PDSS2 anticorps (Biotin)

N° du produit ABIN1388671

Cet anticorps Lapin Polyclonal détecte spécifiquement PDSS2 dans ELISA, IHC (p) et IHC (fro). Il présente une réactivité envers Chien.

Aperçu rapide pour PDSS2 anticorps (Biotin) (ABIN1388671)

Antigène: PDSS2 (Prenyl (Decaprenyl) Diphosphate Synthase, Subunit 2 (PDSS2))

Reactivité: Chien

Hôte: Lapin

Clonalité: Polyclonal

Conjugué: Cet anticorp PDSS2 est conjugé à/à la Biotin

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

Détail du produit anti-PDSS2 anticorps (Biotin)

Homologie: Dog,Pig,Horse,Rabbit

Purification: Purified by Protein A.

Immunogène: KLH conjugated synthetic peptide derived from dog PDSS2

Isotype: IgG

Information d'application

Indications d'application: WB 1:100-1000
IHC-P 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: Sodium azide

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

Stock: -20 °C

Stockage commentaire: Store at -20°C for 12 months.

Date de péremption: 12 months

Détails sur PDSS2

Antigène: PDSS2 (Prenyl (Decaprenyl) Diphosphate Synthase, Subunit 2 (PDSS2))

Autre désignation: PDSS2

Sujet:

Synonyms: ll-trans-decaprenyl-diphosphate synthase subunit 2, bA59I9.3, C6orf210, Candidate tumor suppressor protein, chromosome 6 open reading frame 210, Decaprenyl pyrophosphate synthase subunit 2, decaprenyl pyrophosphate synthetase subunit 2, Decaprenyl-diphosphate synthase subunit 2, DLP1, DLP1_HUMAN, hDLP1, Pdss2, prenyl decaprenyl diphosphate synthase, subunit 2, subunit 2 of decaprenyl diphosphate synthase.

Background: The protein encoded by this gene is an enzyme that synthesizes the prenyl side-chain of coenzyme Q, or ubiquinone, one of the key elements in the respiratory chain. The gene product catalyzes the formation of all trans-polyprenyl pyrophosphates from isopentyl diphosphate in the assembly of polyisoprenoid side chains, the first step in coenzyme Q biosynthesis. Defects in this gene are a cause of coenzyme Q10 deficiency.