MMAA anticorps (AbBy Fluor® 647)
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- Antigène Voir toutes MMAA Anticorps
- MMAA (Methylmalonic Aciduria (Cobalamin Deficiency) Type A (MMAA))
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Reactivité
- Humain, Souris, Rat
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Hôte
- Lapin
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Clonalité
- Polyclonal
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Conjugué
- Cet anticorp MMAA est conjugé à/à la AbBy Fluor® 647
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Application
- Western Blotting (WB), Immunofluorescence (Paraffin-embedded Sections) (IF (p))
- Réactivité croisée
- Humain, Souris, Rat
- Purification
- Purified by Protein A.
- Immunogène
- KLH conjugated synthetic peptide derived from human MMAA/cblA
- Isotype
- IgG
- Top Product
- Discover our top product MMAA Anticorps primaire
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- Indications d'application
- IF(IHC-P) 1:50-200
- Restrictions
- For Research Use only
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- Format
- Liquid
- Concentration
- 1 μg/μL
- Buffer
- Aqueous buffered solution containing 0.01M TBS ( pH 7.4) with 1 % BSA, 0.03 % Proclin300 and 50 % Glycerol.
- Agent conservateur
- ProClin
- Précaution d'utilisation
- This product contains ProClin: a POISONOUS AND HAZARDOUS SUBSTANCE, which should be handled by trained staff only.
- Stock
- -20 °C
- Stockage commentaire
- Store at -20°C. Aliquot into multiple vials to avoid repeated freeze-thaw cycles.
- Date de péremption
- 12 months
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- Antigène
- MMAA (Methylmalonic Aciduria (Cobalamin Deficiency) Type A (MMAA))
- Autre désignation
- cblA (MMAA Produits)
- Synonymes
- anticorps 2810018E08Rik, anticorps AI840684, anticorps cblA, anticorps methylmalonic aciduria (cobalamin deficiency) type A, anticorps methylmalonic aciduria (cobalamin deficiency) cblA type, anticorps Mmaa, anticorps MMAA
- Sujet
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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].
- ID gène
- 166785
- Pathways
- Monocarboxylic Acid Catabolic Process
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