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AB241589

Anti-SNRNP200抗体

Anti-SNRNP200 antibody

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(6 Publications)

Rabbit Polyclonal SNRNP200 antibody. Suitable for IP, WB, IHC-P and reacts with Human, Mouse samples. Cited in 6 publications. Immunogen corresponding to Synthetic Peptide within Human SNRNP200 aa 1-50.

查看别名

ASCC3L1, BRR2, HELIC2, KIAA0788, SNRNP200, U5 small nuclear ribonucleoprotein 200 kDa helicase, Activating signal cointegrator 1 complex subunit 3-like 1, BRR2 homolog, U5 snRNP-specific 200 kDa protein, U5-200KD

3 Images
Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections) - Anti-SNRNP200 antibody (AB241589)
  • IHC-P

Supplier Data

Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections) - Anti-SNRNP200 antibody (AB241589)

Formalin-fixed, paraffin-embedded human colon carcinoma tissue stained for SNRNP200 using ab241589 at 1/200 dilution in immunohistochemical analysis. DAB staining. Counterstained with Hematoxylin.

Immunoprecipitation - Anti-SNRNP200 antibody (AB241589)
  • IP

Supplier Data

Immunoprecipitation - Anti-SNRNP200 antibody (AB241589)

SNRNP200 was immunoprecipitated from HeLa (human epithelial cell line from cervix adenocarcinoma) whole cell lyste (1 mg for IP, 20% of IP loaded) using ab241589 at 6 μg/mg lysate. Western blot was performed on the immunoprecipitate using ab241589 at 0.4 μg/mL.

Lane 1 : ab241589 IP in HeLa whole cell lysate.
Lane 2 : Control IgG in HeLa whole cell lysate.

Detection : Chemiluminescence with an exposure time of 3 seconds.

All lanes:

Immunoprecipitation - Anti-SNRNP200 antibody (ab241589)

Predicted band size: 245 kDa

false

Western blot - Anti-SNRNP200 antibody (AB241589)
  • WB

Supplier Data

Western blot - Anti-SNRNP200 antibody (AB241589)

All lanes:

Western blot - Anti-SNRNP200 antibody (ab241589) at 0.04 µg/mL

Lane 1:

HeLa (human epithelial cell line from cervix adenocarcinoma) whole cell lysate at 50 µg

Lane 2:

HeLa whole cell lysate at 15 µg

Lane 3:

HEK-293T (human epithelial cell line from embryonic kidney transformed with large T antigen) whole cell lysate at 50 µg

Lane 4:

Jurkat (human T cell leukemia cell line from peripheral blood) whole cell lysate at 50 µg

Lane 5:

NIH/3T3 (mouse embryo fibroblast cell line) whole cell lysate at 50 µg

Predicted band size: 245 kDa

true

Exposure time: 10s

关键信息

宿主种属

Rabbit

克隆

Polyclonal

亚型

IgG

不含载体蛋白

No

反应种属

Mouse, Human

应用

IP, IHC-P, WB

applications

免疫原

Synthetic Peptide within Human SNRNP200 aa 1-50. The exact immunogen used to generate this antibody is proprietary information.

O75643

反应性数据

{ "title": "Reactivity Data", "filters": { "stats": ["", "Species", "Dilution Info", "Notes"], "tabs": { "all-applications": {"fullname" : "All Applications", "shortname": "All Applications"}, "IP" : {"fullname" : "Immunoprecipitation", "shortname":"IP"}, "WB" : {"fullname" : "Western blot", "shortname":"WB"}, "IHCP" : {"fullname" : "Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections)", "shortname":"IHC-P"} }, "product-promise": { "all": "all", "testedAndGuaranteed": "tested", "guaranteed": "expected", "predicted": "predicted", "notRecommended": "not-recommended" } }, "values": { "Human": { "IP-species-checked": "testedAndGuaranteed", "IP-species-dilution-info": "2-10 µg/mg of lysate", "IP-species-notes": "<p></p>", "WB-species-checked": "testedAndGuaranteed", "WB-species-dilution-info": "1/2000 - 1/10000", "WB-species-notes": "<p></p>", "IHCP-species-checked": "testedAndGuaranteed", "IHCP-species-dilution-info": "1/100 - 1/500", "IHCP-species-notes": "<p>Epitope retrieval with citrate buffer pH 6.0 is recommended for FFPE tissue sections.</p>" }, "Mouse": { "IP-species-checked": "guaranteed", "IP-species-dilution-info": "", "IP-species-notes": "", "WB-species-checked": "testedAndGuaranteed", "WB-species-dilution-info": "1/2000 - 1/10000", "WB-species-notes": "<p></p>", "IHCP-species-checked": "guaranteed", "IHCP-species-dilution-info": "", "IHCP-species-notes": "" }, "Rat": { "IP-species-checked": "predicted", "IP-species-dilution-info": "", "IP-species-notes": "", "WB-species-checked": "predicted", "WB-species-dilution-info": "", "WB-species-notes": "", "IHCP-species-checked": "predicted", "IHCP-species-dilution-info": "", "IHCP-species-notes": "" } } }

性能和储存信息

形式
Liquid
纯化工艺
Affinity purification Immunogen
纯化说明
Antibody was affinity purified using an epitope specific to SNRNP200 immobilized on solid support.
存储溶液
pH: 6.8 - 7.4 Preservative: 0.09% Sodium azide Constituents: Tris buffered saline, 0.1% BSA
运输条件
Blue Ice
推荐的短期储存时间
1-2 weeks
推荐的短期储存条件
+4°C
推荐的长期储存条件
+4°C
分装信息
Upon delivery aliquot
储存信息
Avoid freeze / thaw cycle

