MMAA anticorps (N-Term)

N° du produit ABIN2789699

Détail du produit anti-MMAA anticorps

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

Épitope: N-Term

Reactivité: Humain, Rat, Boeuf (Vache), Chien, Cobaye, Cheval, Lapin

Hôte: Lapin

Clonalité: Polyclonal

Conjugué: Cet anticorp MMAA est non-conjugé

Application: Western Blotting (WB)

Séquence: GQRACLAEAI TLVESTHSRK KELAQVLLQK VLLYHREQEQ SNKGKPLAFR

Homologie: Cow: 85%, Dog: 86%, Guinea Pig: 92%, Horse: 86%, Human: 100%, Rabbit: 93%, Rat: 92%

Attributs du produit: This is a rabbit polyclonal antibody against MMAA. It was validated on Western Blot.

Purification: Affinity Purified

Information d'application

Indications d'application: Optimal working dilutions should be determined experimentally by the investigator.

Commentaires:

Antigen size: 418 AA

Restrictions: For Research Use only

Stockage

Format: Liquid

Concentration: Lot specific

Buffer: Liquid. Purified antibody supplied in 1x PBS buffer with 0.09 % (w/v) sodium azide and 2 % sucrose.

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.

Conseil sur la manipulation: Avoid repeated freeze-thaw cycles.

Stock: -20 °C

Stockage commentaire: For short term use, store at 2-8°C up to 1 week. For long term storage, store at -20°C in small aliquots to prevent freeze-thaw cycles.

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.
Alias Symbols: MGC120010, MGC120011, MGC120012, MGC120013, cblA
Protein Interaction Partner: MMAA, MUT,
Protein Size: 418

Poids moléculaire: 46 kDa

ID gène: 166785

NCBI Accession: NM_172250, NP_758454

UniProt: Q8IVH4

Pathways: Monocarboxylic Acid Catabolic Process