GJB2 FISH Probe
产品名称: GJB2 FISH Probe
英文名称: GJB2 FISH Probe
产品编号: FA0317
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:
- 2706
- Gene Name:
- GJB2
- Gene Alias:
- CX26,DFNA3,DFNB1,HID,KID,NSRD1,PPK
- Gene Description:
- gap junction protein, beta 2, 26kDa
- Gene Ontology:
- Hyperlink
- Gene Summary:
- This gene encodes a member of the gap junction protein family. The gap junctions were first characterized by electron microscopy as regionally specialized structures on plasma membranes of contacting adherent cells. These structures were shown to consist of cell-to-cell channels that facilitate the transfer of ions and small molecules between cells. The gap junction proteins, also known as connexins, purified from fractions of enriched gap junctions from different tissues differ. According to sequence similarities at the nucleotide and amino acid levels, the gap junction proteins are divided into two categories, alpha and beta. Mutations in this gene are responsible for as much as 50% of pre-lingual, recessive deafness. [provided by RefSeq
- Other Designations:
- OTTHUMP00000018093,OTTHUMP00000018094,connexin 26,gap junction protein beta 2,gap junction protein, beta 2, 26kD (connexin 26)
- Related Disease
- Aminoglycoside-induced deafness
- Apraxias
- Attention Deficit Disorder with Hyperactivity
- Auditory Perception
- Auditory Threshold
- Cholesteatoma
- Chorioamnionitis
- Chromosome Aberrations
- Chromosome Deletion
- Chronic Disease
- Cleft Lip
- Cleft Palate
- Cognition
- Cytomegalovirus Infections
- Deafness
- Deafness
- Disease Progression
- Diseases in Twins
- Fetal Membranes, Premature Rupture