NTRK1(Texas Red)/CEN1p(FITC) FISH Probe
产品名称: NTRK1(Texas Red)/CEN1p(FITC) FISH Probe
英文名称: NTRK1(Texas Red)/CEN1p(FITC) FISH Probe
产品编号: FA0495
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:
- 4914
- Gene Name:
- NTRK1
- Gene Alias:
- DKFZp781I14186,MTC,TRK,TRK1,TRKA,p140-TrkA
- Gene Description:
- neurotrophic tyrosine kinase, receptor, type 1
- Gene Ontology:
- Hyperlink
- Gene Summary:
- This gene encodes a member of the neurotrophic tyrosine kinase receptor (NTKR) family. This kinase is a membrane-bound receptor that, upon neurotrophin binding, phosphorylates itself and members of the MAPK pathway. The presence of this kinase leads to cell differentiation and may play a role in specifying sensory neuron subtypes. Mutations in this gene have been associated with congenital insensitivity to pain, anhidrosis, self-mutilating behavior, mental retardation and cancer. Alternate transcriptional splice variants of this gene have been found, but only three have been characterized to date. [provided by RefSeq
- Other Designations:
- OTTHUMP00000038736,Oncogene TRK,high affinity nerve growth factor receptor,tyrosine kinase receptor A
- Related Disease
- Alzheimer Disease
- Alzheimer disease
- Asperger Syndrome
- Autistic Disorder
- Cardiovascular Diseases
- Diabetes Mellitus, Type 2
- Disease Models, Animal
- Eating Disorders
- Edema
- Genetic Predisposition to Disease
- Hereditary Sensory and Autonomic Neuropathies
- Hyperparathyroidism, Secondary
- Kidney Failure, Chronic
- Leukemia, Myeloid, Acute
- Mental Disorders
- Neuroblastoma
- Social Perception
- Thyroid Diseases
- Thyroid Neoplasms