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AB231289

Anti-Cleaved Caspase-3 antibody [EPR21032] - BSA and Azide free

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(2 Publications)

Rabbit Recombinant Monoclonal Caspase-3 antibody. Carrier free. Suitable for WB and reacts with Mouse samples. Cited in 2 publications.

View Alternative Names

Cpp32, Casp3, Caspase-3, CASP-3, Apopain, Cysteine protease CPP32, LICE, Protein Yama, SREBP cleavage activity 1, CPP-32, SCA-1

1 Images
Western blot - Anti-Cleaved Caspase-3 antibody [EPR21032] - BSA and Azide free (AB231289)
  • WB

Supplier Data

Western blot - Anti-Cleaved Caspase-3 antibody [EPR21032] - BSA and Azide free (AB231289)

Blocking and dilution buffer : 5% NFDM/TBST.

Observed molecular masses are consistent with the literature for full-length and cleaved caspase 3 (PMID : 9922454, PMID 16221205).

This data was developed using the same antibody clone in a different buffer formulation containing PBS, BSA, glycerol, and sodium azide (ab214430).

All lanes:

Western blot - Anti-Cleaved Caspase-3 antibody [EPR21032] (<a href='/en-us/products/primary-antibodies/cleaved-caspase-3-antibody-epr21032-ab214430'>ab214430</a>) at 1/5000 dilution

Lane 1:

Untreated NIH/3T3 (mouse embryo fibroblast cell line) whole cell lysate at 10 µg

Lane 2:

NIH/3T3 cells treated with 1 uM staurosprine for 4 hours, whole cell lysate at 10 µg

Secondary

All lanes:

Western blot - Goat Anti-Rabbit IgG H&L (HRP) (<a href='/en-us/products/secondary-antibodies/goat-rabbit-igg-h-l-hrp-ab97051'>ab97051</a>) at 1/100000 dilution

Predicted band size: 32 kDa

Observed band size: 14 kDa,17 kDa,19 kDa,24 kDa,29 kDa,32 kDa

true

Exposure time: 3min

Key facts

Host species

Rabbit

Clonality

Monoclonal

Clone number

EPR21032

Isotype

IgG

Carrier free

Yes

Reacts with

Mouse

Applications

WB

applications

Immunogen

The exact immunogen used to generate this antibody is proprietary information.

Specificity

ab214430 recognises both pro-Caspase-3 and p17 cleavage fragments.

Reactivity data

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Product details

ab231289 is the carrier-free version of ab214430.

Conjugation ready
Our carrier-free antibodies are typically supplied in a PBS-only formulation, purified and free of BSA, sodium azide and glycerol. This conjugation-ready format is designed for use with fluorochromes, metal isotopes, oligonucleotides, and enzymes, which makes them ideal for antibody labelling, functional and cell-based assays, flow-based assays (e.g. mass cytometry) and Multiplex Imaging applications.

Use our conjugation kits for antibody conjugates that are ready-to-use in as little as 20 minutes with 1 minute hands-on-time and 100% antibody recovery: available for fluorescent dyes, HRP, biotin and gold.

Compatibility
This product is compatible with the Maxpar® Antibody Labeling Kit from Fluidigm, without the need for antibody preparation. Maxpar® is a trademark of Fluidigm Canada Inc.

Properties and storage information

Form
Liquid
Purification technique
Affinity purification Protein A
Storage buffer
pH: 7.2 - 7.4 Constituents: PBS
Shipped at conditions
Blue Ice
Appropriate short-term storage conditions
+4°C
Appropriate long-term storage conditions
+4°C
Storage information
Do Not Freeze

Supplementary information

This supplementary information is collated from multiple sources and compiled automatically.

The Cleaved Caspase-3 also known as active caspase 3 plays an important role in the execution phase of cell apoptosis. The caspase 3 molecule has a molecular weight of approximately 32 kDa. It undergoes cleavage into subunits that are important for its activation marking its conversion into the cleaved form. Cleaved caspase is widely expressed in various tissues with a notable presence in the cytoplasm of cells undergoing apoptotic processes. Cleavage of caspase 3 results in the formation of a functional enzyme that participates in the degradation of cellular components during apoptosis.
Biological function summary

Caspase 3 acts as an executioner enzyme in the process of programmed cell death. Its cleavage from the inactive zymogen form into the active form triggers apoptotic pathways ensuring the removal of damaged or unnecessary cells. Cleaved caspase operates within a proteolytic cascade often in conjunction with other caspases such as caspase 9. Once activated caspase 3 targets and cleaves specific cellular substrates contributing to the characteristic morphological changes and DNA fragmentation associated with apoptosis.

