联系我们

400-8787-807

快速订购

SARDH Rabbit pAb

-YT7522

2 5
主要信息
Target

SARDH

Host Species

Rabbit

Reactivity

Human, Mouse, Rat

Applications

WB, ELISA, IHC

MW

101kD (Calculated)

Conjugate/Modification

Unmodified

货号: YT7522
规格
价格
货期
数量
200μL
¥3,780.00
现货

0

100μL
¥2,300.00
现货

0

40μL
¥960.00
现货

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 1:500-2000; IHC 1:50-300; ELISA 1:2000-20000
组成
Liquid in PBS containing 50% glycerol, 0.5% BSA and 0.02% sodium azide.
特异性
This antibody detects endogenous levels of SARDH at Human/Mouse/Rat
纯化工艺
The antibody was affinity-purified from rabbit antiserum by affinity-chromatography using epitope-specific immunogen.
储存
-15°C to -25°C/1 year(Do not lower than -25°C)
浓度
1 mg/ml
理论分子量
101kD
修饰
Unmodified
克隆性
Polyclonal
同种型
IgG
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:
Synthesized peptide derived from human SARDH AA range: 279-329
展开内容
特异性:
This antibody detects endogenous levels of SARDH at Human/Mouse/Rat
展开内容
基因名称:
SARDH DMGDHL1
展开内容
蛋白名称:
SARDH
展开内容
数据库链接:
Organism 基因 ID SwissProt
Human 1757; Q9UL12;
Mouse 192166; Q99LB7;
Rat 114123; Q64380;
背景:
This gene encodes an enzyme localized to the mitochondrial matrix which catalyzes the oxidative demethylation of sarcosine. This enzyme is distinct from another mitochondrial matrix enzyme, dimethylglycine dehydrogenase, which catalyzes a reaction resulting in the formation of sarcosine. Mutations in this gene are associated with sarcosinemia. Alternatively spliced transcript variants have been described. [provided by RefSeq, Oct 2008],
展开内容
功能:
Catalytic activity:Sarcosine + acceptor + H(2)O = glycine + formaldehyde + reduced acceptor.,cofactor:Binds 1 FAD covalently per monomer.,Disease:Defects in SARDH are a ause of sarcosinemia [MIM:268900]. Sarcosinemia is a metabolic disorder characterized by an increased concentration of sarcosine in plasma and urine due to sarcosine dehydrogenase deficiency. Prevalence has been estimated at 1:28'000 to 1:350'000 in newborn screening programs. Sarcosinemia is most probably a benign condition without significant clinical problems. It is transmitted in an autosomal recessive manner.,pathway:Amine and polyamine degradation; sarcosine degradation; formaldehyde and glycine from sarcosine: step 1/1.,similarity:Belongs to the gcvT family.,
展开内容
细胞定位:
Mitochondrion matrix .
展开内容
组织表达:
Expressed in pancreas, liver and kidney.
展开内容
研究领域:
>>Glycine, serine and threonine metabolism ;
>>Metabolic pathways
展开内容
货号: YT7522
规格
价格
货期
数量
200μL
¥3,780.00
现货

0

100μL
¥2,300.00
现货

0

40μL
¥960.00
现货

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}}