Caspase 3 p17 (Cleaved-Asp175) Antikörper
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- Target
- Caspase 3 p17
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Bindungsspezifität
- Cleaved-Asp175
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Reaktivität
- Human, Maus, Ratte
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Wirt
- Kaninchen
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Klonalität
- Polyklonal
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Konjugat
- Unkonjugiert
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Applikation
- Western Blotting (WB), ELISA, Immunofluorescence (IF), Immunohistochemistry (Paraffin-embedded Sections) (IHC (p))
- Produktmerkmale
- Polyclonal Antibody
- Aufreinigung
- Affinity purification
- Immunogen
- Synthesized peptide derived from the Internal region of human Caspase-3 p17
- Isotyp
- IgG
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- Applikationshinweise
- WB 1:500-2000, IHC 1:50-300, IF 1:50-300
- Beschränkungen
- Nur für Forschungszwecke einsetzbar
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- by
- Prof. Merighi, Laboratory of Neurobiology, Department of Veterinary Sciences, University of Turin
- No.
- #104629
- Datum
- 15.03.2025
- Antigen
- Caspase 3 p17
- Chargennummer
- DX03VBDV9989
- Validierte Anwendung
- Immunohistochemistry
- Positivkontrolle
The expression of caspase 3 at P5 was already attested in our laboratory (Lossi et al., 2004).
- Negativkontrolle
A control slice was processed for each experimental procedure, omitting the primary antibody.
- Bewertung
- Reference: Lossi L., Tamagno I. and Merighi A. (2004) “Molecular morphology of neuronal apoptosis: analysis of Caspase 3 activation during postnatal development of mouse cerebellar cortex.” J Mol Histol, 35(6):621-9.
- Primärantikörper
- ABIN7251013
- Sekundärantikörper
- anti-rabbit Alexa Fluor 488 (Invitrogen. Lot 2541675)
- Full Protocol
- Sample analyzed: mouse cerebellum at post-natal day (P) 5–6.
- Paraffin-embedded slices (7 µm thick) were deparaffinized and rehydrated through a graded series of alcohols and distilled water (dH2O).
- Sections were blocked in ovalbumin 1% 1 hour at room temperature.
- Antigen retrieval was performed in all the sections by microwave treatment (1 minute at 750 W + 1 minute at 250 W in citrate buffer pH 6).
- 3×5 minutes washing in 0.01 M PBS.
- Sections were incubated with the primary antibody at the following dilutions of 1:50/1:100/1:200, overnight at room temperature (primary antibody was diluted in PLL/BSA/PBS diluent).
- 3×5 minutes washing in 0.01 M PBS.
- Incubation with the anti-rabbit secondary antibody 1:400 in PLL/BSA/PBS diluent, 1 hour at room temperature.
- 3×5 minutes washing in 0.01 M PBS.
- Nuclear counterstaining was performed with DAPI 1 µg/mL, 2 minutes.
- 2×5 minutes washing in 0.01 M PBS.
- Specimens were then mounted in Fluoroshield mounting medium (Sigma).
- Anmerkungen
Passed. The antibody works in IHC-P at concentrations from 1:50-1:200
Validierung #104629 (Immunohistochemistry)ValidierungsbilderExpression of cleaved caspase 3 (cCASP3) in P6 mouse cerebellum. An immunoreactive Purkinje neuron (left) and two cCASP3-positive granule cells (right) after immunostaining with ABIN7251013 and nuclear counterstaining with 4′,6-Diamidine-2′-phenylindole dihydrochloride (DAPI). EGL = external granular layer of the cerebellar cortex; IGL = internal granular layer of the cerebellar cortex.
Protokoll -
- Format
- Liquid
- Konzentration
- 1 mg/mL
- Buffer
- PBS with 0.02 % sodium azide, 0.5 % BSA and 50 % glycerol, pH 7.4
- Konservierungsmittel
- Sodium azide
- Vorsichtsmaßnahmen
- This product contains Sodium azide: a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.
- Lagerung
- -20 °C
- Informationen zur Lagerung
- Store at -20°C. Avoid freeze / thaw cycles.
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- Target
- Caspase 3 p17
- Andere Bezeichnung
- CASP3 p17
- Hintergrund
- Involved in the activation cascade of caspases responsible for apoptosis execution. At the onset of apoptosis it proteolytically cleaves poly(ADP-ribose) polymerase (PARP) at a '216-Asp-Gly-217' bond. Cleaves and activates sterol regulatory element binding proteins (SREBPs) between the basic helix-loop-helix leucine zipper domain and the membrane attachment domain. Cleaves and activates caspase-6, -7 and -9. Involved in the cleavage of huntingtin.
- Molekulargewicht
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Observed_MW: 20 kDa
Calculated_MW: 32 kDa
- UniProt
- P42574
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