Datenblatt

Biologische Beschreibung

Spezifität	UBE3A Antibody [P7K8] erkennt endogene Spiegel des gesamten UBE3A-Proteins.
Hintergrund	UBE3A, auch bekannt als E6AP (E6 Associated Protein), ist eine E3-Ubiquitinligase und das erste identifizierte Mitglied der HECT-Familie (Homologous to the E6 Carboxyl Terminus) der E3-Ligasen. Es ist gekennzeichnet durch eine hochkonservierte C-terminale katalytische Domäne, die aus 350 Resten besteht. Veränderungen der E6AP-Funktion, ob durch Aktivierung oder Verlust, sind mit verschiedenen menschlichen Krankheiten verbunden. Der Verlust der E6AP-Funktion aufgrund von Deletion, Prägungsdefekten oder Mutationen im UBE3A-Gen, das in der Chromosomenregion 15q11–13 liegt, ist mit dem Angelman-Syndrom, einer neurologischen Störung, assoziiert. Die meisten der natürlichen Mutationen in UBE3A führen zu Deletionen, die verkürzte Formen von E6AP erzeugen, denen die vollständige HECT-Domäne fehlt. Etwa 10 % der genetischen Veränderungen sind jedoch Punktmutationen innerhalb der E6AP-kodierenden Region. Umgekehrt wurde die Duplikation des UBE3A-Gens als ein beitragender Faktor in einigen Fällen von Autismus-Spektrum-Störung vorgeschlagen. Das onkogene E6-Protein von Hochrisiko-Humanen Papillomviren (HPV16 und HPV18) kann UBE3A kapern, was zu einer unsachgemäßen Ubiquitinierung spezifischer zellulärer Proteine, insbesondere p53, führt, was im Zusammenhang mit der Krebsentwicklung von Bedeutung ist. In Neuronen führt die Störung der UBE3A-Funktion zu einer erhöhten Arc-Expression und einer Reduktion der AMPA-Rezeptoren (AMPARs) an exzitatorischen Synapsen, was potenziell zu den neurologischen Symptomen des Angelman-Syndroms beitragen kann.

Spezifität

UBE3A Antibody [P7K8] erkennt endogene Spiegel des gesamten UBE3A-Proteins.

Hintergrund

UBE3A, auch bekannt als E6AP (E6 Associated Protein), ist eine E3-Ubiquitinligase und das erste identifizierte Mitglied der HECT-Familie (Homologous to the E6 Carboxyl Terminus) der E3-Ligasen. Es ist gekennzeichnet durch eine hochkonservierte C-terminale katalytische Domäne, die aus 350 Resten besteht. Veränderungen der E6AP-Funktion, ob durch Aktivierung oder Verlust, sind mit verschiedenen menschlichen Krankheiten verbunden. Der Verlust der E6AP-Funktion aufgrund von Deletion, Prägungsdefekten oder Mutationen im UBE3A-Gen, das in der Chromosomenregion 15q11–13 liegt, ist mit dem Angelman-Syndrom, einer neurologischen Störung, assoziiert. Die meisten der natürlichen Mutationen in UBE3A führen zu Deletionen, die verkürzte Formen von E6AP erzeugen, denen die vollständige HECT-Domäne fehlt. Etwa 10 % der genetischen Veränderungen sind jedoch Punktmutationen innerhalb der E6AP-kodierenden Region. Umgekehrt wurde die Duplikation des UBE3A-Gens als ein beitragender Faktor in einigen Fällen von Autismus-Spektrum-Störung vorgeschlagen. Das onkogene E6-Protein von Hochrisiko-Humanen Papillomviren (HPV16 und HPV18) kann UBE3A kapern, was zu einer unsachgemäßen Ubiquitinierung spezifischer zellulärer Proteine, insbesondere p53, führt, was im Zusammenhang mit der Krebsentwicklung von Bedeutung ist. In Neuronen führt die Störung der UBE3A-Funktion zu einer erhöhten Arc-Expression und einer Reduktion der AMPA-Rezeptoren (AMPARs) an exzitatorischen Synapsen, was potenziell zu den neurologischen Symptomen des Angelman-Syndroms beitragen kann.

