| 產(chǎn)品編號 | bs-15551R |
| 英文名稱(chēng) | Rabbit Anti-IFI44L antibody |
| 中文名稱(chēng) | 干擾素誘導蛋白44樣蛋白抗體 |
| 別 名 | C1orf29; GS3686; IF44L_HUMAN; IFI44L; Interferon-induced protein 44-like. |
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Specific References (1) | bs-15551R has been referenced in 1 publications.
[IF=5.923] Cheng Chen. et al. Identified Three Interferon Induced Proteins as Novel Biomarkers of Human Ischemic Cardiomyopathy. Int J Mol Sci. 2021 Jan;22(23):13116 ELISA,IHC ; Rat.
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| 研究領(lǐng)域 | 細胞生物 微生物學(xué) 細胞因子 |
| 抗體來(lái)源 | Rabbit |
| 克隆類(lèi)型 | Polyclonal |
| 交叉反應 | Human |
| 產(chǎn)品應用 | WB=1:500-2000
not yet tested in other applications. optimal dilutions/concentrations should be determined by the end user. |
| 理論分子量 | 51kDa |
| 細胞定位 | 細胞漿 |
| 性 狀 | Liquid |
| 濃 度 | 1mg/ml |
| 免 疫 原 | KLH conjugated synthetic peptide derived from human IFI44L: 101-200/452 |
| 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 |
IFI-44L is a 452 amino acid cytoplasmic protein that shares some sequence similarities with IFI-44. IFI-44 is a cytoplasmic protein that aggregates to form microtubule structures. The genes that encode IFI-44L and IFI-44 are located on chromosome 1, which is the largest human chromosome spanning about 260 million base pairs and making up 8% of the human genome. There are about 3,000 genes on chromosome 1, and considering the great number of genes there are also a large number of diseases associated with chromosome 1. Notably, the rare aging disease Hutchinson-Gilford progeria is associated with the LMNA gene which encodes lamin A. When defective, the LMNA gene product can build up in the nucleus and cause characteristic nuclear blebs. The mechanism of rapidly enhanced aging is unclear and is a topic of continuing exploration. Stickler syndrome, Parkinsons, Gaucher disease and Usher syndrome are also associated with chromosome 1. Aberrations in chromosome 1 are found in a variety of cancers including head and neck cancer, malignant melanoma and multiple myeloma. Function: Exhibits a low antiviral activity against hepatitis C virus. Subcellular Location: Cytoplasm (Potential). Similarity: Belongs to the IFI44 family. SWISS: Q53G44 Gene ID: 10964 Database links: Entrez Gene: 10964 Human Omim: 613975 Human SwissProt: Q53G44 Human Unigene: 731680 Human |
| 產(chǎn)品圖片 |
Sample: Du145 Cell (Human) Lysate at 30 ug
Primary: Anti-IFI44L (bs-15551R) at 1/300 dilution
Secondary: IRDye800CW Goat Anti-Rabbit IgG at 1/20000 dilution
Predicted band size: 51kD
Observed band size: 51kD
Sample:MCF-7 Cell (Human) Lysate at 30 ug
Primary: Anti-IFI44L (bs-15551R) at 1/300 dilution
Secondary: IRDye800CW Goat Anti-Rabbit IgG at 1/20000 dilution
Predicted band size: 51kD
Observed band size: 51kD
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