| 產(chǎn)品編號 | bs-11001R |
| 英文名稱 | FAM61B Rabbit pAb |
| 中文名稱 | FAM61B蛋白抗體 |
| 別 名 | Protein FAM61B; Putative uncharacterized protein C20orf40; LSM14 homolog B(SCD6, S. cerevisiae); bA11M20.3; C20orf40; Chromosome 20 open reading frame 40; Family with sequence similarity 61 member B; LSM13; LSM14 homolog B; LSM14B SCD6 homolog B(S. cerevisiae); MGC61931; Protein LSM14 homolog B; RNA associated protein 55B; LS14B_HUMAN; LSM14B; bA11M20.3; C20orf40; FAM61B; FT005; LSM13; RAP55B. |
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Specific References (1) | bs-11001R has been referenced in 1 publications.
[IF=6.698] Tianqi Liu. et al. Genome-wide transcriptomics and copy number profiling identify patient-specific CNV-lncRNA-mRNA regulatory triplets in colorectal cancer. COMPUT BIOL MED. 2023 Feb;153:106545 WB ; Human.
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| 研究領(lǐng)域 | 細(xì)胞生物 免疫學(xué) 表觀遺傳學(xué) |
| 抗體來源 | Rabbit |
| 克隆類型 | Polyclonal |
| 克 隆 號 | |
| 交叉反應(yīng) | Rat (predicted: Human,Mouse,Cow,Dog) |
| 產(chǎn)品應(yīng)用 | Flow-Cyt=1μg/Test
not yet tested in other applications. optimal dilutions/concentrations should be determined by the end user. |
| 理論分子量 | 42 kDa |
| 檢測分子量 | |
| 性 狀 | Liquid |
| 濃 度 | 1mg/ml |
| 免 疫 原 | KLH conjugated synthetic peptide derived from human FAM61B: 251-350/385 |
| 亞 型 | IgG |
| 純化方法 | affinity purified by Protein A |
| 緩 沖 液 | 0.01M TBS (pH7.4) with 1% BSA, 0.02% Proclin300 and 50% Glycerol. |
| 保存條件 | Shipped at 4℃. Store at -20℃ for one year. Avoid repeated freeze/thaw cycles. |
| 注意事項 | This product as supplied is intended for research use only, not for use in human, therapeutic or diagnostic applications. |
| PubMed | PubMed |
| 產(chǎn)品介紹 |
Sm and Sm-like (LSm) proteins form donut-shaped, ubiquitously expressed heptameric complexes that are involved in various steps of RNA metabolism, including RNA-protein interactions and structural changes that are required during ribosomal subunit assembly. LSm14B, also known as C20orf40, FAM61B or LSM13, is a 385 amino acid protein that exists as multiple alternatively spliced isoforms and may play a role in RNA-related events. The gene encoding LSm14B maps to human chromosome 20. Comprising approximately 2% of the human genome, chromosome 20 contains nearly 63 million bases that encode over 600 genes, some of which are associated with Creutzfeldt-Jakob disease, amyotrophic lateral sclerosis, spinal muscular atrophy, ring chromosome 20 epilepsy syndrome and Alagille syndrome. Function: May play a role in control of mRNA translation (By similarity). Subunit: Component of a ribonucleoprotein (RNP) complex (By similarity). Similarity: Belongs to the LSM14 family. Contains 1 DFDF domain. SWISS: Q9BX40 Gene ID: 149986 Database links: Entrez Gene: 149986 Human Entrez Gene: 241846 Mouse SwissProt: Q9BX40 Human SwissProt: Q8CGC4 Mouse
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| 產(chǎn)品圖片 |
Blank control: RSC96(blue), the cells were fixed with 2% paraformaldehyde (10 min) and then permeabilized with ice-cold 90% methanol for 30 min on ice..
Isotype Control Antibody: Rabbit IgG(orange) ;
Secondary Antibody: Goat anti-rabbit IgG-FITC(white blue),
Dilution: 1:200 in 1 X PBS containing 0.5% BSA ;
Primary Antibody Dilution: 1μg in 100 μL1X PBS containing 0.5% BSA(green).
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