MMAA anticorps (N-Term)

N° du produit ABIN5538833

Détail du produit anti-MMAA anticorps

Antigène: MMAA (Methylmalonic Aciduria (Cobalamin Deficiency) Type A (MMAA))

Épitope: AA 56-84, N-Term

Reactivité: Humain, Souris

Hôte: Lapin

Clonalité: Polyclonal

Conjugué: Cet anticorp MMAA est non-conjugé

Application: Western Blotting (WB), Immunohistochemistry (Paraffin-embedded Sections) (IHC (p))

Purification: This antibody is purified through a protein A column, followed by peptide affinity purification.

Immunogène: This MMAA antibody is generated from rabbits immunized with a KLH conjugated synthetic peptide between 56-84 amino acids from the N-terminal region of human MMAA.

Isotype: Ig Fraction

Information d'application

Indications d'application: For WB starting dilution is: 1:500

For IHC-P starting dilution is: 1:50~100

Restrictions: For Research Use only

Stockage

Format: Liquid

Buffer: Supplied in PBS with 0.09 % (W/V) 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: 4 °C,-20 °C

Stockage commentaire: Store at 4°C for three months and -20°C, stable for up to one year. As with all antibodies care should be taken to avoid repeated freeze thaw cycles. Antibodies should not be exposed to prolonged high temperatures.

Détails sur MMAA

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: 47 kDa

ID gène: 166785

UniProt: Q8IVH4

Pathways: Monocarboxylic Acid Catabolic Process