Nutzungsinformationen

Anwendung

WB

Verdünnung

WB

1:1000

Reaktivität

Human, Mouse, Rat, Monkey

Quelle

Rabbit Monoclonal Antibody

MW

98 kDa

Lagerpuffer

PBS, pH 7.2+50% Glycerol+0.05% BSA+0.01% NaN₃

Lagerung
(Ab dem Datum des Erhalts)

–20°C (avoid freeze-thaw cycles), 2 years

Experimentelle Methoden
WB	Experimental Protocol: Sample preparation 1. Tissue: Lyse the tissue sample by adding an appropriate volume of ice-cold RIPA/NP-40 Lysis Buffer (containing Protease Inhibitor Cocktail)，and homogenize the tissue at a low temperature or lyse it by sonication on ice, then incubate on ice for 30 minutes. 2. Adherent cell: Aspirate the culture medium and transfer the cells into an EP tube. Wash the cells with ice-cold PBS twice. Add an appropriate volume of RIPA/NP-40 Lysis Buffer (containing Protease Inhibitor Cocktail), sonicate to lyse the cells, and incubate on ice for 30 minutes. 3. Suspension cell: Transfer the culture medium to a pre-cooled centrifuge tube. Centrifuge and aspirate the supernatant. Wash the cells with ice-cold PBS twice.Add an appropriate volume of RIPA/NP-40 Lysis Buffer (containing Protease Inhibitor Cocktail), sonicate to lyse the cells, and incubate on ice for 30 minutes. 4. Place the lysate into a pre-cooled microcentrifuge tube. Centrifuge at 4°C for 15 min. Collect the supernatant; 5. Remove a small volume of lysate to determine the protein concentration; 6. Combine the lysate with protein loading buffer. Boil 20 µL sample under 95-100°C for 5 min. Centrifuge for 5 min after cool down on ice. Electrophoretic separation 1. According to the concentration of extracted protein, load appropriate amount of protein sample and marker onto SDS-PAGE gels for electrophoresis. Recommended separating gel (lower gel) concentration: 10%. Reference Table for Selecting SDS-PAGE Separation Gel Concentrations 2. Power up 80V for 30 minutes. Then the power supply is adjusted (110 V~150 V), the Marker is observed, and the electrophoresis can be stopped when the indicator band of the predyed protein Marker where the protein is located is properly separated. (Note that the current should not be too large when electrophoresis, too large current (more than 150 mA) will cause the temperature to rise, affecting the result of running glue. If high currents cannot be avoided, an ice bath can be used to cool the bath.) Transfer membrane 1. Take out the converter, soak the clip and consumables in the pre-cooled converter; 2. Activate PVDF membrane with methanol for 1 min and rinse with transfer buffer; 3. Install it in the order of "black edge of clip - sponge - filter paper - filter paper - glue -PVDF membrane - filter paper - filter paper - sponge - white edge of clip"; 4. The protein was electrotransferred to PVDF membrane. ( 0.45 µm PVDF membrane is recommended ) Reference Table for Selecting PVDF Membrane Pore Size Specifications Recommended conditions for wet transfer: 200 mA, 120 min. ( Note that the transfer conditions can be adjusted according to the protein size. For high-molecular-weight proteins, a higher current and longer transfer time are recommended. However, ensure that the transfer tank remains at a low temperature to prevent gel melting.) Block 1. After electrotransfer, wash the film with TBST at room temperature for 5 minutes; 2. Incubate the film in the blocking solution for 1 hour at room temperature; 3. Wash the film with TBST for 3 times, 5 minutes each time. Antibody incubation 1. Use 5% skim milk powder to prepare the primary antibody working liquid (recommended dilution ratio for primary antibody 1:1000), gently shake and incubate with the film at 4°C overnight; 2. Wash the film with TBST 3 times, 5 minutes each time; 3. Add the secondary antibody to the blocking solution and incubate with the film gently at room temperature for 1 hour; 4. After incubation, wash the film with TBST 3 times for 5 minutes each time. Antibody staining 965. Add the prepared ECL luminescent substrate (or select other color developing substrate according to the second antibody) and mix evenly; 2. Incubate with the film for 1 minute, remove excess substrate (keep the film moist), wrap with plastic film, and expose in the imaging system.

