联系我们

400-8787-807

快速订购

LAL Mouse mAb

-YM0410

2
主要信息
Target

LAL

Host Species

Mouse

Reactivity

Human

Applications

WB, ELISA

MW

45kD (Calculated)

Conjugate/Modification

Unmodified

货号: YM0410
规格
价格
货期
数量
200μL
¥5,880.00
一周

0

100μL
¥3,200.00
一周

0

50μL
¥2,000.00
一周

0

加入购物车

已收藏

收藏

定制服务咨询
详细信息
推荐稀释比
WB 1:500-1:2000; ELISA 1:10000; Not yet tested in other applications.
组成
Liquid in PBS containing 50% glycerol, 0.5% BSA and 0.02% sodium azide.
特异性
LAL Monoclonal Antibody detects endogenous levels of LAL protein.
纯化工艺
Affinity purification
储存
-15°C to -25°C/1 year(Do not lower than -25°C)
理论分子量
45kD
修饰
Unmodified
克隆性
Monoclonal
相关产品
Secondary Antibodies
Goat Anti Mouse IgG(H+L) (HRP)
RS0001

预览→

Secondary Antibodies
Goat Anti Rabbit IgG(H+L) (HRP)
RS0002

预览→

Primary Antibodies
β-actin (PTR2364) Mouse mAb
YM3028

预览→

Primary Antibodies
GAPDH (PTR2304) Mouse mAb
YM3029

预览→

抗原&靶点信息
免疫原:
Purified recombinant fragment of LAL expressed in E. Coli.
展开内容
特异性:
LAL Monoclonal Antibody detects endogenous levels of LAL protein.
展开内容
基因名称:
LIPA
展开内容
蛋白名称:
Lysosomal acid lipase/cholesteryl ester hydrolase
展开内容
别名:
LIPA ;
Lysosomal acid lipase/cholesteryl ester hydrolase ;
Acid cholesteryl ester hydrolase ;
LAL ;
Cholesteryl esterase ;
Lipase A ;
Sterol esterase
展开内容
数据库链接:
Organism 基因 ID SwissProt
Human 3988; P38571;
Mouse Q9Z0M5;
背景:
This gene encodes lipase A, the lysosomal acid lipase (also known as cholesterol ester hydrolase). This enzyme functions in the lysosome to catalyze the hydrolysis of cholesteryl esters and triglycerides. Mutations in this gene can result in Wolman disease and cholesteryl ester storage disease. Alternatively spliced transcript variants have been found for this gene. [provided by RefSeq, Jan 2014],
展开内容
功能:
Catalytic activity:A steryl ester + H(2)O = a sterol + a fatty acid.,Disease:Defects in LIPA are the cause of cholesteryl ester storage disease (CESD) [MIM:278000]. CESD is a mild manifestation of LIPA deficiency, leading to the accumulation of cholesteryl esters and triglycerides in most tissues of the body. It is characterized by late-onset.,Disease:Defects in LIPA are the cause of Wolman disease (WOD) [MIM:278000]. WOD is a severe manifestation of LIPA deficiency, leading to the accumulation of cholesteryl esters and triglycerides in most tissues of the body. WOD occurs in infancy and is nearly always fatal before the age of 1 year.,Function:Crucial for the intracellular hydrolysis of cholesteryl esters and triglycerides that have been internalized via receptor-mediated endocytosis of lipoprotein particles. Important in mediating the effect of LDL (low density lipoprotein) uptake on suppression of hydroxymethylglutaryl-CoA reductase and activation of endogenous cellular cholesteryl ester formation.,similarity:Belongs to the AB hydrolase superfamily. Lipase family.,
展开内容
细胞定位:
Lysosome .
展开内容
组织表达:
Most abundantly expressed in brain, lung, kidney and mammary gland, a moderate expression seen in placenta and expressed at low levels in the liver and heart.
展开内容
研究领域:
>>Steroid biosynthesis ;
>>Lysosome ;
>>Cholesterol metabolism
展开内容
货号: YM0410
规格
价格
货期
数量
200μL
¥5,880.00
一周

0

100μL
¥3,200.00
一周

0

50μL
¥2,000.00
一周

0

加入购物车

已收藏

收藏

定制服务咨询

Toggle night Mode

{{pinfoXq.title || ''}}

Catalog: {{pinfoXq.catalog || ''}}
Filter:

All

{{item.name}}

{{pinfo.title}}
-{{pinfo.catalog}}

筛选器:

{{item.descr}}

主要信息
Target
{{pinfo.target}}
Reactivity
{{pinfo.react}}
Applications
{{pinfo.applicat}}
Conjugate/Modification
{{pinfo.coupling}}/{{pinfo.modific}}
MW (kDa)
{{pinfo.mwcalc}}
Host Species
{{pinfo.hostspec}}
Isotype
{{pinfo.isotype}}
查看产品详情
产品 {{index}}/{{pcount}}
上一个产品
下一个产品

{{pvTitle}}

滚轮缩放图片
{{pvDescr}}