Methylmalonyl Coenzyme A mutase/MUT Polyklonaler Antikörper

Methylmalonyl Coenzyme A mutase/MUT Polyklonal Antikörper für WB, IHC, IP, ELISA

Wirt / Isotyp

Kaninchen / IgG

Getestete Reaktivität

human, Maus, Ratte

Anwendung

WB, IHC, IP, ELISA

Konjugation

Unkonjugiert

Publikationen(6)

Kat-Nr. : 17034-1-AP

Synonyme

MUT, EC:5.4.99.2, MCM, Methylmalonyl CoA isomerase, Methylmalonyl Coenzyme A mutase



Geprüfte Anwendungen

Erfolgreiche Detektion in WBHEK-293-Zellen, HeLa-Zellen, HepG2-Zellen
Erfolgreiche IPHepG2-Zellen
Erfolgreiche Detektion in IHChumanes Leberkarzinomgewebe, humanes Prostatakarzinomgewebe
Hinweis: Antigendemaskierung mit TE-Puffer pH 9,0 empfohlen. (*) Wahlweise kann die Antigendemaskierung auch mit Citratpuffer pH 6,0 erfolgen.

Empfohlene Verdünnung

AnwendungVerdünnung
Western Blot (WB)WB : 1:2000-1:12000
Immunpräzipitation (IP)IP : 0.5-4.0 ug for 1.0-3.0 mg of total protein lysate
Immunhistochemie (IHC)IHC : 1:50-1:500
It is recommended that this reagent should be titrated in each testing system to obtain optimal results.
Sample-dependent, check data in validation data gallery

Produktinformation

17034-1-AP bindet in WB, IHC, IP, ELISA Methylmalonyl Coenzyme A mutase/MUT und zeigt Reaktivität mit human, Maus, Ratten

Getestete Reaktivität human, Maus, Ratte
In Publikationen genannte Reaktivitäthuman, Maus
Wirt / Isotyp Kaninchen / IgG
Klonalität Polyklonal
Typ Antikörper
Immunogen Methylmalonyl Coenzyme A mutase/MUT fusion protein Ag10523
Vollständiger Name methylmalonyl Coenzyme A mutase
Berechnetes Molekulargewicht 750 aa, 83 kDa
Beobachtetes Molekulargewicht 78 kDa
GenBank-ZugangsnummerBC016282
Gene symbol MUT
Gene ID (NCBI) 4594
Konjugation Unkonjugiert
Form Liquid
Reinigungsmethode Antigen-Affinitätsreinigung
Lagerungspuffer PBS with 0.02% sodium azide and 50% glycerol
LagerungsbedingungenBei -20°C lagern. Nach dem Versand ein Jahr lang stabil Aliquotieren ist bei -20oC Lagerung nicht notwendig. 20ul Größen enthalten 0,1% BSA.

Hintergrundinformationen

Methylmalonyl Coenzyme A mutase (MUT) is an enzyme that plays a crucial role in the metabolism of certain amino acids and fatty acids (PMID: 15647267). Mutations in the MUT gene can lead to methylmalonic acidemia, a metabolic disorder characterized by the accumulation of toxic compounds such as methylmalonyl-CoA and propionyl-CoA (PMID: 30428564), resulting in life-threatening metabolic acidosis, respiratory distress, neurological impairment, hyperammonemia, and ketosis (PMID: 32679819). MUT is essential for maintaining normal metabolic processes and its dysfunction can have significant health implications, highlighting its importance in both basic metabolism and clinical medicine (PMID: 23041189).

Protokolle

PRODUKTSPEZIFISCHE PROTOKOLLE
WB protocol for Methylmalonyl Coenzyme A mutase/MUT antibody 17034-1-APProtokoll herunterladen
IHC protocol for Methylmalonyl Coenzyme A mutase/MUT antibody 17034-1-APProtokoll herunterladenl
IP protocol for Methylmalonyl Coenzyme A mutase/MUT antibody 17034-1-APProtokoll herunterladen
STANDARD-PROTOKOLLE
Klicken Sie hier, um unsere Standardprotokolle anzuzeigen

Publikationen

SpeciesApplicationTitle
mouseIHC

Hepatology

Promoterless, Nuclease-Free Genome Editing Confers a Growth Advantage for Corrected Hepatocytes in Mice With Methylmalonic Acidemia.

Authors - Randy J Chandler
mouse,humanWB

Cells

Inactivity of Peptidase ClpP Causes Primary Accumulation of Mitochondrial Disaggregase ClpX with Its Interacting Nucleoid Proteins, and of mtDNA.

Authors - Jana Key
mouseIHC

PLoS One

Novel AAV-mediated genome editing therapy improves health and survival in a mouse model of methylmalonic acidemia

Authors - Shengwen Zhang
mouseWB

EMBO Mol Med

A coordinated multiorgan metabolic response contributes to human mitochondrial myopathy

Authors - Nneka Southwell
humanWB

Biochim Biophys Acta Mol Basis Dis

ACSS3 regulates the metabolic homeostasis of epithelial cells and alleviates pulmonary fibrosis

Authors - Lan Wang
humanWB,IHC

Am J Pathol

Aging-associated Metabolite Methylmalonic Acid Increases Susceptibility to Pulmonary Fibrosis

Authors - Kai Xu
  • KD Validated