MCCC2 anticorps (Center)
Aperçu rapide pour MCCC2 anticorps (Center) (ABIN2855455)
Antigène
Voir toutes MCCC2 AnticorpsReactivité
Hôte
Clonalité
Conjugué
Application
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Épitope
- Center
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Réactivité croisée
- Rat (Rattus), Xenopus laevis, Poisson zèbre (Danio rerio), Xenopus tropicalis
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Réactivité croisée (Details)
- Rat (88 %), Xenopus laevis (84 %), Zebrafish (84 %), Xenopus tropicalis (85 %)
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Attributs du produit
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Rabbit Polyclonal antibody to MCCC2 (methylcrotonoyl-Coenzyme A carboxylase 2 (beta))
MCCC2 antibody [N1C1] -
Purification
- Purified by antigen-affinity chromatography.
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Immunogène
- Recombinant protein encompassing a sequence within the center region of human MCCC2. The exact sequence is proprietary.
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Isotype
- IgG
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Indications d'application
- Suggested dilution Reference IHC (Formalin-fixed paraffin-embedded sections) 1:100-1:1000* Western blot 1:500-1:3000* Not tested in other applications. *Optimal dilutions/concentrations should be determined by the researcher.Suggested dilutionReferenceIHC (Formalin-fixed paraffin-embedded sections)1:100-1:1000* Western blot1:500-1:3000*
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Commentaires
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Positive Control: 293T , A431 , H1299 , HepG2 , mouse liver
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Restrictions
- For Research Use only
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Format
- Liquid
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Concentration
- 1 mg/mL
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Buffer
- 0.1M Tris, 0.1M Glycine, 10 % Glycerol ( pH 7). 0.01 % Thimerosal was added as a preservative.
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Agent conservateur
- Thimerosal (Merthiolate)
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Précaution d'utilisation
- This product contains Thimerosal (Merthiolate): a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.
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Stock
- -20 °C
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Stockage commentaire
- Keep as concentrated solution. Aliquot and store at -20°C or below. Avoid multiple freeze-thaw cycles.
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- MCCC2 (Methylcrotonoyl-CoA Carboxylase 2 (Beta) (MCCC2))
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Autre désignation
- MCCC2
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Sujet
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This gene encodes the small subunit of 3-methylcrotonyl-CoA carboxylase. This enzyme functions as a heterodimer and catalyzes the carboxylation of 3-methylcrotonyl-CoA to form 3-methylglutaconyl-CoA. Mutations in this gene are associated with 3-Methylcrotonylglycinuria, an autosomal recessive disorder of leucine catabolism.
Cellular Localization: Mitochondrion matrix -
Poids moléculaire
- 61 kDa
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ID gène
- 64087
Antigène
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