TNNI3 anticorps (AA 41-49)

N° du produit ABIN363301

Cet anticorps Souris Monoclonal détecte spécifiquement TNNI3 dans WB, ELISA, IHC, IP et FACS. Il présente une réactivité envers Humain, Souris et Rat.

Aperçu rapide pour TNNI3 anticorps (AA 41-49) (ABIN363301)

Antigène: TNNI3 (Cardiac Troponin I (TNNI3))

Reactivité: Humain, Souris, Rat

Hôte: Souris

Clonalité: Monoclonal

Conjugué: Cet anticorp TNNI3 est non-conjugé

Application: Western Blotting (WB), ELISA, Immunohistochemistry (IHC), Immunoprecipitation (IP), Flow Cytometry (FACS)

Clone: 19C7

Détail du produit anti-TNNI3 anticorps

Épitope: AA 41-49

Specificité: Reacts with protein from Human, Mouse, Rat, Bovine, Canine, Feline, Fish, Goat, Porcine and Rabbit

Réactivité croisée (Details): Equally reactive with free cardiac troponin I (cTnI) and cTnI forming complexes with other troponin components. (In the presence of 5 mM EDTA). Antibodies are not affected by heparin, phosphorylation, oxidation and troponin complex formation. No cross-reaction with skeletal muscle troponin I.

Purification: Purified (protein A)

Immunogène: Native troponin complex, (epitope 41-49 aa)

Isotype: IgG2b

Information d'application

Indications d'application:

Working dilution: Optimal dilution should be determined by the end user.
The following are guidelines only :
WB1:100-1:2000 IHC1:10-1:500 IP1:10-1:500 Sandwich ELISA1:100-1:2000

Restrictions: For Research Use only

Stockage

Format: Liquid

Concentration: 3.2 mg/mL

Buffer: PBS, ( pH 7.4), Sodium azide 0.1 %

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: Short term storage at +4°C. For extended periods store in aliquots at -20°C. Antibodies are guaranteed for 6 month from date of receipt.

Date de péremption: 6 months

Détails sur TNNI3

Antigène: TNNI3 (Cardiac Troponin I (TNNI3))

Autre désignation: Troponin I, Cardiac Muscle

Sujet: Belongs to the troponin I family. Defects in TNNI3 are the cause of familial hypertrophic cardiomyopathy type 7 (CMH7), familial restrictive cardiomyopathy type 1 (RCM1), cardiomyopathy dilated type 2A (CMD2A) and cardiomyopathy dilated type 1FF (CMD1FF).

UniProt: P19429