GAA Protein (AA 761-919) (His tag)
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- Antigène Voir toutes GAA Protéines
- GAA (Glucosidase, Alpha, Acid (GAA))
- Type de proteíne
- Recombinant
- Attributs du protein
- AA 761-919
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Origine
- Humain
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Source
- Escherichia coli (E. coli)
- Purification/Conjugué
- Cette GAA protéine est marqué à la His tag.
- Application
- Western Blotting (WB), SDS-PAGE (SDS), Immunogen (Imm), Positive Control (PC)
- Séquence
- Ala761-Asn919
- Attributs du produit
- Location of tag(s): N-terminal
- Pureté
- > 95 %
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Glucosidase, Alpha, Acid (GAA) (AA 204-952) protein (His tag)Crystallography grade GAA Origine: Humain Hôte: Cellules d'insectes Recombinant >95 % as determined by SDS PAGE, Size Exclusion Chromatography and Western Blot. WB, SDS, ELISA, Crys
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Glucosidase, Alpha, Acid (GAA) (AA 70-953) protein (His tag)Crystallography grade GAA Origine: Souris Hôte: Cellules d'insectes Recombinant >95 % as determined by SDS PAGE, Size Exclusion Chromatography and Western Blot. WB, SDS, ELISA, Crys
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- Indications d'application
- Optimal working dilution should be determined by the investigator.
- Commentaires
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Isoelectric Point:5.4
- Restrictions
- For Research Use only
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- Format
- Lyophilized
- Reconstitution
- Reconstitute in sterile PBS, pH 7.2 - pH 7.4.
- Buffer
- PBS, pH 7.4, containing 0.01 % SKL, 1 mM DTT, 5 % Trehalose and Proclin300.
- Agent conservateur
- ProClin
- Conseil sur la manipulation
- Avoid repeated freeze/thaw cycles
- Stock
- 4 °C,-80 °C
- Stockage commentaire
- Store at 2-8°C for one month. Aliquot and store at -80°C for 12 months.
- Date de péremption
- 12 months
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- Antigène
- GAA (Glucosidase, Alpha, Acid (GAA))
- Autre désignation
- Glucosidase Alpha, Acid (GAA Produits)
- Synonymes
- LYAG Protein, E430018M07Rik Protein, glucosidase alpha, acid Protein, glucosidase, alpha, acid Protein, transmembrane and coiled-coil domain family 1 Protein, glucosidase, alpha; acid (Pompe disease, glycogen storage disease type II) Protein, GAA Protein, Gaa Protein, TMCC1 Protein, gaa Protein
- Sujet
- LYAG, Acid Alpha-Glucosidase, Lysosomal Alpha-Glucosidase, Pompe Disease Glycogen Storage Disease Type II, Acid Maltase, Aglucosidase Alfa
- Poids moléculaire
- 18.5 kDa
- UniProt
- P10253
- Pathways
- Cellular Glucan Metabolic Process
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