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AB5828

Anti-Y14抗体[4C4]

Anti-Y14 antibody [4C4]

5

(7 Reviews)

|

(9 Publications)

Mouse Monoclonal Y14 antibody. Suitable for IHC-P, ICC, Flow Cyt, WB and reacts with Human samples. Cited in 9 publications. Immunogen corresponding to Native Full Length Protein corresponding to Human RBM8A.

查看别名

RBM8, HSPC114, MDS014, RBM8A, RNA-binding protein 8A, Binder of OVCA1-1, RNA-binding motif protein 8A, RNA-binding protein Y14, Ribonucleoprotein RBM8A, BOV-1

4 Images
Western blot - Anti-Y14 antibody [4C4] (AB5828)
  • WB

Lab

Western blot - Anti-Y14 antibody [4C4] (AB5828)

All lanes:

Western blot - Anti-Y14 antibody [4C4] (ab5828) at 1 µg/mL

Lane 1:

HeLa (Human epithelial carcinoma cell line) Whole Cell Lysate at 10 µg

Lane 2:

Jurkat (Human T cell lymphoblast-like cell line) Whole Cell Lysate at 10 µg

Lane 3:

HepG2 (Human hepatocellular liver carcinoma cell line) Whole Cell Lysate at 10 µg

Lane 4:

HEK293 (Human embryonic kidney cell line) Whole Cell Lysate at 10 µg

Secondary

All lanes:

Western blot - Goat Anti-Mouse IgG H&L (HRP) preadsorbed (<a href='/products/secondary-antibodies/goat-mouse-igg-h-l-hrp-preadsorbed-ab97040'>ab97040</a>) at 1/5000 dilution

Predicted band size: 19 kDa

Observed band size: 21 kDa,53 kDa

true

Exposure time: 8min

Immunocytochemistry - Anti-Y14 antibody [4C4] (AB5828)
  • ICC

Lab

Immunocytochemistry - Anti-Y14 antibody [4C4] (AB5828)

ICC/IF image of ab5828 stained HeLa cells. The cells were 4% formaldehyde fixed (10 min) and then incubated in 1%BSA / 10% normal goat serum / 0.3M glycine in 0.1% PBS-Tween for 1h to permeabilise the cells and block non-specific protein-protein interactions. The cells were then incubated with the antibody (ab5828, 5µg/ml) overnight at +4°C. The secondary antibody (green) was Alexa Fluor® 488 goat anti-mouse IgG (H+L) used at a 1/1000 dilution for 1h. Alexa Fluor® 594 WGA was used to label plasma membranes (red) at a 1/200 dilution for 1h. DAPI was used to stain the cell nuclei (blue) at a concentration of 1.43µM.

Flow Cytometry - Anti-Y14 antibody [4C4] (AB5828)
  • Flow Cyt

Unknown

Flow Cytometry - Anti-Y14 antibody [4C4] (AB5828)

Overlay histogram showing HeLa cells stained with ab5828 (red line). The cells were fixed with 80% methanol (5 min) and then permeabilized with 0.1% PBS-Tween for 20 min. The cells were then incubated in 1x PBS / 10% normal goat serum / 0.3M glycine to block non-specific protein-protein interactions followed by the antibody (ab5828, 1μg/1x106 cells) for 30 min at 22°C. The secondary antibody used was DyLight® 488 goat anti-mouse IgG (H+L) (ab96879) at 1/500 dilution for 30 min at 22°C. Isotype control antibody (black line) was mouse IgG2b [PLPV219] (ab91366, 2μg/1x106 cells) used under the same conditions. Acquisition of >5,000 events was performed. This antibody gave a positive signal in HeLa cells fixed with 4% paraformaldehyde (10 min)/permeabilized with 0.1% PBS-Tween for 20 min used under the same conditions.

Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections) - Anti-Y14 antibody [4C4] (AB5828)
  • IHC-P

Unknown

Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections) - Anti-Y14 antibody [4C4] (AB5828)

IHC image of ab5828 staining in human kidney formalin fixed paraffin embedded tissue section, performed on a Leica BondTM system using the standard protocol F. The section was pre-treated using heat mediated antigen retrieval with sodium citrate buffer (pH6, epitope retrieval solution 1) for 20 mins. The section was then incubated with ab5828, 1µg/ml, for 15 mins at room temperature and detected using an HRP conjugated compact polymer system. DAB was used as the chromogen. The section was then counterstained with haematoxylin and mounted with DPX.

For other IHC staining systems (automated and non-automated) customers should optimize variable parameters such as antigen retrieval conditions, primary antibody concentration and antibody incubation times.

