MEIS1 FISH Probe
产品名称: MEIS1 FISH Probe
英文名称: MEIS1 FISH Probe
产品编号: FA0068
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:
- Made to order FISH probes for identification of gene amplification using Fluorescent In Situ Hybridization Technique. (Technology)
- Storage Instruction:
- Store at 4°C in the dark.
- Supplied Product:
- DAPI Counterstain (1500 ng/mL ) 250 uL
- Origin:
- Human
- Source:
- Genomic DNA
- Regulation Status:
- For research use only (RUO)
- Applications
- Fluorescent In Situ Hybridization (Cell)
- Protocol Download
- Application Image
- Fluorescent In Situ Hybridization (Cell)
- Entrez GeneID:
- 4211
- Gene Name:
- MEIS1
- Gene Alias:
- MGC43380
- Gene Description:
- Meis homeobox 1
- Omim ID:
- 601739
- Gene Ontology:
- Hyperlink
- Gene Summary:
- Homeobox genes, of which the most well-characterized category is represented by the HOX genes, play a crucial role in normal development. In addition, several homeoproteins are involved in neoplasia. This gene encodes a homeobox protein belonging to the TALE ('three amino acid loop extension') family of homeodomain-containing proteins. [provided by RefSeq
- Other Designations:
- Meis1, myeloid ecotropic viral integration site 1 homolog,WUGSC:H_NH0444B04.1,leukemogenic homolog protein
- Related Disease
- Atrial Fibrillation
- Attention Deficit Disorder with Hyperactivity
- Cardiovascular Diseases
- Celiac Disease
- Diabetes Mellitus, Type 2
- Edema
- Genetic Predisposition to Disease
- Neuropsychological Tests
- Nocturnal Myoclonus Syndrome
- Obsessive-Compulsive Disorder
- Restless Legs Syndrome
- Tobacco Use Disorder
- Tourette Syndrome