin A, alpha (PABA Peptide Hydrolase) (MEP1A))
Type de proteíne
Recombinant
Activité biologique
Active
Attributs du protein
AA 22-601
Origine
Toutes les origines à travers MEP1A Protéines
Humain
Source
Toutes les sources à travers MEP1A Protéines
Escherichia coli (E. coli)
Purification/Conjugué
Cette MEP1A protéine est marqué à la His tag.
Application
SDS-PAGE (SDS)
Séquence
MGSSHHHHHH SSGLVPRGSH MAAYKLVLIR HGESAWNLEN RFSGWYDADL SPAGHEEAKR GGQALRDAGY EFDICFTSVQ KRAIRTLWTV LDAIDQMWLP VVRTWRLNER HYGGLTGLNK AETAAKHGEA QVKIWRRSYD VPPPPMEPDH PFYSNISKDR RYADLTEDQL PSCESLKDTI ARALPFWNEE IVPQIKEGKR VLIAAHGNSL RGIVKHLEGL SEEAIMELNL PTGIPIVYEL DKNLKPIKPM QFLGDEETVR KAMEAVAAQG KAKK
Pureté
> 90 % by SDS - PAGE
Biological Activity Comment
Specific activity is >300 units/mg, in which One unit will convert 1.0 umole of 3-phosphoglycerate to 2-phosphoglcerate per minute at pH 7.6 at 37C.
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Information d'application
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Indications d'application
Optimal working dilution should be determined by the investigator.
Restrictions
For Research Use only
Stockage
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Format
Liquid
Concentration
1 mg/mL
Buffer
Liquid. In 20 mM Tris-HCl buffer( pH 8.0) containing 10 % glycerol, 1 mM DTT
Stock
4 °C,-20 °C,-80 °C
Stockage commentaire
Can be stored at +4C short term (1-2 weeks). For long term storage, aliquot and store at -20C or -70C. Avoid repeated freezing and thawing cycles.
Détail du antigène
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Antigène
MEP1A
(Meprin A, alpha (PABA Peptide Hydrolase) (MEP1A))
Autre désignation
MEP1A (MEP1A Produits )
Synonymes
AI098089 Protein, AW107200 Protein, Mep-1 Protein, Mep-1a Protein, Mep1 Protein, PPHA Protein, meprin A subunit alpha Protein, meprin 1 alpha Protein, Mep1a Protein, MEP1A Protein
Sujet
PGAM1 belongs to the phosphoglycerate mutase family. This protein is important components of glucose and 2,3-BPGA (2,3-bisphosphoglycerate) metabolism and catalyzes the reversible reaction of 3-phosphoglycerate (3-PGA) to 2-phosphoglycerate (2-PGA) in the glycolytic pathway. The PGAM is a dimeric enzyme containing, in different tissues, different proportions of a slow-migrating muscle (MM) isozyme, a fast-migrating brain (BB) isozyme, and a hybrid form (MB). Mutations in this protein cause muscle phosphoglycerate mutase efficiency, also known as glycogen storage disease X. Recombinant human PGAM protein, fused to His-tag at N-terminus, was expressed in E.coli and purified by using conventional chromatography techniques.
Poids moléculaire
30.9 kDa (274aa), confirmed by MALDI-TOF
NCBI Accession
NP_002620
UniProt
P18669
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