关键信息

宿主种属

Mouse

克隆

Monoclonal

克隆号

4C4

亚型

IgG2b

不含载体蛋白

No

反应种属

Human

应用

ICC, Flow Cyt, WB, IHC-P

applications

免疫原

Native Full Length Protein corresponding to Human RBM8A.

Q9Y5S9

反应性数据

{ "title": "Reactivity Data", "filters": { "stats": ["", "Species", "Dilution Info", "Notes"], "tabs": { "all-applications": {"fullname" : "All Applications", "shortname": "All Applications"}, "IHCP" : {"fullname" : "Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections)", "shortname":"IHC-P"}, "ICC" : {"fullname" : "Immunocytochemistry", "shortname":"ICC"}, "FlowCyt" : {"fullname" : "Flow Cytometry", "shortname":"Flow Cyt"}, "WB" : {"fullname" : "Western blot", "shortname":"WB"} }, "product-promise": { "all": "all", "testedAndGuaranteed": "tested", "guaranteed": "expected", "predicted": "predicted", "notRecommended": "not-recommended" } }, "values": { "Human": { "IHCP-species-checked": "testedAndGuaranteed", "IHCP-species-dilution-info": "1 µg/mL", "IHCP-species-notes": "<p></p> Perform heat-mediated antigen retrieval with citrate buffer pH 6 before commencing with IHC staining protocol.", "ICC-species-checked": "testedAndGuaranteed", "ICC-species-dilution-info": "", "ICC-species-notes": "<p></p>", "FlowCyt-species-checked": "testedAndGuaranteed", "FlowCyt-species-dilution-info": "1-2 µg for 10^6 Cells", "FlowCyt-species-notes": "<p><a href='/products/primary-antibodies/mouse-igg2b-kappa-monoclonal-7e10g10-isotype-control-ab170192'>ab170192</a> - Mouse monoclonal IgG2b, is suitable for use as an isotype control with this antibody.</p>", "WB-species-checked": "testedAndGuaranteed", "WB-species-dilution-info": "", "WB-species-notes": "<p></p>" } } }

性能和储存信息

形式
Liquid
纯化工艺
Affinity purification Protein A
纯化说明
Purified from tissue culture supernatant.
存储溶液
Preservative: 0.1% Sodium azide Constituents: PBS
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
-20°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.

Y14 also known as RBM8A is a protein integral to the exon junction complex (EJC) with an approximate mass of 18 kDa. It localizes mainly in the nucleus of cells. Y14 works with other proteins such as MAGOH serving a role in post-splicing mRNA regulation. Across various tissues Y14 shows expression but is particularly notable in tissues with high levels of mRNA processing like the brain and testis.
Biological function summary

Y14 functions in mRNA surveillance and quality control mechanisms. It forms part of the exon junction complex a multi-protein structure deposited on mRNA after splicing occurs. The component acts importantly in nonsense-mediated mRNA decay (NMD) a process that ensures defective mRNAs do not translate into dysfunctional proteins. Y14 contributes significantly to mRNA export from the nucleus binding to spliced mRNA and guiding them towards translation sites in the cytoplasm.

Pathways

Y14 plays a significant role in the nonsense-mediated mRNA decay pathway working in tandem with proteins such as UPF1 and UPF3. This pathway helps identify and degrade mRNA transcripts with premature stop codons therefore protecting cells from expressing truncated proteins that may disrupt normal cellular functions. Moreover Y14 is linked to the mRNA export pathway ensuring that only properly spliced messages reach the ribosome for translation.

Y14 relevance appears in relation to neurodevelopmental disorders and certain cancers. Mutations or dysregulation of Y14 might contribute to conditions such as intellectual disability due to its involvement in mRNA surveillance that affects neuronal development. Additionally aberrant expression of Y14 has connections to breast cancer where it interacts with proteins involved in altered signaling pathways impacting cancer progression and metastasis.

