RBM10 Antibody, FITC conjugated

說明書

中文名稱：

RBM10兔多克隆抗體, FITC偶聯(lián)
貨號：

CSB-PA019400LC01HU
規(guī)格：

￥880
其他：

產(chǎn)品詳情
產(chǎn)品評價
相關(guān)產(chǎn)品
靶點詳情

產(chǎn)品詳情

產(chǎn)品名稱：

Rabbit anti-Homo sapiens (Human) RBM10 Polyclonal antibody
Uniprot No.：

P98175
基因名：

RBM10
別名：

DXS8237E antibody; G patch domain containing protein 9 antibody; G patch domain-containing protein 9 antibody; GPATC9 antibody; GPATCH9 antibody; HGNC9896 antibody; KIAA0122 antibody; MGC1132 antibody; MGC997 antibody; Rbm10 antibody; RBM10_HUMAN antibody; RNA binding motif protein 10 antibody; RNA binding protein 10 antibody; RNA binding protein S1-1 antibody; RNA-binding motif protein 10 antibody; RNA-binding protein 10 antibody; RNA-binding protein S1-1 antibody; S1-1 antibody; TARPS antibody; ZRANB5 antibody
宿主：

Rabbit
反應(yīng)種屬：

Human
免疫原：

Recombinant Human RNA-binding protein 10 protein (501-700AA)
免疫原種屬：

Homo sapiens (Human)
標(biāo)記方式：

FITC
克隆類型：

Polyclonal
抗體亞型：

IgG
純化方式：

>95%, Protein G purified
濃度：

It differs from different batches. Please contact us to confirm it.
保存緩沖液：

Preservative: 0.03% Proclin 300
Constituents: 50% Glycerol, 0.01M PBS, PH 7.4
產(chǎn)品提供形式：

Liquid
儲存條件：

Upon receipt, store at -20°C or -80°C. Avoid repeated freeze.
貨期：

Basically, we can dispatch the products out in 1-3 working days after receiving your orders. Delivery time maybe differs from different purchasing way or location, please kindly consult your local distributors for specific delivery time.
用途：

For Research Use Only. Not for use in diagnostic or therapeutic procedures.

產(chǎn)品評價

靶點詳情

功能：

May be involved in post-transcriptional processing, most probably in mRNA splicing. Binds to RNA homopolymers, with a preference for poly(G) and poly(U) and little for poly(A). May bind to specific miRNA hairpins.
基因功能參考文獻：
1. RBM10: Harmful or helpful-many factors to consider. PMID: 29274279
2. RBM10 mutations contribute to lung adenocarcinoma pathogenesis. PMID: 28091594
3. The high rate of TERT promoter mutations, MED12 mutations, RBM10 mutations, and chromosome 1q gain highlight their likely association with tumor virulence PMID: 28634282
4. The well-known high-fidelity RNA splice site recognition by RBM10, and probably by RBM5 and RBM6, can thus be largely rationalized by a cooperative binding action of RRM and ZnF domains PMID: 29450990
5. Our work has not only expanded the number of pre-mRNA targets for RBM10, but identified RBM10 as a novel regulator of SMN2 alternative inclusion. PMID: 28728573
6. RBM10 functions as a splicing regulator using two RNA-binding units with different specificities to promote exon skipping. PMID: 28379442
7. RNA binding motif protein 10 (RBM10) negatively regulates its own mRNA and protein expression and that of RNA binding motif protein 5 (RBM5) by promoting alternative splicing-coupled nonsense-mediated mRNA decay (AS-NMD). PMID: 28586478
8. results provide evidence that RBM10 expression, in RBM5-null tumors, may contribute to tumor growth and metastasis. Measurement of both RBM10 and RBM5 expression in clinical samples may therefore hold prognostic and/or potentially predictive value PMID: 28662214
9. RBM10-TFE3 is a recurrent gene fusion in Xp11 translocation renal cell carcinoma. PMID: 28296677
10. Xp11 translocation renal cell carcinomas with RBM10-TFE3 gene fusion demonstrating melanotic features and overlapping morphology with t(6;11) RCC. PMID: 28288037
11. RNA-binding motif 10 messenger RNA and protein were reduced in lung adenocarcinoma tissues, and RNA-binding motif 10 overexpression inhibited lung adenocarcinoma cancer cell malignant behavior in vitro. Molecularly, RNA-binding motif 10 regulates many gene pathways involving in the tumor development or progression. PMID: 28347232
12. RBM10-TFE3 fusion variant (from chromosome X paracentric inversion), therefore, appears to be a recurrent molecular event in Xp11.2 RCCs. RBM10-TFE3 fusion should be added in the list of screened fusion transcripts in targeted molecular diagnostic multiplex RT-PCR PMID: 26998913
13. RBM10 is a tumor suppressor that represses Notch signaling and cell proliferation through the regulation of NUMB alternative splicing PMID: 26853560
14. Src family tyrosine kinase signaling may regulate FilGAP through association with RBM10 PMID: 26751795
15. The ability of RBM10v1 to regulate alternative splicing depends, at least in part, on a structural alteration within the second RNA recognition motif domain, and correlates with preferential expression of the NUMB exon 11 inclusion variant. PMID: 25889998
16. RBM10 regulates alternative splicing of Fas and Bcl-x genes. PMID: 24530524
17. Antagonizes the effects of RBM5, RBM6, and RBM10 in cell colony formation. PMID: 24332178
18. This study established RBM10 as an important regulator of alternative splicing, presented a mechanistic model for RBM10-mediated splicing regulation and provided a molecular link to understanding a human congenital disorder. PMID: 24000153
19. S1-1 contains multiple nuclear localisation sequence that act cooperatively. PMID: 23294349
20. Massively parallel sequencing of exons on the X chromosome identifies RBM10 as the gene that causes a syndromic form of cleft palate. PMID: 20451169
21. From these results, it seems that the X-chromosome, through its RBM genes, plays a formerly unknown role in the regulation of programmed cell death (apoptosis) in breast cancer. PMID: 16552754
22. S1-1 constitutes hundreds of nuclear domains, which dynamically change their structures in a reversible manner; upon globally reducing RNA polymerase II transcription, S1-1 nuclear bodies enlarge and decrease in number. PMID: 18315527
23. results indicate that very few genes are involved in the last steps of the apoptotic cascade in breast cancer, among them one of the X-chromosome RBM family PMID: 18820371
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相關(guān)疾病：

TARP syndrome (TARPS)
亞細胞定位：

Nucleus. Note=In the extranucleolar nucleoplasm constitutes hundreds of nuclear domains, which dynamically change their structures in a reversible manner. Upon globally reducing RNA polymerase II transcription, the nuclear bodies enlarge and decrease in number. They occur closely adjacent to nuclear speckles or IGCs (interchromatin granule clusters) but coincide with TIDRs (transcription-inactivation-dependent RNA domains).
數(shù)據(jù)庫鏈接：

HGNC: 9896

OMIM: 300080

KEGG: hsa:8241

STRING: 9606.ENSP00000366829

UniGene: Hs.401509

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