癌症的基本特征包括细胞增殖、血管生成、迁移、凋亡逃避机制和细胞永生等。找到癌症发生过程中这些通路的关键标记物和对应的抗体用于检测至关重要。
为您推荐一个泛素化位点预测神器——泛素化分析工具，可以为您的蛋白的泛素化位点作出预测和评分。
细胞自噬受体图形绘图工具为你的蛋白的细胞受体结合位点作出预测和评分，识别结合到自噬通路中的蛋白是非常重要的，便于让我们理解自噬在正常生理、病理过程中的作用，如发育、细胞分化、神经退化性疾病、压力条件下、感染和癌症。
NOL4 Rabbit pAb
NOL4 Rabbit pAb
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- 实验流程
- 背景知识
Application 
| IHC-P, IHC-F, IF |
|---|---|
| Primary Accession | O94818 |
| Reactivity | Mouse |
| Predicted | Human, Rat, Dog, Rabbit, Sheep |
| Host | Rabbit |
| Clonality | Polyclonal |
| Calculated MW | 71357 Da |
| Physical State | Liquid |
| Immunogen | KLH conjugated synthetic peptide derived from human NOL4 |
| Epitope Specificity | 1-100/638 |
| Isotype | IgG |
| Purity | affinity purified by Protein A |
| Buffer | 0.01M TBS (pH7.4) with 1% BSA, 0.02% Proclin300 and 50% Glycerol. |
| SUBCELLULAR LOCATION | Nucleus > nucleolus. |
| Important Note | This product as supplied is intended for research use only, not for use in human, therapeutic or diagnostic applications. |
| Background Descriptions | NOL4 is a 524 amino acid protein that is predominantly expressed in testis and brain. NOL4 contains at least two domains that direct it to subnuclear locations. The gene encoding NOL4 is located on human chromosome 18, which houses over 300 protein-coding genes and contains nearly 76 million bases. There are a variety of diseases associated with defects in chromosome 18-localized genes, some of which include Trisomy 18 (also known as Edwards syndrome), Niemann-Pick disease, hereditary hemorrhagic telangiectasia, erythropoietic protoporphyria and follicular lymphomas. There are two isoforms of NOL4 that are produced as a result of alternative splicing events. |
| Gene ID | 8715 |
|---|---|
| Other Names | Nucleolar protein 4, Nucleolar-localized protein, NOL4, NOLP |
| Target/Specificity | Expressed predominantly in fetal brain, adult brain and testis. |
| Dilution | IHC-P=1:100-500,IHC-F=1:100-500,IF=1:100-500 |
| Storage | Store at -20 °C for one year. Avoid repeated freeze/thaw cycles. When reconstituted in sterile pH 7.4 0.01M PBS or diluent of antibody the antibody is stable for at least two weeks at 2-4 °C. |
| Name | NOL4 |
|---|---|
| Synonyms | NOLP |
| Cellular Location | Nucleus, nucleolus |
| Tissue Location | Expressed predominantly in fetal brain, adult brain and testis. |
For Research Use Only. Not For Use In Diagnostic Procedures.
Provided below are standard protocols that you may find useful for product applications.
BACKGROUND
NOL4 is a 524 amino acid protein that is predominantly expressed in testis and brain. NOL4 contains at least two domains that direct it to subnuclear locations. The gene encoding NOL4 is located on human chromosome 18, which houses over 300 protein-coding genes and contains nearly 76 million bases. There are a variety of diseases associated with defects in chromosome 18-localized genes, some of which include Trisomy 18 (also known as Edwards syndrome), Niemann-Pick disease, hereditary hemorrhagic telangiectasia, erythropoietic protoporphyria and follicular lymphomas. There are two isoforms of NOL4 that are produced as a result of alternative splicing events.
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