PMPCA Antikörper
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- Target Alle PMPCA Produkte
- PMPCA (Peptidase (Mitochondrial Processing) alpha (PMPCA))
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Reaktivität
- Human, Maus, Ratte
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Wirt
- Kaninchen
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Klonalität
- Polyklonal
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Konjugat
- Dieser PMPCA Antikörper ist unkonjugiert
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Applikation
- Western Blotting (WB)
- Aufreinigung
- Affinity purification
- Immunogen
- Recombinant protein of human PMPCA
- Isotyp
- IgG
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- Applikationshinweise
- WB 1:500 - 1:2000
- Beschränkungen
- Nur für Forschungszwecke einsetzbar
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- Konzentration
- 1 mg/mL
- Buffer
- Buffer: PBS with 0.02 % sodium azide, 50 % glycerol, pH 7.3.
- Konservierungsmittel
- Sodium azide
- Vorsichtsmaßnahmen
- This product contains Sodium azide: a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.
- Lagerung
- -20 °C
- Informationen zur Lagerung
- Store at -20°C. Avoid freeze / thaw cycles.
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- Target
- PMPCA (Peptidase (Mitochondrial Processing) alpha (PMPCA))
- Andere Bezeichnung
- PMPCA (PMPCA Produkte)
- Synonyme
- Alpha-MPP antikoerper, INPP5E antikoerper, 1200002L24Rik antikoerper, 4933435E07Rik antikoerper, P-55 antikoerper, wu:fi19e06 antikoerper, wu:fj83d11 antikoerper, zgc:101647 antikoerper, MGC114896 antikoerper, DKFZp459H0315 antikoerper, peptidase, mitochondrial processing alpha subunit antikoerper, peptidase (mitochondrial processing) alpha antikoerper, peptidase (mitochondrial processing) alpha S homeolog antikoerper, PMPCA antikoerper, Pmpca antikoerper, pmpca antikoerper, pmpca.S antikoerper
- Hintergrund
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Synonyms: 1200002L24Rik,4933435E07Rik,Alpha MPP,Alpha-MPP,FLJ26258,Inositol polyphosphate 5 phosphatase, 72 kD,INPP5E,KIAA0123,MGC104197,MGC93916,Mitochondrial matrix processing protease, alpha subunit,mitochondrial processing peptidase subunit alpha,Mitochondrial-processing peptidase subunit alpha,MPPA,P 55,P-55,Peptidase (mitochondrial processing) alpha,pmpca,RP11-413M3.1,RP23-306D20.8,SCAR2
Background: The protein encoded by this gene is found in the mitochondrion, where it represents the alpha subunit of a proteolytic heterodimer. This heterodimer is responsible for cleaving the transit peptide from nuclear-encoded mitochondrial proteins. Defects in this gene are a cause of spinocerebellar ataxia, autosomal recessive 2.
- Molekulargewicht
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Observed_MW: 110kDa
Calculated_MW: 44kDa/58kDa
- Gen-ID
- 23203
- UniProt
- Q10713
- Pathways
- Inositol Metabolic Process, SARS-CoV-2 Protein Interaktom
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