Pathways

Cleaved caspase 3 is significant within the intrinsic and extrinsic apoptotic pathways. It acts downstream of initiator caspases such as caspase 9 in the intrinsic pathway where its activation involves mitochondrial signals. In the extrinsic pathway it closely associates with caspase 8 mediating cell death signals from extracellular triggers. These pathways ensure that cleaved caspase 3 fulfills its role as a critical mediator of apoptosis linking upstream death signals to cellular dismantling during the apoptosis process.

Cleaved caspase 3 connects to conditions such as cancer and neurodegenerative diseases. In cancer dysregulation of caspase 3 activity may lead to evasion of apoptosis facilitating tumor progression. Therapeutic approaches aim to restore its apoptotic functions in cancer cells. In neurodegenerative diseases like Alzheimer's disease abnormal activation of cleaved caspase 3 contributes to neuronal loss. It interacts with proteins like amyloid precursor protein promoting the pathological changes associated with this disorder. Understanding these interactions provides insights into potential therapeutic avenues.

Product protocols

For this product, it's our understanding that no specific protocols are required. You can visit:

Target data

Thiol protease that acts as a major effector caspase involved in the execution phase of apoptosis (PubMed : 16469926, PubMed : 8934524). Following cleavage and activation by initiator caspases (CASP8, CASP9 and/or CASP10), mediates execution of apoptosis by catalyzing cleavage of many proteins (PubMed : 16469926, PubMed : 8934524). At the onset of apoptosis, it proteolytically cleaves poly(ADP-ribose) polymerase PARP1 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 (CASP6, CASP7 and CASP9, respectively). Cleaves and inactivates interleukin-18 (IL18) (By similarity). Triggers cell adhesion in sympathetic neurons through RET cleavage (By similarity). Cleaves IL-1 beta between an Asp and an Ala, releasing the mature cytokine which is involved in a variety of inflammatory processes (By similarity). Cleaves and inhibits serine/threonine-protein kinase AKT1 in response to oxidative stress (PubMed : 12124386). Acts as an inhibitor of type I interferon production during virus-induced apoptosis by mediating cleavage of antiviral proteins CGAS, IRF3 and MAVS, thereby preventing cytokine overproduction (PubMed : 30878284). Also involved in pyroptosis by mediating cleavage and activation of gasdermin-E (GSDME) (By similarity). Cleaves XRCC4 and phospholipid scramblase proteins XKR4, XKR8 and XKR9, leading to promote phosphatidylserine exposure on apoptotic cell surface (PubMed : 25231987, PubMed : 33725486). Cleaves BIRC6 following inhibition of BIRC6-caspase binding by DIABLO/SMAC (By similarity).
See full target information Casp3

Publications (2)

Recent publications for all applications. Explore the full list and refine your search

Aging 15:1859-1877 PubMed36988541

2023

P53/miR-34a/SIRT1 positive feedback loop regulates the termination of liver regeneration.

Applications

Unspecified application

Species

Unspecified reactive species

Junhua Gong,Minghua Cong,Hao Wu,Menghao Wang,He Bai,Jingyuan Wang,Keting Que,Kaiwen Zheng,Wenfeng Zhang,Xiaoli Yang,Jianping Gong,Hanping Shi,Mingyong Miao,Fangchao Yuan

Neuropsychiatric disease and treatment 17:1667-1678 PubMed34079264

2021

LncRNA GAS5 Silencing Attenuates Oxygen-Glucose Deprivation/Reperfusion-Induced Injury in Brain Microvascular Endothelial Cells via miR-34b-3p-Dependent Regulation of EPHA4.

Applications

Unspecified application

Species

Unspecified reactive species

Bin Shen,Lan Wang,Yuejun Xu,Hongwei Wang,Shiyi He
View all publications

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