LMNB1 Monoclonal Antibody

說明書

中文名稱：

LMNB1鼠單克隆抗體
貨號：

CSB-MA000191
規格：

￥1090
圖片：
1) Input: Mouse Brain Tissue Lysate 2) IP product: IP dilute 1:200

Western blot analysis of 1) HepG2, 2) 293T, 3) Mouse Brain Tissue, 4) Rat Brain Tissue, diluted at 1:5000.
其他：

產品詳情
產品評價
相關產品
靶點詳情

產品詳情

產品描述：

LMNB1單克隆抗體（CUSABIO貨號：CSB-MA000191）是針對核纖層蛋白B1（Lamin B1）研發的高特異性科研試劑，適用于人類、小鼠及大鼠樣本的檢測需求。LMNB1作為核纖層核心蛋白，在維持細胞核結構完整性、調控染色質空間排布及細胞周期進程中發揮關鍵作用，其表達異常與細胞衰老、基因組穩定性及多種退行性疾病密切相關。本產品基于雜交瘤技術制備，經嚴格驗證可應用于ELISA、Western Blot（WB）及免疫沉淀（IP）三大實驗平臺，能精準識別內源性LMNB1蛋白，為研究細胞核動態重塑、有絲分裂調控及衰老相關分子機制提供可靠工具。在神經退行性疾病模型、早衰癥研究及腫瘤細胞周期分析等科研場景中，該抗體可有效支持目標蛋白的定位、定量及相互作用研究，滿足分子生物學、細胞生物學領域的多層次實驗需求。通過優化抗體親和力與交叉反應控制，確保實驗結果的高重復性與跨平臺兼容性，是探索核纖層功能與疾病關聯的理想選擇。
Uniprot No.：

P20700
基因名：

LMNB1
別名：

ADLD antibody; lamin B1 antibody; Lamin-B1 antibody; LMN antibody; LMN2 antibody; LMNB antibody; Lmnb1 antibody; LMNB1_HUMAN antibody; MGC111419 antibody; OTTHUMP00000159218 antibody
宿主：

Mouse
反應種屬：

Human,Mouse,Rat
免疫原：

Recombinant Protein
免疫原種屬：

H, R, M
標記方式：

Non-conjugated
抗體亞型：

IgG
克隆號：

25D11
濃度：

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

PBS, 50% glycerol, 0.05% Proclin 300, 0.05%BSA
產品提供形式：

Liquid
應用范圍：

ELISA,WB,IP

推薦稀釋比：

Application	Recommended Dilution
WB	1:500-1:5000
IP	1:200-1:2000

Protocols：

ELISA Protocol
Western Blotting (WB) Protocol
Immunoprecipitation (IP) Protocol
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.

