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PGDH Rabbit Polyclonal Antibody

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产品基本信息

产品货号
BD-PN4052
产品名称
PGDH Rabbit Polyclonal Antibody
类别
常规抗体
基因名称
HPGD PGDH1
蛋白名称
PGDH
推荐应用
WB
反应种属
Human,Mouse,Rat
浓度
1 mg/ml
存储缓冲液
Liquid in PBS containing 50% glycerol, 0.5% BSA and 0.02% New type preservative N.
Human Gene ID
3248
Human Gene Link
https://www.uniprot.org/uniprot/3248
Human Swissprot No.
P15428
Human Swissprot Link
https://www.uniprot.org/uniprotkb/P15428/entry
Mouse Gene ID
15446
Mouse Gene Link
https://www.uniprot.org/uniprot/15446
Mouse Swissprot No.
Q8VCC1
Mouse Swissprot Link
https://www.uniprot.org/uniprotkb/Q8VCC1
Rat Gene ID
79242
Rat Gene Link
https://www.uniprot.org/uniprot/79242
Rat Swissprot No.
O08699
Rat Swissprot Link
https://www.uniprot.org/uniprotkb/O08699
免疫原
Synthesized peptide derived from human PGDH AA range: 192-242
特异性
This antibody detects endogenous levels of PGDH at Human/Mouse/Rat
稀释度
WB 1:500-2000
参考分子量
29kD
运输及保存条件
-20°C/1 year
宿主
Polyclonal, Rabbit,IgG
背景介绍
This gene encodes a member of the short-chain nonmetalloenzyme alcohol dehydrogenase protein family. The encoded enzyme is responsible for the metabolism of prostaglandins, which function in a variety of physiologic and cellular processes such as inflammation. Mutations in this gene result in primary autosomal recessive hypertrophic osteoarthropathy and cranioosteoarthropathy. Multiple transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Mar 2009],
组织表达
Detected in colon epithelium (at protein level).
细胞定位
Cytoplasm.
功能
catalytic activity:(5Z,13E,15S)-11-alpha,15-dihydroxy-9-oxoprost-5,13-dienoate + NAD(+) = (5Z,13E)-11-alpha-hydroxy-9,15-dioxoprost-5,13-dienoate + NADH.,disease:Defects in HPGD are the cause of cranioosteoarthropathy (COA) [MIM:259100]. Clinical features include infantile onset of swelling of the joints, digital clubbing, hyperhidrosis, delayed closure of the fontanels, periostosis, and variable patent ductus arteriosus. Pachydermia is not a prominent feature.,disease:Defects in HPGD are the cause of primary hypertrophic osteoathropathy autosomal recessive (PHOAR) [MIM:259100]; also known as pachydermoperiostosis autosomal recessive. Primary hypertrophic osteoarthropathy is characterized by digital clubbing, osterarthropathy, variable features of pachydermia, delayed closure of the fontanels, and congenital heart disease.,function:Inactivation of prostaglandins.,similarity:Belongs to the short-chain dehydrogenases/reductases (SDR) family.,subunit:Homodimer.,
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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