p53/CEN17q FISH Probe
产品名称: p53/CEN17q FISH Probe
英文名称: p53/CEN17q FISH Probe
产品编号: FG0011
产品价格: 0
产品产地: 台湾
品牌商标: Abnova
更新时间: null
使用范围: null
亚诺法生技股份有限公司(Abnova)
- 联系人 :
- 地址 : 台湾台北市内湖区洲子街 108 号 9 楼
- 邮编 : 11493
- 所在区域 : 台湾
- 电话 : +886-920**1152 点击查看
- 传真 : 点击查看
- 邮箱 : sales@abnova.com.tw
- Specification
- Product Description:
- Labeled FISH probes for identification of gene amplification using Fluoresecent In Situ Hybridization Technique. (Technology)
- Storage Instruction:
- Store at 4°C in the dark.
- Quality Control Testing:
- Representative images of normal human cell (lymphocyte) stain with the dual color FISH probe. The left image is chromosomes at metaphase, and the right image is an interphase nucleus.
- Supplied Product:
- DAPI Counterstain (1500 ng/mL ) 250 uL
- Note:
Hybridization position of the probes on the chromosome.-
- Probe 1:
Size:
Fluorophore:
Location: - p53
Approximately 190kb
Texas Red
17p13.1
- Probe 2:
Size:
Fluorophore:
Location: - CEN17q
Approximately 540kb
FITC
17q11.2
- Probe Gap:
- The gap between two probes is approximately 24,700 kb.
- Origin:
- Human
- Source:
- Genomic DNA
- Regulation Status:
- For research use only (RUO)
- Applications
- Fluorescent In Situ Hybridization (Cell)
- Protocol Download
- Fluorescent In Situ Hybridization (Formalin/PFA-fixed paraffin-embedded sections)
- enlarge this image
- Human stomach carcinoma (FFPE) stained with p53/CEN17q FISH Probe. Human stomach carcinoma showed no p53 gene amplification.
- Protocol Download
- Application Image
- Fluorescent In Situ Hybridization (Cell)
- Fluorescent In Situ Hybridization (Formalin/PFA-fixed paraffin-embedded sections)
- enlarge
- Entrez GeneID:
- 7157
- Gene Name:
- TP53
- Gene Alias:
- FLJ92943,LFS1,TRP53,p53
- Gene Description:
- tumor protein p53
- Gene Ontology:
- Hyperlink
- Gene Summary:
- This gene encodes tumor protein p53, which responds to diverse cellular stresses to regulate target genes that induce cell cycle arrest, apoptosis, senescence, DNA repair, or changes in metabolism. p53 protein is expressed at low level in normal cells and at a high level in a variety of transformed cell lines, where it's believed to contribute to transformation and malignancy. p53 is a DNA-binding protein containing transcription activation, DNA-binding, and oligomerization domains. It is postulated to bind to a p53-binding site and activate expression of downstream genes that inhibit growth and/or invasion, and thus function as a tumor suppressor. Mutants of p53 that frequently occur in a number of different human cancers fail to bind the consensus DNA binding site, and hence cause the loss of tumor suppressor activity. Alterations of this gene occur not only as somatic mutations in human malignancies, but also as germline mutations in some cancer-prone families with Li-Fraumeni syndrome. Multiple p53 variants due to alternative promoters and multiple alternative splicing have been found. These variants encode distinct isoforms, which can regulate p53 transcriptional activity. [provided by RefSeq
- Other Designations:
- p53 antigen,p53 transformation suppressor,p53 tumor suppressor,phosphoprotein p53,transformation-related protein 53
- Interactome
- Gene Pathway
- Amyotrophic lateral sclerosis (ALS)
- Apoptosis
- Basal cell carcinoma
- Bladder cancer
- Cell cycle
- Chronic myeloid leukemia
- Colorectal cancer
- Endometrial cancer
- Glioma
- Huntington's disease
- MAPK signaling pathway
- Melanoma
- Neurotrophin signaling pathway
- Non-small cell lung cancer
- p53 signaling pathway
- Pancreatic cancer
- Pathways in cancer
- Prostate cancer
- Small cell lung cancer
- Thyroid cancer
- Wnt signaling pathway
- Related Disease
- Abortion, Habitual
- Abortion, Spontaneous
- Acquired Hyperostosis Syndrome
- Acute Disease
- Adenocarcinoma
- Adenocarcinoma, Clear Cell
- Adenocarcinoma, Follicular
- Adenocarcinoma, Mucinous
- Adenoma
- Adenoma, Liver Cell
- Adenomatous Polyposis Coli
- Adrenal Cortex Neoplasms
- Albuminuria
- Alcoholism
- Alzheimer Disease
- Alzheimer disease
- Ameloblastoma
- Aneuploidy
- Anoxia