MMAA Antikörper (Biotin)
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- Target Alle MMAA Antikörper anzeigen
- MMAA (Methylmalonic Aciduria (Cobalamin Deficiency) Type A (MMAA))
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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 MMAA Antikörper ist konjugiert mit Biotin
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Applikation
- Western Blotting (WB), Immunohistochemistry (Paraffin-embedded Sections) (IHC (p))
- Kreuzreaktivität
- Human, Maus, Ratte
- Aufreinigung
- Purified by Protein A.
- Immunogen
- KLH conjugated synthetic peptide derived from human MMAA/cblA
- Isotyp
- IgG
- Top Product
- Discover our top product MMAA Primärantikörper
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- Applikationshinweise
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WB 1:300-5000
IHC-P 1:200-400 - Beschränkungen
- Nur für Forschungszwecke einsetzbar
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- Format
- Liquid
- Konzentration
- 1 μg/μL
- Buffer
- Aqueous buffered solution containing 0.01M TBS ( pH 7.4) with 1 % BSA, 0.03 % Proclin300 and 50 % Glycerol.
- Konservierungsmittel
- ProClin
- Vorsichtsmaßnahmen
- This product contains ProClin: a POISONOUS AND HAZARDOUS SUBSTANCE, which should be handled by trained staff only.
- Lagerung
- -20 °C
- Informationen zur Lagerung
- Store at -20°C for 12 months.
- Haltbarkeit
- 12 months
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- Target
- MMAA (Methylmalonic Aciduria (Cobalamin Deficiency) Type A (MMAA))
- Andere Bezeichnung
- cblA (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
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Synonyms: mitochondrial, cblA, MMAA protein, Methylmalonic aciduria cobalamin deficiency cblA type, Methylmalonic aciduria cobalamin deficiency type A, Methylmalonic aciduria type A protein, Methylmalonic aciduria type A protein mitochondrial, MMAA, MMAA_HUMAN.
Background: 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. [provided by RefSeq, Jul 2008].
- Gen-ID
- 166785
- Pathways
- Monocarboxylic Acid Catabolic Process
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