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AGL (基因名), Glycogen debranching enzyme (蛋白名), gde_human.
产品名称:

Human AGL/ Glycogen debranching enzyme Recombinant Protein
糖原脱支酶

货号:

R15166h

商标:
EIAab®
监管等级:
别名:

Glycogen debrancher, GDE

序列号:
P35573
来源:
E.coli
种属:
Human
标签:
His
序列:
1-230aa
预估分子量:
25.3 kDa (monomer)
纯度:
Greater than 90% by SDS-PAGE
浓度:
Reconstitution Dependent
形态:
Liquid
内毒素水平:
Please contact protein@eiaab.com The technician for more information.
应用:
存储缓冲液:
50mM NaH2PO4, 500mM NaCl Buffer with 500mM Imidazole, 10%glycerol(PH8.0)
存储:
Store at -20°C. (Avoid repeated freezing and thawing.)
研究领域:
-
Human AGL Protein
规格 & 价格: cart
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Human AGL Protein
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产品说明书
数据表: 下载说明书
MSDS: MSDS
在线询价


R&D 技术数据
Human AGL Protein
Recombinant human AGL protein was determined by 12% SDS-PAGE stained with Coomassie Blue under reducing conditions.
基因位点
Cytogenetic band: 1p21.2 by HGNC 1p21.2 by Entrez Gene 1p21.2 by Ensembl
AGL Gene in genomic location: bands according to Ensembl, locations according to GeneLoc (and/or Entrez Gene and/or Ensembl if different)
基因位点
通用注释


亚单元:
Monomer. Interacts with NHLRC1/malin.


功能:
Multifunctional enzyme acting as 1,4-alpha-D-glucan:1,4-alpha-D-glucan 4-alpha-D-glycosyltransferase and amylo-1,6-glucosidase in glycogen degradation.


亚细胞位置:
Cytoplasm Under glycogenolytic conditions localizes to the nucleus.


该产品尚未在任何出版物中被引用。

[1].
"Molecular genetic basis and prevalence of glycogen storage disease type IIIA in the Faroe Islands."

[2].
"Heterogeneous mutations in the glycogen-debranching enzyme gene are responsible for glycogen storage disease type IIIa in Japan."

[3].
"Isolation and nucleotide sequence of human liver glycogen debranching enzyme mRNA: identification of multiple tissue-specific isoforms."

[4].
"A nonsense mutation due to a single base insertion in the 3'-coding region of glycogen debranching enzyme gene associated with a severe phenotype in a patient with glycogen storage disease type IIIa."

[5].
"Human glycogen debranching enzyme gene (AGL): complete structural organization and characterization of the 5' flanking region."

[6].
"A novel donor splice site mutation in the glycogen debranching enzyme gene is associated with glycogen storage disease type III."

[7].
"Mutations in exon 3 of the glycogen debranching enzyme gene are associated with glycogen storage disease type III that is differentially expressed in liver and muscle."

[8].
"Assignment of the human glycogen debrancher gene to chromosome 1p21."

[9].
"Genome-wide association study of lung function decline in adults with and without asthma."

[10].
"Personalized smoking cessation: interactions between nicotine dose, dependence and quit-success genotype score."
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