补充信息

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

SNRNP200 also known as BRR2 or hBrr2 is an essential part of the spliceosome machinery. It is a large protein with a mass of approximately 250 kDa. The protein is widely expressed in various tissues with high levels in cells that have robust splicing activity. SNRNP200 is an ATPase and helicase and its mechanical role involves unwinding RNA duplexes during pre-mRNA splicing. Its activity is necessary for the rearrangements within the spliceosome facilitating the transition between different stages of the splicing cycle.
Biological function summary

SNRNP200 facilitates pre-mRNA splicing by being part of the U5 small nuclear ribonucleoprotein (snRNP) complex. The protein helps in the unwinding of RNA helices allowing snRNPs to correctly assemble and disassemble on pre-mRNA substrates. Efficient pre-mRNA splicing by SNRNP200 ensures accurate removal of introns and joining of exons leading to mature mRNA production. SNRNP200 collaborates with other spliceosomal components to maintain fidelity in the splicing process which is important for gene expression regulation.

Pathways

SNRNP200 plays integral roles in the splicing pathway and RNA processing pathway. Within the splicing pathway it interacts closely with several other spliceosomal proteins including PRPF8 and EFTUD2 to modulate spliceosome dynamics. These interactions facilitate the precise and timely execution of splicing events. The RNA processing pathway involves intricate networks of proteins where SNRNP200's helicase activity is critical for processing precursor mRNAs into mature forms for translation.

Abnormalities associated with SNRNP200 have been linked to retinitis pigmentosa and certain forms of glaucoma. Mutations in the gene encoding SNRNP200 can lead to defects in RNA splicing which in turn disrupts the expression of proteins necessary for retinal health and function. This protein also interacts with other proteins like PRPF31 and PRPF8 which are associated with similar retinal degenerative disorders. Understanding SNRNP200's role in these diseases provides insight into the molecular mechanisms underlying specific vision-related pathologies.

产品实验方案

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

靶点信息

Catalyzes the ATP-dependent unwinding of U4/U6 RNA duplices, an essential step in the assembly of a catalytically active spliceosome (PubMed : 35241646). Plays a role in pre-mRNA splicing as a core component of precatalytic, catalytic and postcatalytic spliceosomal complexes (PubMed : 28502770, PubMed : 28781166, PubMed : 29301961, PubMed : 29360106, PubMed : 29361316, PubMed : 30315277, PubMed : 30705154, PubMed : 30728453). As a component of the minor spliceosome, involved in the splicing of U12-type introns in pre-mRNAs (Probable). Involved in spliceosome assembly, activation and disassembly. Mediates changes in the dynamic network of RNA-RNA interactions in the spliceosome.
See full target information SNRNP200

文献 (6)

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

Cell discovery 10:96 PubMed39285160

2024

Targeting SNRNP200-induced splicing dysregulation offers an immunotherapy opportunity for glycolytic triple-negative breast cancer.

Applications

Unspecified application

Species

Unspecified reactive species

Wenxiao Yang,Luo Hong,Linwei Guo,Yunjin Wang,Xiangchen Han,Boyue Han,Zheng Xing,Guoliang Zhang,Hongxia Zhou,Chao Chen,Hong Ling,Zhimin Shao,Xin Hu

Cell cycle (Georgetown, Tex.) 22:986-1004 PubMed36762777

2023

Metformin attenuates multiple myeloma cell proliferation and encourages apoptosis by suppressing METTL3-mediated m6A methylation of THRAP3, RBM25, and USP4.

Applications

Unspecified application

Species

Unspecified reactive species

Cong-Jie Chen,Jie-Yun Huang,Jian-Qing Huang,Jia-Yi Deng,Xiao-Hui Shangguan,Ai-Zhen Chen,Long-Tian Chen,Wei-Hao Wu

Nucleic acids research 50:5263-5281 PubMed35489070

2022

Reovirus μ2 protein modulates host cell alternative splicing by reducing protein levels of U5 snRNP core components.

Applications

Unspecified application

Species

Unspecified reactive species

Simon Boudreault,Mathieu Durand,Carole-Anne Martineau,Jean-Pierre Perreault,Guy Lemay,Martin Bisaillon

Frontiers in cell and developmental biology 9:759192 PubMed34790668

2021

miR-6807-5p Inhibited the Odontogenic Differentiation of Human Dental Pulp Stem Cells Through Directly Targeting METTL7A.

Applications

Unspecified application

Species

Unspecified reactive species

Ning Wang,Xiao Han,Haoqing Yang,Dengsheng Xia,Zhipeng Fan

Journal of translational medicine 18:209 PubMed32448371

2020

microRNA-1271 impedes the development of prostate cancer by downregulating PES1 and upregulating ERβ.

Applications

Unspecified application

Species

Unspecified reactive species

Zhenming Jiang,Yuxi Zhang,Xi Chen,Yan Wang,Pingeng Wu,Chengzhang Wu,Dong Chen

EBioMedicine 51:102547 PubMed31902674

2020

Dysregulation of the splicing machinery is directly associated to aggressiveness of prostate cancer.

Applications

Unspecified application

Species

Unspecified reactive species

Juan M Jiménez-Vacas,Vicente Herrero-Aguayo,Antonio J Montero-Hidalgo,Enrique Gómez-Gómez,Antonio C Fuentes-Fayos,Antonio J León-González,Prudencio Sáez-Martínez,Emilia Alors-Pérez,Sergio Pedraza-Arévalo,Teresa González-Serrano,Oscar Reyes,Ana Martínez-López,Rafael Sánchez-Sánchez,Sebastián Ventura,Elena M Yubero-Serrano,María J Requena-Tapia,Justo P Castaño,Manuel D Gahete,Raúl M Luque
View all publications

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