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AB216263

Anti-Intron-encoded endonuclease I-SceI antibody

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(3 Publications)

Rabbit Polyclonal Intron-encoded endonuclease I-SceI antibody. Suitable for WB, ICC/IF and reacts with Saccharomyces cerevisiae samples. Cited in 3 publications. Immunogen corresponding to Recombinant Full Length Protein corresponding to Saccharomyces cerevisiae S288C SCEI.

View Alternative Names

OMEGA, SECY, Q0160, SCEI, Intron-encoded endonuclease I-SceI, 21S rRNA intron maturase, Homing endonuclease omega

2 Images
Immunocytochemistry/ Immunofluorescence - Anti-Intron-encoded endonuclease I-SceI antibody (AB216263)
  • ICC/IF

Supplier Data

Immunocytochemistry/ Immunofluorescence - Anti-Intron-encoded endonuclease I-SceI antibody (AB216263)

Immunofluorescent analysis U2OS cells transfected with GFP-SCE1 (Green) labeling SCE1 using ab216263 at 1/600 dilution (red). DAPI staining is showed and the merge figure too

Western blot - Anti-Intron-encoded endonuclease I-SceI antibody (AB216263)
  • WB

Supplier Data

Western blot - Anti-Intron-encoded endonuclease I-SceI antibody (AB216263)

All lanes:

Western blot - Anti-Intron-encoded endonuclease I-SceI antibody (ab216263) at 1/2000 dilution

Lane 1:

Non-transfected 293T cells lysate at 40 µg

Lane 2:

293T cells transfected with GFP-SCE1 lysate at 40 µg

Predicted band size: 18 kDa

false

Key facts

Host species

Rabbit

Clonality

Polyclonal

Isotype

IgG

Carrier free

No

Reacts with

Saccharomyces cerevisiae

Applications

ICC/IF, WB

applications

Immunogen

Recombinant Full Length Protein corresponding to Saccharomyces cerevisiae S288C SCEI.

P03882

Reactivity data

{ "title": "Reactivity Data", "filters": { "stats": ["", "Species", "Dilution Info", "Notes"], "tabs": { "all-applications": {"fullname" : "All Applications", "shortname": "All Applications"}, "WB" : {"fullname" : "Western blot", "shortname":"WB"}, "ICCIF" : {"fullname" : "Immunocytochemistry/ Immunofluorescence", "shortname":"ICC/IF"} }, "product-promise": { "all": "all", "testedAndGuaranteed": "tested", "guaranteed": "expected", "predicted": "predicted", "notRecommended": "not-recommended" } }, "values": { "Saccharomyces cerevisiae": { "WB-species-checked": "testedAndGuaranteed", "WB-species-dilution-info": "", "WB-species-notes": "<p></p>", "ICCIF-species-checked": "testedAndGuaranteed", "ICCIF-species-dilution-info": "", "ICCIF-species-notes": "<p></p>" } } }

Properties and storage information

Form
Liquid
Purity
Whole antiserum
Storage buffer
Preservative: 0.05% Sodium azide
Shipped at conditions
Blue Ice
Appropriate short-term storage duration
1-2 weeks
Appropriate short-term storage conditions
+4°C
Appropriate long-term storage conditions
-20°C
Aliquoting information
Upon delivery aliquot
Storage information
Avoid freeze / thaw cycle

Supplementary information

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

Intron-encoded endonuclease I-SceI also known as endonuclease I-SceI or I-SceI endonuclease is a precise and highly specific endonuclease. It recognizes and cleaves an 18-base pair sequence. This sequence is rare resulting in the enzyme being used as a molecular tool for genome editing. I-SceI is encoded by a group I intron within the mitochondrial DNA of yeast and possesses a molecular mass of approximately 30 kDa. The enzyme expression is primarily observed in eukaryotic organisms often associated with mitochondrial genetic material.
Biological function summary

I-SceI facilitates homologous recombination and DNA repair by introducing double-strand breaks at specific genetic locations. Through this action it participates in gene conversion processes allowing for the correction of genetic sequences. It does not operate as a part of a larger protein complex; rather its function centers on individual action and recognition of its target sites. Biological effectiveness makes it an attractive candidate for genomic studies and manipulations.

Pathways

I-SceI contributes significantly to DNA repair pathways particularly homologous recombination. This pathway is important for maintaining genomic stability. I-SceI cooperates with proteins such as RAD51 which facilitates strand exchange during the DNA repair process. In another pathway I-SceI-induced breaks can spur the activation of the single-strand annealing pathway when homologous recombination is impaired showcasing its versatile role in DNA repair mechanisms.

I-SceI's role in DNA repair connects it to cancer research. Impaired DNA repair mechanisms can lead to genomic instability a contributing factor to tumorigenesis. By enabling targeted gene corrections I-SceI may present therapeutic potential in correcting cancer-causing mutations. Additionally its interaction with the RAD51 protein implicates it in conditions where DNA repair is compromised such as certain genetic disorders with defective recombination.

Product protocols

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

Target data

Mitochondrial DNA endonuclease involved in intron homing. It introduces a specific double-strand break in the DNA of the 21S rRNA gene and thus mediates the insertion of an intron, containing its own coding sequence (group I intron), into an intronless gene. Specifically recognizes and cleaves the sequence 5'-TAGGGATAACAGGGTAAT-3'.
See full target information SCEI

Publications (3)

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

Nucleic acids research 48:10342-10352 PubMed32894284

2020

Hedgehog signaling enables repair of ribosomal DNA double-strand breaks.

Applications

WB

Species

Unspecified reactive species

Tshering D Lama-Sherpa,Victor T G Lin,Brandon J Metge,Shannon E Weeks,Dongquan Chen,Rajeev S Samant,Lalita A Shevde

The Journal of biological chemistry 293:12681-12689 PubMed29925587

2018

Mitochondrial accumulation of amyloid β (Aβ) peptides requires TOMM22 as a main Aβ receptor in yeast.

Applications

WB

Species

Unspecified reactive species

Wenxin Hu,Zhiming Wang,Hongjin Zheng

Nature communications 9:1016 PubMed29523790

2018

MRN complex-dependent recruitment of ubiquitylated BLM helicase to DSBs negatively regulates DNA repair pathways.

Applications

Unspecified application

Species

Unspecified reactive species

Vivek Tripathi,Himanshi Agarwal,Swati Priya,Harish Batra,Priyanka Modi,Monica Pandey,Dhurjhoti Saha,Sathees C Raghavan,Sagar Sengupta
View all publications

Product promise

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