Cytochrome b5 (CYTB5) (AA 9-80) anticorps (HRP)

N° du produit ABIN709910

L’anticorps Lapin Polyclonal anti- a été validé pour WB, ELISA, IHC (p) et IHC (fro). Il convient pour détecter dans des échantillons de Souris.

Aperçu rapide pour Cytochrome b5 (CYTB5) (AA 9-80) anticorps (HRP) (ABIN709910)

Antigène: Cytochrome b5 (CYTB5)

Reactivité: Souris

Hôte: Lapin

Clonalité: Polyclonal

Conjugué: HRP

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

Détail du produit

Épitope: AA 9-80

Réactivité croisée: Souris

Homologie: Human,Rat,Dog,Cow,Sheep,Pig

Purification: Purified by Protein A.

Immunogène: KLH conjugated synthetic peptide derived from human Cytochrome b5

Isotype: IgG

Information d'application

Indications d'application: WB 1:300-5000
IHC-P 1:200-400
IHC-F 1:100-500

Restrictions: For Research Use only

Stockage

Format: Liquid

Concentration: 1 μg/μL

Buffer: Aqueous buffered solution containing 0.01M TBS ( pH 7.4) with 1 % BSA, 0.03 % 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.

Conseil sur la manipulation: Do NOT add Sodium Azide! Use of Sodium Azide will inhibit enzyme activity of horseradish peroxidase.

Stock: -20 °C

Stockage commentaire: Store at -20°C. Aliquot into multiple vials to avoid repeated freeze-thaw cycles.

Date de péremption: 12 months

Détail du antigène

Antigène: Cytochrome b5 (CYTB5)

Autre désignation: Cytochrome b5

Sujet:

Synonyms: CYB 5, CYB 5A, CYB5, CYB5_HUMAN, CYB5A, Cytochrome b 5, Cytochrome b5 microsomal, Cytochrome b5, Cytochrome b5 type A microsomal, Cytochrome b5 type A, MCB 5, MCB5, Microsomal cytochrome b5, Microsomal cytochrome b5 type A, Type 1 cyt b5, CYB5A.

Background: The protein encoded by this gene is a membrane-bound cytochrome that reduces ferric hemoglobin (methemoglobin) to ferrous hemoglobin, which is required for stearyl-CoA-desaturase activity. Defects in this gene are a cause of type IV hereditary methemoglobinemia. Three transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Jun 2010]

ID gène: 1528