MMAA anticorps
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- Antigène Voir toutes MMAA Anticorps
- MMAA (Methylmalonic Aciduria (Cobalamin Deficiency) Type A (MMAA))
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Reactivité
- Humain
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Hôte
- Souris
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Clonalité
- Monoclonal
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Conjugué
- Cet anticorp MMAA est non-conjugé
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Application
- Western Blotting (WB), Immunohistochemistry (IHC), Immunofluorescence (IF)
- Attributs du produit
- Homo sapiens methylmalonic aciduria (cobalamin deficiency) cblA type (MMAA), nuclear gene encoding mitochondrial protein
- Purification
- Purified from mouse ascites fluids by affinity chromatography
- Immunogène
- Full length human recombinant protein of human MMAA (NP_785454) produced in HEK293T cell.
- Clone
- 3G5
- Isotype
- IgG2a
- Top Product
- Discover our top product MMAA Anticorps primaire
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anti-Methylmalonic Aciduria (Cobalamin Deficiency) Type A (MMAA) (AA 56-84), (N-Term) antibody
MMAA Reactivité: Humain, Souris WB, IHC (p) Hôte: Lapin Polyclonal RB24782 unconjugated
anti-Methylmalonic Aciduria (Cobalamin Deficiency) Type A (MMAA) (AA 1-418) antibodyMMAA Reactivité: Humain WB Hôte: Souris Polyclonal unconjugated
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- Indications d'application
- WB 1:2000, IHC 1:150, IF 1:100,
- Commentaires
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The concentration of the product may vary between diferrent lots.
- Restrictions
- For Research Use only
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- Format
- Liquid
- Concentration
- 0.5-1.0 mg/mL
- Buffer
- PBS (PH 7.3) containing 1 % BSA, 50 % glycerol and 0.02 % sodium azide.
- Agent conservateur
- Sodium azide
- Précaution d'utilisation
- This product contains sodium azide: a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.
- Stock
- -20 °C
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- Antigène
- MMAA (Methylmalonic Aciduria (Cobalamin Deficiency) Type A (MMAA))
- Autre désignation
- MMAA (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
- 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.
- Poids moléculaire
- 39 kDa
- ID gène
- 166785
- NCBI Accession
- NM_172250
- HGNC
- 166785
- Pathways
- Monocarboxylic Acid Catabolic Process
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