产品详情
产品名称OPA1 Rabbit mAb
克隆号JM81-35
来源种属Recombinant Rabbit
克隆性 Monoclonal antibody
应用WB, ICC/IF, IHC, FC
种属反应性Human;Mouse;Rat
免疫原描述Recombinant protein
标记Unconjugated
别名Dynamin like 120 kDa protein antibody
Dynamin like 120 kDa protein, mitochondrial antibody
Dynamin-like 120 kDa protein, form S1 antibody
FLJ12460 antibody
Juvenile kjer type optic atrophy antibody
KIAA0567 antibody
KJER type antibody
Large GTP binding protein antibody
largeG antibody
MGM1 antibody
Mitochondrial dynamin like 120 kDa protein antibody
Mitochondrial dynamin like GTPase antibody
NPG antibody
NTG antibody
OAK antibody
OPA 1 antibody
opa1 antibody
OPA1 gene antibody
OPA1_HUMAN antibody
Optic atrophy 1 (autosomal dominant) antibody
OPTIC ATROPHY 1 antibody
Optic atrophy 1 gene protein antibody
Optic atrophy 1 homolog (human) antibody
Optic atrophy protein 1 antibody
Optic atrophy protein 1 homolog antibody
数据库入口号Swiss-Prot#:O60313
Uniprot
O60313
计算分子量85 kDa
配方1*TBS (pH7.4), 1%BSA, 40%Glycerol. Preservative: 0.05% Sodium Azide.
保存Store at -20˚C
应用详情
WB: 1:500-1:1000
IHC: 1:50-1:200
ICC: 1:50-1:200
FC: 1:50-1:100
OPA1 is a cause of optic atrophy type 1. OPA1 is mostly expressed in the mitochondrial biogenesis. OPA1 is a cause of optic atrophy type 1. OPA1 is mostly expressed In retina but can also be expressed in brain, testis, heart and skeletal muscles.
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et al,A Novel CYP2E1 Inhibitor, 4‐Methyl‐5‐Acetylthiazole (Q11), Alleviates Obesity Via Modulating Adipose Inflammation and Mitochondrial Dysfunction
, (2025),
PMID:
41420839
Yes
