AMPD1 anticorps (AA 140-190)

N° du produit ABIN372277

Cet anticorps Lapin Polyclonal détecte spécifiquement AMPD1 dans WB et IHC (p). Il présente une réactivité envers Humain, Souris, Rat, Boeuf (Vache), Chien, Chimpanzé, Singe et Poisson zèbre (Danio rerio).

Aperçu rapide pour AMPD1 anticorps (AA 140-190) (ABIN372277)

Antigène: AMPD1 (Adenosine Monophosphate Deaminase 1 (AMPD1))

Reactivité: Humain, Souris, Rat, Boeuf (Vache), Chien, Chimpanzé, Singe, Poisson zèbre (Danio rerio)

Hôte: Lapin

Clonalité: Polyclonal

Conjugué: Cet anticorp AMPD1 est non-conjugé

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

Détail du produit anti-AMPD1 anticorps

Épitope: AA 140-190

Specificité: This antibody recognizes AMPD1.

Réactivité croisée (Details): Species reactivity (expected):Bovine, Chimpanzee, Dog (Canine), Monkey, Mouse, Rat and Zebrafish.
Species reactivity (tested):Human.

Purification: Immunoaffinity Chromatography.

Immunogène: Synthetic peptide corresponding to a portion of the amino acids 140-190 of Human AMPD1.

Isotype: IgG

Information d'application

Indications d'application: Immunohistochemistry on Paraffin Sections: 10 μg/mL. Western Blot: 0.5-2.0 μg/mL.
Other applications not tested.
Optimal dilutions are dependent on conditions and should be determined by the user.

Restrictions: For Research Use only

Stockage

Concentration: 0.5 mg/mL

Buffer: PBS containing 0.05 % Sodium Azide as preservative and 0.2 % Gelatin as stabilizer.

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 freezing and thawing.

Stock: 4 °C/-20 °C

Stockage commentaire: Store the antibody undiluted at 2-8 °C for one month or (in aliquots) at-20 °C for longer.

Détails sur AMPD1

Antigène: AMPD1 (Adenosine Monophosphate Deaminase 1 (AMPD1))

Autre désignation: AMP Deaminase 1 / AMPD1

Sujet: AMP deaminase (AMPD) is an allosteric enzyme that plays a critical role in energy metabolism. There are three functional isoforms of AMPD. AMPD1 is the skeletal muscle-specific isoform M located in type II muscle fibers, neuromuscular junctions and in capillaries. Defects in AMPD1 are the cause of adenosine monophosphate deaminase deficiency muscle type (AMPDDM). AMPDDM is a metabolic disorder resulting in exercise-related myopathy. It is characterized by exercise-induced muscle aches, cramps, and early fatigue.Synonyms: AMP deaminase isoform M, Myoadenylate deaminase

Poids moléculaire: 87 kDa.

ID gène: 270

NCBI Accession: NP_000027

UniProt: P23109