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PERQ2 Rabbit Polyclonal Antibody

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产品基本信息

产品货号
BD-PN2493
产品名称
PERQ2 Rabbit Polyclonal Antibody
类别
常规抗体
基因名称
GIGYF2 KIAA0642 PERQ2 TNRC15
蛋白名称
PERQ amino acid-rich with GYF domain-containing protein 2 (GRB10-interacting GYF protein 2) (Trinucleotide repeat-containing gene 15 protein)
推荐应用
WB
反应种属
Human,Mouse
浓度
1 mg/ml
存储缓冲液
Liquid in PBS containing 50% glycerol, and 0.02% New type preservative N.
Human Gene ID
26058
Human Swissprot No.
Q6Y7W6
Human Swissprot Link
https://www.uniprot.org/uniprotkb/Q6Y7W6/entry
Mouse Swissprot No.
Q6Y7W8
Mouse Swissprot Link
http://www.uniprot.org/uniprot/Q6Y7W8
免疫原
Synthesized peptide derived from human protein . at AA range: 1071-1120
特异性
PERQ2 Polyclonal Antibody detects endogenous levels of protein.
稀释度
WB 1:500-2000 ELISA 1:5000-20000
预测分子量
142kD
运输及保存条件
-20°C/1 year
宿主
Polyclonal, Rabbit,IgG
背景介绍
GRB10 interacting GYF protein 2(GIGYF2) Homo sapiens This gene contains CAG trinucleotide repeats and encodes a protein containing several stretches of polyglutamine residues. The encoded protein may be involved in the regulation of tyrosine kinase receptor signaling. This gene is located in a chromosomal region that was genetically linked to Parkinson disease type 11, and mutations in this gene were thought to be causative for this disease. However, more recent studies in different populations have been unable to replicate this association. Alternative splicing results in multiple transcript variants. [provided by RefSeq, May 2013],
组织表达
Brain,Clones donated by Kazusa DNA Research Inst.,Epithelium,Fetal kidney,K
细胞定位
cell-cell adherens junction,membrane,
功能
disease:Defects in GIGYF2 are the cause of Parkinson disease type 11 (PARK11) [MIM:607688]. Parkinson disease (PD) is a complex, multifactorial disorder that typically manifests after the age of 50 years, although early-onset cases (before 50 years) are known. PD generally arises as a sporadic condition but is occasionally inherited as a simple mendelian trait. Although sporadic and familial PD are very similar, inherited forms of the disease usually begin at earlier ages and are associated with atypical clinical features. PD is characterized by bradykinesia, resting tremor, muscular rigidity and postural instability, as well as by a clinically significant response to treatment with levodopa. The pathology involves the loss of dopaminergic neurons in the substantia nigra and the presence of Lewy bodies (intraneuronal accumulations of aggregated proteins), in surviving neurons in various areas of the brain. PARK11 may show age-dependent penetrance or reduced penetrance.,function:May act cooperatively with GRB10 to regulate tyrosine kinase receptor signaling, including IGF1 and insulin receptors.,sequence caution:Unlikely isoform.,similarity:Belongs to the PERQ family.,similarity:Contains 1 GYF domain.,subunit:Interacts with GRB10.,
期货
现货
纯化
The antibody was affinity-purified from rabbit antiserum by affinity-chromatography using epitope-specific immunogen.

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