Experimentelle Methoden

WB

Experimental Protocol:

Sample preparation

1. Tissue: Lyse the tissue sample by adding an appropriate volume of ice-cold RIPA/NP-40 Lysis Buffer (containing Protease Inhibitor Cocktail)，and homogenize the tissue at a low temperature or lyse it by sonication on ice, then incubate on ice for 30 minutes.

2. Adherent cell: Aspirate the culture medium and transfer the cells into an EP tube. Wash the cells with ice-cold PBS twice. Add an appropriate volume of RIPA/NP-40 Lysis Buffer (containing Protease Inhibitor Cocktail), sonicate to lyse the cells, and incubate on ice for 30 minutes.

3. Suspension cell: Transfer the culture medium to a pre-cooled centrifuge tube. Centrifuge and aspirate the supernatant. Wash the cells with ice-cold PBS twice.Add an appropriate volume of RIPA/NP-40 Lysis Buffer (containing Protease Inhibitor Cocktail), sonicate to lyse the cells, and incubate on ice for 30 minutes.

4. Place the lysate into a pre-cooled microcentrifuge tube. Centrifuge at 4°C for 15 min. Collect the supernatant;

5. Remove a small volume of lysate to determine the protein concentration;

6. Combine the lysate with protein loading buffer. Boil 20 µL sample under 95-100°C for 5 min. Centrifuge for 5 min after cool down on ice.

Electrophoretic separation

1. According to the concentration of extracted protein, load appropriate amount of protein sample and marker onto SDS-PAGE gels for electrophoresis. Recommended separating gel (lower gel) concentration: 10%. Reference Table for Selecting SDS-PAGE Separation Gel Concentrations

2. Power up 80V for 30 minutes. Then the power supply is adjusted (110 V~150 V), the Marker is observed, and the electrophoresis can be stopped when the indicator band of the predyed protein Marker where the protein is located is properly separated. (Note that the current should not be too large when electrophoresis, too large current (more than 150 mA) will cause the temperature to rise, affecting the result of running glue. If high currents cannot be avoided, an ice bath can be used to cool the bath.)

Transfer membrane

1. Take out the converter, soak the clip and consumables in the pre-cooled converter;

2. Activate PVDF membrane with methanol for 1 min and rinse with transfer buffer;

3. Install it in the order of "black edge of clip - sponge - filter paper - filter paper - glue -PVDF membrane - filter paper - filter paper - sponge - white edge of clip";

4. The protein was electrotransferred to PVDF membrane. ( 0.45 µm PVDF membrane is recommended ) Reference Table for Selecting PVDF Membrane Pore Size Specifications

Recommended conditions for wet transfer: 200 mA, 120 min.

( Note that the transfer conditions can be adjusted according to the protein size. For high-molecular-weight proteins, a higher current and longer transfer time are recommended. However, ensure that the transfer tank remains at a low temperature to prevent gel melting.)

Block

1. After electrotransfer, wash the film with TBST at room temperature for 5 minutes;

2. Incubate the film in the blocking solution for 1 hour at room temperature;

3. Wash the film with TBST for 3 times, 5 minutes each time.

Antibody incubation

1. Use 5% skim milk powder to prepare the primary antibody working liquid (recommended dilution ratio for primary antibody 1:1000), gently shake and incubate with the film at 4°C overnight;

2. Wash the film with TBST 3 times, 5 minutes each time;

3. Add the secondary antibody to the blocking solution and incubate with the film gently at room temperature for 1 hour;

4. After incubation, wash the film with TBST 3 times for 5 minutes each time.

Antibody staining

965. Add the prepared ECL luminescent substrate (or select other color developing substrate according to the second antibody) and mix evenly;

2. Incubate with the film for 1 minute, remove excess substrate (keep the film moist), wrap with plastic film, and expose in the imaging system.

Referenzen

https://pubmed.ncbi.nlm.nih.gov/24273172/
https://pubmed.ncbi.nlm.nih.gov/8380895/

Anwendungsdaten

WB

Validiert von Selleck

Lane 1: K562
Lane 2: NIH/3T3
Lane 3: COS-7
Lane 4: A172