FITC标记的P5C还原酶1抗体-抗体-抗体-生物在线
上海沪震实业有限公司
FITC标记的P5C还原酶1抗体

FITC标记的P5C还原酶1抗体

商家询价

产品名称: FITC标记的P5C还原酶1抗体

英文名称: Anti-PYCR1/FITC

产品编号: HZ-

产品价格: null

产品产地: 中国/上海

品牌商标: HZbscience

更新时间: 2023-08-17T10:24:20

使用范围: ICC=1:50-200 IF=1:50-200

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 Rabbit Anti-PYCR1/FITC Conjugated antibody 

FITC标记的P5C还原酶1抗体

 

英文名称 Anti-PYCR1/FITC
中文名称 FITC标记的P5C还原酶1抗体
别    名 P5C; P5C reductase 1; P5C reductase; P5CR 1; P5CR; PIG45; PP222; Proliferation inducing protein 45; PYCR 1; PYCR; Pyrroline 5 carboxylate reductase 1; Pyrroline 5 carboxylate reductase 1 mitochondrial.  
规格价格 100ul/2980元 购买        大包装/询价
说 明 书 100ul  
研究领域 肿瘤  细胞生物  发育生物学  信号转导  
抗体来源 Rabbit
克隆类型 Polyclonal
交叉反应 Human, 
产品应用 ICC=1:50-200 IF=1:50-200  
not yet tested in other applications.
optimal dilutions/concentrations should be determined by the end user.
分 子 量 33kDa
性    状 Lyophilized or Liquid
浓    度 1mg/ml
免 疫 原 KLH conjugated synthetic peptide derived from human PYCR1
亚    型 IgG
纯化方法 affinity purified by Protein A
储 存 液 0.01M TBS(pH7.4) with 1% BSA, 0.03% Proclin300 and 50% Glycerol.
保存条件 Store at -20 °C for one year. Avoid repeated freeze/thaw cycles. The lyophilized antibody is stable at room temperature for at least one month and for greater than a year when kept at -20°C. When reconstituted in sterile pH 7.4 0.01M PBS or diluent of antibody the antibody is stable for at least two weeks at 2-4 °C.
产品介绍 background:
This gene encodes an enzyme that catalyzes the NAD(P)H-dependent conversion of pyrroline-5-carboxylate to proline. This enzyme may also play a physiologic role in the generation of NADP(+) in some cell types. The protein forms a homopolymer and localizes to the mitochondrion. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Aug 2013]

Function:
Housekeeping enzyme that catalyzes the last step in proline biosynthesis. Can utilize both NAD and NADP, but has higher affinity for NAD. Involved in the cellular response to oxidative stress.

Subunit:
Homodecamer; composed of 5 homodimers.

Subcellular Location:
Mitochondrial

DISEASE:
The disease is caused by mutations affecting the gene represented in this entry. Disease description:A disorder characterized by an excessive congenital skin wrinkling, a large fontanelle with delayed closure, a typical facial appearance with downslanting palpebral fissures, a general connective tissue weakness, and varying degrees of growth and developmental delay and neurological abnormalities. Patients do not manifest metabolic abnormalities.

Similarity:
Belongs to the pyrroline-5-carboxylate reductase family.

Database links:

Entrez Gene: 5831 Human

Entrez Gene: 209027 Mouse

Entrez Gene: 287877 Rat

Omim: 179035 Human

SwissProt: P32322 Human

SwissProt: Q922W5 Mouse

SwissProt: B2RYR3 Rat



Important Note:
This product as supplied is intended for research use only, not for use in human, therapeutic or diagnostic applications

该基因编码一种酶,该酶催化-5-羧酸盐的NAD(p)H依赖性转化为脯氨酸。这种酶也可能在某些细胞类型中产生NADP(+)的生理作用。蛋白质形成均聚物并定位于线粒体。选择性剪接导致多个转录变体。[ RefSeq,Aug 2013提供]