GLA Antikörper (N-Term)
Kurzübersicht für GLA Antikörper (N-Term) (ABIN634024)
Target
Alle GLA Antikörper anzeigenReaktivität
Wirt
Klonalität
Konjugat
Applikation
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                                            Bindungsspezifität
- N-Term
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                                            Spezifität
- GLA antibody was raised against the N terminal of GLA
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                                            Aufreinigung
- Affinity purified
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                                            Immunogen
- GLA antibody was raised using the N terminal of GLA corresponding to a region with amino acids PQRFPHGIRQLANYVHSKGLKLGIYADVGNKTCAGFPGSFGYYDIDAQTF
 
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                                            Applikationshinweise
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                        WB: 1 µg/mL
 Optimal conditions should be determined by the investigator.
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                                            Kommentare
- 
                        GLA Blocking Peptide, (ABIN5613778), is also available for use as a blocking control in assays to test for specificity of this GLA antibody 
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                                            Beschränkungen
- Nur für Forschungszwecke einsetzbar
 
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    - 
                                            Format
- Lyophilized
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                                            Rekonstitution
- Lyophilized powder. Add distilled water for a 1 mg/mL concentration of GLA antibody in PBS
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                                            Konzentration
- Lot specific
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                                            Buffer
- PBS
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                                            Handhabung
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                        Avoid repeated freeze/thaw cycles. 
 Dilute only prior to immediate use.
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                                            Lagerung
- 4 °C/-20 °C
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                                            Informationen zur Lagerung
- Store at 2-8 °C for short periods. For longer periods of storage, store at -20 °C.
 
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    - GLA (Galactosidase, alpha (GLA))
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                                            Andere Bezeichnung
- GLA
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                                            Hintergrund
- GLA is a homodimeric glycoprotein that hydrolyses the terminal alpha-galactosyl moieties from glycolipids and glycoproteins. This enzyme predominantly hydrolyzes ceramide trihexoside, and it can catalyze the hydrolysis of melibiose into galactose and glucose. A variety of mutations in this gene affect the synthesis, processing, and stability of this enzyme, which causes Fabry disease, a rare lysosomal storage disorder that results from a failure to catabolize alpha-D-galactosyl glycolipid moieties.
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                                            Molekulargewicht
- 45 kDa (MW of target protein)
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                                            Pathways
- SARS-CoV-2 Protein Interaktom
 Target
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