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

Required for pre-mRNA splicing as component of the spliceosome (PubMed : 28502770, PubMed : 29301961). Core component of the splicing-dependent multiprotein exon junction complex (EJC) deposited at splice junctions on mRNAs. The EJC is a dynamic structure consisting of core proteins and several peripheral nuclear and cytoplasmic associated factors that join the complex only transiently either during EJC assembly or during subsequent mRNA metabolism. The EJC marks the position of the exon-exon junction in the mature mRNA for the gene expression machinery and the core components remain bound to spliced mRNAs throughout all stages of mRNA metabolism thereby influencing downstream processes including nuclear mRNA export, subcellular mRNA localization, translation efficiency and nonsense-mediated mRNA decay (NMD). The MAGOH-RBM8A heterodimer inhibits the ATPase activity of EIF4A3, thereby trapping the ATP-bound EJC core onto spliced mRNA in a stable conformation. The MAGOH-RBM8A heterodimer interacts with the EJC key regulator PYM1 leading to EJC disassembly in the cytoplasm and translation enhancement of EJC-bearing spliced mRNAs by recruiting them to the ribosomal 48S preinitiation complex. Its removal from cytoplasmic mRNAs requires translation initiation from EJC-bearing spliced mRNAs. Associates preferentially with mRNAs produced by splicing. Does not interact with pre-mRNAs, introns, or mRNAs produced from intronless cDNAs. Associates with both nuclear mRNAs and newly exported cytoplasmic mRNAs. The MAGOH-RBM8A heterodimer is a component of the nonsense mediated decay (NMD) pathway. Involved in the splicing modulation of BCL2L1/Bcl-X (and probably other apoptotic genes); specifically inhibits formation of proapoptotic isoforms such as Bcl-X(S); the function is different from the established EJC assembly.
See full target information RBM8A

文献 (9)

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

Nature communications 13:7904 PubMed36550132

2022

Exon junction complex shapes the mA epitranscriptome.

Applications

Unspecified application

Species

Unspecified reactive species

Xin Yang,Robinson Triboulet,Qi Liu,Erdem Sendinc,Richard I Gregory

iScience 25:105270 PubMed36304109

2022

A seven-transmembrane protein-TM7SF3, resides in nuclear speckles and regulates alternative splicing.

Applications

Unspecified application

Species

Unspecified reactive species

Roi Isaac,Yaron Vinik,Martin Mikl,Shani Nadav-Eliyahu,Hadas Shatz-Azoulay,Adi Yaakobi,Natalie DeForest,Amit R Majithia,Nicholas J G Webster,Yaron Shav-Tal,Eytan Elhanany,Yehiel Zick

iScience 24:103368 PubMed34816104

2021

The Y14-p53 regulatory circuit in megakaryocyte differentiation and thrombocytopenia.

Applications

Unspecified application

Species

Unspecified reactive species

Chun-Hao Su,Wei-Ju Liao,Wei-Chi Ke,Ruey-Bing Yang,Woan-Yuh Tarn

Cells 9: PubMed32854341

2020

The Sub-Nuclear Localization of RNA-Binding Proteins in KSHV-Infected Cells.

Applications

Unspecified application

Species

Unspecified reactive species

Ella Alkalay,Chen Gam Ze Letova Refael,Irit Shoval,Noa Kinor,Ronit Sarid,Yaron Shav-Tal

Scientific reports 8:9646 PubMed29941967

2018

Accumulation of poly(A) RNA in nuclear granules enriched in Sam68 in motor neurons from the SMNΔ7 mouse model of SMA.

Applications

Unspecified application

Species

Unspecified reactive species

J Oriol Narcís,Olga Tapia,Olga Tarabal,Lídia Piedrafita,Jordi Calderó,Maria T Berciano,Miguel Lafarga

Neurobiology of disease 108:83-99 PubMed28823932

2017

Cellular bases of the RNA metabolism dysfunction in motor neurons of a murine model of spinal muscular atrophy: Role of Cajal bodies and the nucleolus.

Applications

Unspecified application

Species

Unspecified reactive species

Olga Tapia,Josep Oriol Narcís,Javier Riancho,Olga Tarabal,Lídia Piedrafita,Jordi Calderó,Maria T Berciano,Miguel Lafarga

The Journal of biological chemistry 282:15645-51 PubMed17363367

2007

The interaction between cap-binding complex and RNA export factor is required for intronless mRNA export.

Applications

Unspecified application

Species

Unspecified reactive species

Takayuki Nojima,Tetsuro Hirose,Hiroshi Kimura,Masatoshi Hagiwara

Chromosoma 116:53-64 PubMed17103222

2006

FRG1P-mediated aggregation of proteins involved in pre-mRNA processing.

Applications

Unspecified application

Species

Unspecified reactive species

Silvana van Koningsbruggen,Kirsten R Straasheijm,Ellen Sterrenburg,Natascha de Graaf,Hans G Dauwerse,Rune R Frants,Silvère M van der Maarel

The Journal of cell biology 172:373-81 PubMed16431928

2006

In vivo BiFC analysis of Y14 and NXF1 mRNA export complexes: preferential localization within and around SC35 domains.

Applications

WB

Species

Human

Ute Schmidt,Karsten Richter,Axel Bernhard Berger,Peter Lichter
View all publications

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