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  • KD/KO Validated

AMPD1-Specific Polyklonaler Antikörper

AMPD1-Specific Polyklonal Antikörper für IHC, IP, WB, ELISA

Wirt / Isotyp

Kaninchen / IgG

Getestete Reaktivität

human, Maus, Ratte

Anwendung

WB, IP, IHC, ELISA

Konjugation

Unkonjugiert

Kat-Nr. : 19780-1-AP

Synonyme

AMP deaminase 1, AMP deaminase isoform M, AMPD1, AMPD1-Specific, MAD, MADA, Myoadenylate deaminase



Geprüfte Anwendungen

Erfolgreiche Detektion in WBMaus-Skelettmuskelgewebe
Erfolgreiche IPMaus-Skelettmuskelgewebe
Erfolgreiche Detektion in IHCMaus-Skelettmuskelgewebe
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 : 1:500-1:3000
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

19780-1-AP bindet in WB, IP, IHC, ELISA AMPD1-Specific 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 Peptid
Vollständiger Name adenosine monophosphate deaminase 1 (isoform M)
Berechnetes Molekulargewicht 87 kDa
Beobachtetes Molekulargewicht 75-83 kDa
GenBank-ZugangsnummerNM_000036
Gene symbol AMPD1
Gene ID (NCBI) 270
Konjugation Unkonjugiert
Form Liquid
Reinigungsmethode Antigen-Affinitätsreinigung
Lagerungspuffer PBS mit 0.02% Natriumazid und 50% Glycerin pH 7.3.
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

AMPD1, also named as MAD and MADA, belongs to the adenosine and AMP deaminases family. AMP deaminase plays a critical role in energy metabolism. It catalyzes the reaction: AMP + H2O = IMP + NH3. Defects in AMPD1 are the cause of adenosine monophosphate deaminase deficiency muscle type (AMPDDM) which is a metabolic disorder resulting in exercise-related myopathy. The antibody is specific to AMPD1.

Protokolle

Produktspezifische Protokolle
WB protocol for AMPD1-Specific antibody 19780-1-APProtokoll herunterladen
IHC protocol for AMPD1-Specific antibody 19780-1-APProtokoll herunterladen
IP protocol for AMPD1-Specific antibody 19780-1-APProtokoll herunterladen
Standard-Protokolle
Klicken Sie hier, um unsere Standardprotokolle anzuzeigen

Publikationen

SpeciesApplicationTitle
mouseWB

iScience

Phosphate depletion in insulin-insensitive skeletal muscle drives AMPD activation and sarcopenia in chronic kidney disease

Authors - Ana Andres-Hernando
  • KO Validated
humanIHC

Front Oncol

AMPD1 Is Associated With the Immune Response and Serves as a Prognostic Marker in HER2-Positive Breast Cancer.

Authors - Long Wang
mouseWB

Sci Adv

Lactate metabolism is essential in early-onset mitochondrial myopathy

Authors - Zhenkang Chen

Rezensionen

The reviews below have been submitted by verified Proteintech customers who received an incentive forproviding their feedback.


FH

Laila (Verified Customer) (07-22-2022)

This antibody worked great with Bovine tissue with a total of 60 ug of protein and very little non-specific binding.

  • Applications: Western Blot
  • Primary Antibody Dilution: 1:1000
  • Cell Tissue Type: bovine skeletal muscle
AMPD1-Specific Antibody Western Blot validation (1:1000 dilution) in bovine skeletal muscle (Cat no:19780-1-AP)