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Prenyl (Decaprenyl) Diphosphate Synthase, Subunit 1 (PDSS1) Peptide
PDSS1
Reactivité: Mammifères
Hôte: Synthetic
BP, WB, IHC
Aperçu rapide pour Prenyl (Decaprenyl) Diphosphate Synthase, Subunit 1 (PDSS1) Peptide (ABIN938611)
Antigène
PDSS1
(Prenyl (Decaprenyl) Diphosphate Synthase, Subunit 1 (PDSS1))
Origine
Mammifères
Source
Toutes les hôtes sur PDSS1 Peptides
Synthetic
Application
Blocking Peptide (BP), Western Blotting (WB), Immunohistochemistry (IHC)
Détail du produit
(cache)
Type de proteíne
Synthetic
Séquence
GEFLQLGSKE NENERFAHYL EKTFKKTASL IANSCKAVSV LGCPDPVVHE
Attributs du produit
A synthetic peptide for use as a blocking control in assays to test for specificity of PDSS1 antibody, Alternative Names: PDSS1 control peptide, PDSS1 antibody Blocking Peptide, Anti-PDSS1 Blocking Peptide, Prenyl decaprenyl diphosphate synthase subunit 1 Blocking Peptide, Decaprenyl Diphosphate Synthase Subunit 1 Blocking Peptide, COQ1 Blocking Peptide, MGC70953 Blocking Peptide, RP.3 Blocking Peptide, TPRT Blocking Peptide, TPT Blocking Peptide, hDPS1 Blocking Peptide, PDSS1, PDSS-1, PDSS 1, PDSS-1 Blocking Peptide, PDSS 1 Blocking Peptide
Alternatives
(show)
Information d'application
(cache)
Indications d'application
Optimal conditions should be determined by the investigator
Restrictions
For Research Use only
Stockage
(cache)
Format
Lyophilized
Reconstitution
Add 100 µL of distilled water for a final peptide concentration is 1 mg/mL.
Buffer
PBS
Conseil sur la manipulation
Avoid repeated freeze/thaw cycles.
Stock
-20 °C
Stockage commentaire
Store at -20 °C long term.
Détail du antigène
(cache)
Antigène
PDSS1
(Prenyl (Decaprenyl) Diphosphate Synthase, Subunit 1 (PDSS1))
Sujet
PDSS1 is an enzyme that elongates the prenyl side-chain of coenzyme Q, or ubiquinone, one of the key elements in the respiratory chain. PDSS1 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. The protein may be peripherally associated with the inner mitochondrial membrane, though no transit peptide has been definitively identified to date. Defects in PDSS1 gene are a cause of coenzyme Q10 deficiency.
Poids moléculaire
46 kDa
Vus récemment
(cache)
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