產品評價

靶點詳情

功能：

Lamins are components of the nuclear lamina, a fibrous layer on the nucleoplasmic side of the inner nuclear membrane, which is thought to provide a framework for the nuclear envelope and may also interact with chromatin.
基因功能參考文獻：
1. Results show that HECW2 interacts with lamin B1 mediating its ubiquitination and proteasomal degradation. PMID: 29753763
2. down-regulation of Lamin B1 and up-regulation of Nephroblastoma overexpressed (NOV) are at least partially responsible for the inhibitory effect of Huaier on the proliferative and invasive capacity of SKHEP-1 cells PMID: 27503760
3. The aim of the present study was to elucidate the influence of LMNB1 upregulation on colon cancer cell line after treatment with 5-FU. The results indicate, that overexpression of LMNB1 induced dose-dependent cell death mainly by mitotic catastrophe pathway. PMID: 29115590
4. We show that epithelial cells failing to undergo proliferation arrest during TGF-beta-induced EMT sustain mitotic abnormalities due to failed cytokinesis, resulting in aneuploidy. This genomic instability is associated with the suppression of multiple nuclear envelope proteins implicated in mitotic regulation and is phenocopied by modulating the expression of LaminB1. PMID: 27926867
5. An upstream mutation alters LMNB1 gene expression in autosomal dominant adult-onset demyelinating leukodystrophy. PMID: 25701871
6. Deregulation of LMNB1 expression induces modified splicing of several genes, likely driven by raver-2 overexpression, and suggest that an alteration of mRNA processing could be a pathogenic mechanism in adult-onset autosomal dominant leukodystrophy. PMID: 25637521
7. Lamin B1 levels are increased in oligodendrocytes, the cell type that produces myelin in the central nervous system. PMID: 26311780
8. Nuclear envelope remodelling during human spermiogenesis involves somatic B-type lamins and a spermatid-specific B3 lamin isoform. PMID: 25477337
9. LMNB1-related autosomal-dominant leukodystrophy is a slowly progressive neurological disease with survival lasting more than two decades after clinical onset. PMID: 26053668
10. Lamin B1 overexpression increases nuclear rigidity in autosomal dominant leukodystrophy fibroblasts. PMID: 24858279
11. Data indicate that lamin B1 promotes DNA double-strand breaks (DSBs) repair and cell survival. PMID: 25733566
12. maintenance of lamin B1 levels is required for DNA replication and repair through regulation of the expression of key factors involved in these essential nuclear functions PMID: 25535332
13. This led us to propose a model where the nucleolus has steady-state stiffness dependent on ribosome biogenesis activity and requires LaminB1 for its flexibility. PMID: 24297448
14. The regulation of lamin B1 is important for cellular physiology and disease.To how perturbations of lamin B1 affect cellular physiology and discuss the implications this has on senescence, HGPS and ADLD. PMID: 23873483
15. LMNB1 is required to maintain chromatin condensation in interphase nuclei. PMID: 24732130
16. Lamin B1 plays an important role in pancreatic cancer pathogenesis and is a novel therapeutic target of betulinic acid treatment. PMID: 23857605
17. we confirm the underlying role of lamin B1 duplication, regardless of the autonomic malfunction onset in Adult-onset autosomal dominant leukodystrophy PMID: 23681646
18. detailed molecular analysis of the largest collection of autosomal dominant leukodystrophy (ADLD) families studied, to date; identified the minimal duplicated region necessary for the disease, defined all the duplication junctions at the nucleotide level and identified the first inverted LMNB1 duplication PMID: 23649844
19. Rare variants of LMNB1 may contribute to susceptibility to neural tube defects. PMID: 23733478
20. lamin B1 down-regulation in senescence is a key trigger of global and local chromatin changes that impact gene expression, aging, and cancer PMID: 23934658
21. LMNB1 may contribute to senescence in at least two ways due to its uneven genome-wide redistribution: first, through the spatial reorganization of chromatin and, second, through gene repression. PMID: 23964094
22. Treating normal human fibroblasts with farnesyltransferase inhibitors causes the accumulation of unprocessed lamin B2 and lamin A and a decrease in mature lamin B1. PMID: 23475125
23. Results indicate that lamin B1 (LMNB1) accumulation in adult-onset autosomal dominant leukodystrophy (ADLD) is associated with Oct-1 recruitment. PMID: 23261988
24. LMNB1 protein levels decline in senescent human dermal fibroblasts and keratinocytes, mediated by reduced transcription and inhibition of LMNB1 messenger ribonucleic acid translation by miRNA-23a. PMID: 23439683
25. Lamin B1 is lost from primary human and murine cell strains when they are induced to senesce. PMID: 22496421
26. This study demonistrated that Adult-onset autosomal dominant leukodystrophy due to LMNB1 gene duplication. PMID: 21909802
27. The authors show that oxidative stress increases lamin B1 levels through p38 Mitogen Activated Protein kinase activation. PMID: 22246186
28. crystal structures of lamin B1 globular tail domain and coiled 2B domain, with similar folds to Ig-like domain and coiled-coil domain of lamin A. Found an extra intermolecular disulfide bond in lamin B1 coil 2B domain, which does not exist in lamin A/C. PMID: 22265972
29. LB1 expression in WI-38 cells decreases during cellular senescence PMID: 22155925
30. SNP array analysis revealed novel duplications spanning the entire LMNB1 gene in probands from each of four adult-onset autosomal dominant leukodystrophy families PMID: 21225301
31. Autosomal dominant leukodystrophy is the first disease that has ever been linked to lamin B1 mutations and it expands the pathological role of the nuclear lamia to include disorders of the brain. PMID: 20816241
32. results suggest that a LMNB1 regulatory sequence mutation underlies the variant adult-onset autosomal dominant leukodystrophy (ADLD) phenotype; adult forms of ADLD linked to 5q23 may be more heterogeneous clinically and genetically than previously thought PMID: 19961535
33. Proteomics identified lamin B1 as being significantly upregulated in HCC tumors and present in patients' plasma. PMID: 19522540
34. colocalizes with lamin B1 in the nucleoplasm and around the nuclear rim during S-phase of cells transfected with EBNA-1 in the absence of EBV plasmids. PMID: 12898336
35. organization of the nuclear envelope and lamina is dependent on a mechanism involving the methylation of lamin B1 PMID: 14504265
36. We now show that epitope masking in the nucleus is often responsible for failure to detect emerin and lamins in human, rat and pig tissues.These data suggest that different regions of the lamin B1 molecule are masked in different tissues. PMID: 16283426
37. Apoptotic neutrophils express lamin B1 on their surface; these cells may participate in the development of autoantibodies directed against cytoskeletal proteins, a condition frequently reported in several inflammatory diseases. PMID: 16365157
38. lamin B was essential for the formation of the mitotic matrix that tethers a number of spindle assembly factors; propose that lamin B is a structural component of the spindle matrix that promotes microtubule assembly and organization in mitosis PMID: 16543417
39. Results show that a lamin B1-containing nucleoskeleton is required to maintain RNA synthesis and that ongoing synthesis is a fundamental determinant of global nuclear architecture in mammalian cells. PMID: 18334554
40. Novel duplication on chromosomal band 5q23.2 in a French Canadian family with autosomal dominant leukodystrophy that supports the implication of duplicated LMNB1 as the disease-causing mutation. PMID: 19001169
41. duplication of the lamin B1 gene (LMNB1) has recently been described in a rare form of autosomal dominant adult-onset leukoencephalopathy. PMID: 19151023
42. Nudel regulates microtubule organization in part by facilitating assembly of the lamin B spindle matrix in a dynein-dependent manner. PMID: 19198602
43. Our work indicates that lamin B1 defects are probably not responsible for signs and symptoms resembling multiple sclerosis. PMID: 19348623
44. Lamin B1 maintains the functional plasticity of nucleoli. PMID: 19383719
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相關疾?。?/div>
Leukodystrophy, demyelinating, autosomal dominant, adult-onset (ADLD)
亞細胞定位：

Nucleus inner membrane; Lipid-anchor; Nucleoplasmic side.
蛋白家族：

Intermediate filament family
數據庫鏈接：

HGNC: 6637

OMIM: 150340

KEGG: hsa:4001

STRING: 9606.ENSP00000261366

UniGene: Hs.89497

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