TUPLE1/ARSA FISH Probe
产品名称: TUPLE1/ARSA FISH Probe
英文名称: TUPLE1/ARSA FISH Probe
产品编号: FA0654
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 (150 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:
- 7290
- Gene Name:
- HIRA
- Gene Alias:
- DGCR1,TUP1,TUPLE1
- Gene Description:
- HIR histone cell cycle regulation defective homolog A (S. cerevisiae)
- Omim ID:
- 600237
- Gene Ontology:
- Hyperlink
- Gene Summary:
- This gene encodes a histone chaperone that preferentially places the variant histone H3.3 in nucleosomes. Orthologs of this gene in yeast, flies, and plants are necessary for the formation of transcriptionally silent heterochomatin. This gene plays an important role in the formation of the senescence-associated heterochromatin foci. These foci likely mediate the irreversible cell cycle changes that occur in senescent cells. It is considered the primary candidate gene in some haploinsufficiency syndromes such as DiGeorge syndrome, and insufficient production of the gene may disrupt normal embryonic development. [provided by RefSeq
- Other Designations:
- DiGeorge critical region gene 1,HIR histone cell cycle regulation defective homolog A
- Entrez GeneID:
- 410
- Gene Name:
- ARSA
- Gene Alias:
- MLD
- Gene Description:
- arylsulfatase A
- Gene Ontology:
- Hyperlink
- Gene Summary:
- The protein encoded by this gene hydrolyzes cerebroside sulfate to cerebroside and sulfate. Defects in this gene lead to metachromatic leucodystrophy (MLD), a progressive demyelination disease which results in a variety of neurological symptoms and ultimately death. Multiple alternatively spliced transcript variants, one of which encodes a distinct protein, have been described for this gene. [provided by RefSeq
- Other Designations:
- OTTHUMP00000196546,OTTHUMP00000196548