Datenblatt

Biologische Beschreibung

Spezifität	PAN TEAD Antibody [A12P9] weist endogene Spiegel des gesamten Pan-TEAD-Proteins nach.
Hintergrund	Die TEAD-Familie von Transkriptionsfaktoren, bestehend aus TEAD1, TEAD2, TEAD3 und TEAD4, ist eine konservierte Gruppe von DNA-bindenden Proteinen, die Gene regulieren, die Zellproliferation, Differenzierung, Überleben, Apoptose, Gewebewachstum und Regeneration steuern. Sie wirken als zentrale nachgeschaltete Effektoren des Hippo-Signalwegs und integrieren mechanische und biochemische Inputs, um die Gewebehomöostase aufrechtzuerhalten und die Organgröße zu kontrollieren. Alle TEAD-Proteine teilen eine N-terminale TEA-DNA-bindende Domäne (~70–75 Aminosäuren) mit einer Helix-Turn-Helix-Faltung, die MCAT-Elemente in Zielpromotoren erkennt, und eine C-terminale YAP-bindende Domäne (YBD) mit einer Immunglobulin-ähnlichen Faltung, die die transkriptionellen Coaktivatoren YAP und TAZ rekrutiert. Diese Coaktivatoren sind essentiell für eine robuste transkriptionelle Aktivierung von Zielgenen wie CTGF und CYR61, da TEADs allein eine geringe intrinsische Aktivität aufweisen. Die koordinierte TEAD-Funktion beeinflusst die Zytoskelettdynamik, die Wundheilung und die Geweberegeneration. Die Dysregulation eines TEAD-Familienmitglieds, oft durch aberrante YAP/TAZ-Aktivierung, treibt onkogene transkriptionelle Programme an, fördert die Metastasierung und ist mit Entwicklungsstörungen, fibroproliferativen Erkrankungen und Kardiomyopathien verbunden.

Spezifität

PAN TEAD Antibody [A12P9] weist endogene Spiegel des gesamten Pan-TEAD-Proteins nach.

Hintergrund

Die TEAD-Familie von Transkriptionsfaktoren, bestehend aus TEAD1, TEAD2, TEAD3 und TEAD4, ist eine konservierte Gruppe von DNA-bindenden Proteinen, die Gene regulieren, die Zellproliferation, Differenzierung, Überleben, Apoptose, Gewebewachstum und Regeneration steuern. Sie wirken als zentrale nachgeschaltete Effektoren des Hippo-Signalwegs und integrieren mechanische und biochemische Inputs, um die Gewebehomöostase aufrechtzuerhalten und die Organgröße zu kontrollieren. Alle TEAD-Proteine teilen eine N-terminale TEA-DNA-bindende Domäne (~70–75 Aminosäuren) mit einer Helix-Turn-Helix-Faltung, die MCAT-Elemente in Zielpromotoren erkennt, und eine C-terminale YAP-bindende Domäne (YBD) mit einer Immunglobulin-ähnlichen Faltung, die die transkriptionellen Coaktivatoren YAP und TAZ rekrutiert. Diese Coaktivatoren sind essentiell für eine robuste transkriptionelle Aktivierung von Zielgenen wie CTGF und CYR61, da TEADs allein eine geringe intrinsische Aktivität aufweisen. Die koordinierte TEAD-Funktion beeinflusst die Zytoskelettdynamik, die Wundheilung und die Geweberegeneration. Die Dysregulation eines TEAD-Familienmitglieds, oft durch aberrante YAP/TAZ-Aktivierung, treibt onkogene transkriptionelle Programme an, fördert die Metastasierung und ist mit Entwicklungsstörungen, fibroproliferativen Erkrankungen und Kardiomyopathien verbunden.

Nutzungsinformationen

Anwendung

WB

Verdünnung

WB

1:1000

Reaktivität

Human

Quelle

Rabbit Monoclonal Antibody

MW

48 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/Nuclear Lysis Buffer (containing Protease Inhibitor Cocktail)，and homogenize the tissue at a low temperature. 2. Adherent cell: Aspirate the culture medium and wash the cells with ice-cold PBS twice. Lyse the cells by adding an appropriate volume of RIPA/Nuclear Lysis Buffer (containing Protease Inhibitor Cocktail) and put the sample on ice for 5 min. 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. Lyse the cells by adding an appropriate volume of RIPA/Nuclear Lysis Buffer (containing Protease Inhibitor Cocktail) and put the sample on ice for 5 min. 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 1. 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/Nuclear Lysis Buffer (containing Protease Inhibitor Cocktail)，and homogenize the tissue at a low temperature.

2. Adherent cell: Aspirate the culture medium and wash the cells with ice-cold PBS twice. Lyse the cells by adding an appropriate volume of RIPA/Nuclear Lysis Buffer (containing Protease Inhibitor Cocktail) and put the sample on ice for 5 min.

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. Lyse the cells by adding an appropriate volume of RIPA/Nuclear Lysis Buffer (containing Protease Inhibitor Cocktail) and put the sample on ice for 5 min.

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

1. 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/18579750/
https://pubmed.ncbi.nlm.nih.gov/20123908/

Anwendungsdaten

WB

Validiert von Selleck

Lane 1: HeLa, Lane 2: SW480