HSPD1 monoclonal antibody, clone 1G1
产品名称： HSPD1 monoclonal antibody, clone 1G1
英文名称： HSPD1 monoclonal antibody, clone 1G1
产品编号： MAB2971
产品价格： null
产品产地： 台湾
品牌商标： Abnova
更新时间： null
使用范围：
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:
- Mouse monoclonal antibody raised against recombinant HSPD1.
- Immunogen:
- Recombinant protein corresponding to human HSPD1.
- Host:
- Mouse
- Reactivity:
- Human
- Specificity:
- This antibody recognizes human and other mammalian HSPD1.
- Form:
- Liquid
- Isotype:
- IgG2a
- Storage Buffer:
- In PBS, pH 7.4 (0.1% sodium azide)
- Storage Instruction:
- Store at 4°C.
- Recommend Usage:
- The optimal working dilution should be determined by the end user.
- Note:
- This product contains sodium azide: a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.
- Application Image
- Western Blot
- Immunohistochemistry
- ELISA
- Entrez GeneID:
- 3329
- Gene Name:
- HSPD1
- Gene Alias:
- CPN60,GROEL,HLD4,HSP60,HSP65,HuCHA60,SPG13
- Gene Description:
- heat shock 60kDa protein 1 (chaperonin)
- Gene Ontology:
- Hyperlink
- Gene Summary:
- This gene encodes a member of the chaperonin family. The encoded mitochondrial protein may function as a signaling molecule in the innate immune system. This protein is essential for the folding and assembly of newly imported proteins in the mitochondria. This gene is adjacent to a related family member and the region between the 2 genes functions as a bidirectional promoter. Two pseudogenes, both located on chromosome 8, have been associated with this gene. Two transcript variants encoding the same protein have been identified for this gene. Mutations associated with this gene cause autosomal recessive spastic paraplegia 13. [provided by RefSeq
- Other Designations:
- P60 lymphocyte protein,chaperonin,heat shock 60kD protein 1 (chaperonin),heat shock protein 65,mitochondrial heat shock 60kD protein 1 variant 1,mitochondrial matrix protein P1,short heat shock protein 60 Hsp60s1,spastic paraplegia 13 (autosomal dominant)
- Gene Pathway
- Related Disease