GAA Antikörper (AA 70-225)
Kurzübersicht für GAA Antikörper (AA 70-225) (ABIN7444157)
Target
Alle GAA Antikörper anzeigenReaktivität
Wirt
Klonalität
Konjugat
Applikation
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Bindungsspezifität
- AA 70-225
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Verwendungszweck
- Polyclonal Antibody to Glucosidase Alpha, Acid (GaA)
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Spezifität
- The antibody is a rabbit polyclonal antibody raised against GaA. It has been selected for its ability to recognize GaA in immunohistochemical staining and western blotting.
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Kreuzreaktivität
- Maus
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Aufreinigung
- Antigen-specific affinity chromatography followed by Protein A affinity chromatography
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Immunogen
- Recombinant Glucosidase Alpha, Acid (GaA) corresdonding to Glu70~Lys225
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Isotyp
- IgG
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Applikationshinweise
- Western blotting: 0.5-2 μg/mL,Immunocytochemistry in formalin fixed cells: 5-20 μg/mL,Immunohistochemistry in formalin fixed frozen section: 5-20 μg/mL,Immunohistochemistry in paraffin section: 5-20 μg/mL,Enzyme-linked Immunosorbent Assay: 0.05-2 μg/mL,Optimal working dilutions must be determined by end user.
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Kommentare
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The thermal stability is described by the loss rate. The loss rate was determined by accelerated thermal degradation test, that is, incubate the protein at 37°C for 48h, and no obvious degradation and precipitation were observed. The loss rate is less than 5% within the expiration date under appropriate storage condition.
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Beschränkungen
- Nur für Forschungszwecke einsetzbar
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Format
- Liquid
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Konzentration
- 500 μg/mL
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Buffer
- 0.01M PBS, pH 7.4, containing 0.05 % Proclin-300, 50 % glycerol.
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Konservierungsmittel
- ProClin
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Vorsichtsmaßnahmen
- This product contains ProClin: a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.
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Lagerung
- 4 °C,-20 °C
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Informationen zur Lagerung
- Store at 4°C for frequent use. Stored at -20°C in a manual defrost freezer for two year without detectable loss of activity. Avoid repeated freeze-thaw cycles.
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Haltbarkeit
- 24 months
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- GAA (Glucosidase, Alpha, Acid (GAA))
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Andere Bezeichnung
- Glucosidase Alpha, Acid
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Hintergrund
- LYAG, Acid Alpha-Glucosidase, Lysosomal Alpha-Glucosidase, Pompe Disease Glycogen Storage Disease Type II, Acid Maltase, Aglucosidase Alfa
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UniProt
- Q6P7A9
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Pathways
- Cellular Glucan Metabolic Process
Target
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