Rabbit Polyclonal Smac/Diablo antibody. Suitable for WB, IHC-P and reacts with Mouse, Human samples. Cited in 10 publications. Immunogen corresponding to Synthetic Peptide within Human DIABLO aa 200 to C-terminus.
View Alternative Names
SMAC, DIABLO, Diablo IAP-binding mitochondrial protein, Direct IAP-binding protein with low pI, Second mitochondria-derived activator of caspases
- IHC-P
Supplier Data
Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections) - Anti-Smac/Diablo antibody (AB8114)
Immunohistochemical analysis of paraffin-embedded human ovary tissue with ab8114 at 5 μg/mL. Sections were fixed with formaldehyde and blocked with 10% serum for 1 h at RT; antigen retrieval was by heat mediation with a citrate buffer (pH6). Samples were incubated with primary antibody overnight at 4˚C. A goat anti-rabbit IgG H&L (HRP) at 1/250 was used as secondary. Counter stained with Hematoxylin.
- WB
Supplier Data
Western blot - Anti-Smac/Diablo antibody (AB8114)
All lanes:
Western blot - Anti-Smac/Diablo antibody (ab8114) at 1 µg/mL
All lanes:
NIH3T3 cell lysate at 15 µg
Secondary
All lanes:
Goat anti-rabbit IgG HRP conjugate at 1/10000 dilution
Predicted band size: 27 kDa
false
- WB
Supplier Data
Western blot - Anti-Smac/Diablo antibody (AB8114)
All lanes : Anti-Smac / Diablo antibody (ab8114) at 1 μg/mL, 1h incubation at RT in 5% NFM/TBST.
Loading : 15 μg of lysates per lane.
Secondary : Goat anti-rabbit IgG HRP conjugate at 1/10000 dilution.
All lanes:
Western blot - Anti-Smac/Diablo antibody (ab8114)
Predicted band size: 27 kDa
false
- WB
Unknown
Western blot - Anti-Smac/Diablo antibody (AB8114)
All lanes:
Western blot - Anti-Smac/Diablo antibody (ab8114) at 1 µg/mL
Lane 1:
human heart tissue lysate with absence of blocking peptide
Lane 2:
human heart tissue lysate with Smac / Diablo peptide (<a href='/en-us/products/unavailable/smac-diablo-peptide-ab8380'>ab8380</a>)
Predicted band size: 27 kDa
Observed band size: 25 kDa
false
Reactivity data
Properties and storage information
Form
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Purification notes
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Shipped at conditions
Appropriate short-term storage duration
Appropriate short-term storage conditions
Appropriate long-term storage conditions
Aliquoting information
Storage information
Supplementary information
This supplementary information is collated from multiple sources and compiled automatically.
Biological function summary
Smac/Diablo plays a significant role in programmed cell death by binding to IAPs and negating their inhibition of caspases the key executors of apoptosis. Smac/Diablo releases from mitochondria into the cytosol when apoptotic signals activate. It does not form complexes but interacts with IAPs facilitating the activation of caspases and enhancing the apoptotic response. Its interaction with IAPs highlights its important function in apoptosis regulation.
Pathways
Smac/Diablo integrates into the mitochondrial apoptosis pathway contributing to the intrinsic pathway of apoptosis. It closely interacts with proteins such as caspases and IAPs. This integration is important for apoptosis regulation linking mitochondrial outer membrane permeabilization with the activation of caspases. Additionally the protein engages in the cytochrome c pathway promoting apoptosis by restricting IAPs and aiding in the release of cytochrome c important for apoptosis progression.
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Target data
Publications (10)
Recent publications for all applications. Explore the full list and refine your search
eLife 12: PubMed37129366
2023
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iScience 25:103715 PubMed35072007
2022
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The Journal of biological chemistry 295:3029-3039 PubMed31996372
2020
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BioMed research international 2019:2035682 PubMed31737654
2019
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Molecular biology of the cell 30:1272-1284 PubMed30893019
2019
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The American journal of Chinese medicine 47:39-61 PubMed30612456
2019
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Oncology reports 41:67-76 PubMed30365143
2018
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Frontiers in endocrinology 6:191 PubMed26834700
2016
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BMC complementary and alternative medicine 15:241 PubMed26187498
2015
Applications
WB
Species
Rat
Brain : a journal of neurology 137:2329-45 PubMed24934289
2014
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Unspecified application
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Product promise
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