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SPG7 mouse monoclonal antibody, clone OTI1C1 (formerly 1C1)
货号: GAM615535
SPG7 mouse monoclonal antibody, clone OTI1C1 (formerly 1C1)
反应种属:
DogHumanMonkeyMouseRat
应用:
FCIFWB
¥ 960
/ 50μl
库存充足
50μl100μl
产品详情
推荐稀释比
产品特性
反应种属
DogHumanMonkeyMouseRat
应用
FCIFWB
纯化方式
Affinity Purification
克隆号
OTI1C1
免疫源
Human recombinant protein fragment corresponding to amino acids 300-573 of human SPG7(NP_003110) produced in E.coli.
来源
Mouse
克隆性
Monoclonal
Background
This gene encodes a nuclear-encoded mitochondrial metalloprotease protein that is a member of the AAA (ATPases associated with a variety of cellular activities) protein family. Members of this protein family share an ATPase domain and have roles in diverse cellular processes including membrane trafficking, intracellular motility, organelle biogenesis, protein folding, and proteolysis. Two transcript variants encoding distinct isoforms have been identified for this gene. Mutations associated with this gene cause autosomal recessive spastic paraplegia 7. [provided by RefSeq]
预测分子量
88.1 kDa
Uniprot
Q9UQ90
Isotype
IgG1
产品别名
SPG7
Anti-SPG7 mouse monoclonal antibody (GAM615535) immunofluorescent staining of COS7 cells transiently transfected by pCMV6-ENTRY SPG7
货号: GAM615535
SPG7 mouse monoclonal antibody, clone OTI1C1 (formerly 1C1)
反应种属:
DogHumanMonkeyMouseRat
应用:
FCIFWB
¥ 960
/ 50μl
库存充足
50μl100μl
产品详情
推荐稀释比
产品特性
反应种属
DogHumanMonkeyMouseRat
应用
FCIFWB
纯化方式
Affinity Purification
克隆号
OTI1C1
免疫源
Human recombinant protein fragment corresponding to amino acids 300-573 of human SPG7(NP_003110) produced in E.coli.
来源
Mouse
克隆性
Monoclonal
Background
This gene encodes a nuclear-encoded mitochondrial metalloprotease protein that is a member of the AAA (ATPases associated with a variety of cellular activities) protein family. Members of this protein family share an ATPase domain and have roles in diverse cellular processes including membrane trafficking, intracellular motility, organelle biogenesis, protein folding, and proteolysis. Two transcript variants encoding distinct isoforms have been identified for this gene. Mutations associated with this gene cause autosomal recessive spastic paraplegia 7. [provided by RefSeq]
预测分子量
88.1 kDa
Uniprot
Q9UQ90
Isotype
IgG1
产品别名
SPG7
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