MMAA Antikörper
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- Target Alle MMAA Antikörper anzeigen
- MMAA (Methylmalonic Aciduria (Cobalamin Deficiency) Type A (MMAA))
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Reaktivität
- Human
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Wirt
- Maus
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Klonalität
- Monoklonal
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Konjugat
- Dieser MMAA Antikörper ist unkonjugiert
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Applikation
- Western Blotting (WB), Immunohistochemistry (IHC), Immunofluorescence (IF)
- Produktmerkmale
- Homo sapiens methylmalonic aciduria (cobalamin deficiency) cblA type (MMAA), nuclear gene encoding mitochondrial protein
- Aufreinigung
- Purified from mouse ascites fluids by affinity chromatography
- Immunogen
- Full length human recombinant protein of human MMAA (NP_785454) produced in HEK293T cell.
- Klon
- 3G5
- Isotyp
- IgG2a
- Top Product
- Discover our top product MMAA Primärantikörper
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anti-Methylmalonic Aciduria (Cobalamin Deficiency) Type A (MMAA) (AA 56-84), (N-Term) antibody
MMAA Reaktivität: Human, Maus WB, IHC (p) Wirt: Kaninchen Polyclonal RB24782 unconjugated
anti-Methylmalonic Aciduria (Cobalamin Deficiency) Type A (MMAA) (AA 1-418) antibodyMMAA Reaktivität: Human WB Wirt: Maus Polyclonal unconjugated
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- Applikationshinweise
- WB 1:2000, IHC 1:150, IF 1:100,
- Kommentare
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The concentration of the product may vary between diferrent lots.
- Beschränkungen
- Nur für Forschungszwecke einsetzbar
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- Format
- Liquid
- Konzentration
- 0.5-1.0 mg/mL
- Buffer
- PBS (PH 7.3) containing 1 % BSA, 50 % glycerol and 0.02 % sodium azide.
- 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
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- Target
- MMAA (Methylmalonic Aciduria (Cobalamin Deficiency) Type A (MMAA))
- Andere Bezeichnung
- MMAA (MMAA Produkte)
- Synonyme
- 2810018E08Rik antikoerper, AI840684 antikoerper, cblA antikoerper, methylmalonic aciduria (cobalamin deficiency) type A antikoerper, methylmalonic aciduria (cobalamin deficiency) cblA type antikoerper, Mmaa antikoerper, MMAA antikoerper
- Hintergrund
- The protein encoded by this gene is involved in the translocation of cobalamin into the mitochondrion, where it is used in the final steps of adenosylcobalamin synthesis. Adenosylcobalamin is a coenzyme required for the activity of methylmalonyl-CoA mutase. Defects in this gene are a cause of methylmalonic aciduria.
- Molekulargewicht
- 39 kDa
- Gen-ID
- 166785
- NCBI Accession
- NM_172250
- HGNC
- 166785
- Pathways
- Monocarboxylic Acid Catabolic Process
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