Catalase anticorps

N° du produit ABIN7090817

Cet anticorps anti-Catalase est un anticorps Souris Monoclonal détectant Catalase dans WB et IHC (p). Adapté pour Humain.

Aperçu rapide pour Catalase anticorps (ABIN7090817)

Antigène: Catalase (CAT)

Reactivité: Humain

Hôte: Souris

Clonalité: Monoclonal

Conjugué: Cet anticorp Catalase est non-conjugé

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

Clone: A5A6

Détail du produit anti-Catalase anticorps

Réactivité croisée: Humain

Homologie: Mouse,Rat

Purification: Purified by Protein G.

Immunogène: KLH conjugated synthetic peptide derived from human Catalase

Isotype: IgG1, kappa

Information d'application

Indications d'application: WB 1:300-5000
IHC-P 1:200-400

Restrictions: For Research Use only

Stockage

Concentration: 1 mg/mL

Buffer: 0.01M TBS( pH 7.4) with 1 % BSA, 0.02 % Proclin300 and 50 % Glycerol.

Agent conservateur: ProClin

Précaution d'utilisation: This product contains ProClin: a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.

Stock: 4 °C,-20 °C

Stockage commentaire: Shipped at 4°C. Store at -20°C for one year. Avoid repeated freeze/thaw cycles.

Date de péremption: 12 months

Détails sur Catalase

Antigène: Catalase (CAT)

Autre désignation: Catalase

Sujet:

Synonyms: Cas1, CAT, Cs1, MGC138422, MGC138424, CATA_HUMAN.

Background: This gene encodes catalase, a key antioxidant enzyme in the bodies defense against oxidative stress. Catalase is a heme enzyme that is present in the peroxisome of nearly all aerobic cells. Catalase converts the reactive oxygen species hydrogen peroxide to water and oxygen and thereby mitigates the toxic effects of hydrogen peroxide. Oxidative stress is hypothesized to play a role in the development of many chronic or late-onset diseases such as diabetes, asthma, Alzheimer's disease, systemic lupus erythematosus, rheumatoid arthritis, and cancers. Polymorphisms in this gene have been associated with decreases in catalase activity but, to date, acatalasemia is the only disease known to be caused by this gene. [provided by RefSeq, Oct 2009]

ID gène: 847

UniProt: P04040

Pathways: Cellular Glucan Metabolic Process, Cell RedoxHomeostasis, Photoperiodism