HPGD purified MaxPab mouse polyclonal antibody (B02P)
产品名称： HPGD purified MaxPab mouse polyclonal antibody (B02P)
英文名称： HPGD purified MaxPab mouse polyclonal antibody (B02P)
产品编号： H00003248-B02P
产品价格： null
产品产地： 台湾
品牌商标： Abnova
更新时间： null
使用范围：
亚诺法生技股份有限公司（Abnova)
- 联系人 :
- 地址 : 台湾台北市内湖区洲子街 108 号 9 楼
- 邮编 : 11493
- 所在区域 : 台湾
- 电话 : +886-920**1152 点击查看
- 传真 : 点击查看
- 邮箱 : sales@abnova.com.tw
- Specification
- Product Description:
- Mouse polyclonal antibody raised against a full-length human HPGD protein.
- Immunogen:
- HPGD (NP_000851.2, 1 a.a. ~ 266 a.a) full-length human protein.
- Sequence:
- MHVNGKVALVTGAAQGIGRAFAEALLLKGAKVALVDWNLEAGVQCKAALDEQFEPQKTLFIQCDVADQQQLRDTFRKVVDHFGRLDILVNNAGVNNEKNWEKTLQINLVSVISGTYLGLDYMSKQNGGEGGIIINMSSLAGLMPVAQQPVYCASKHGIVGFTRSAALAANLMNSGVRLNAICPGFVNTAILESIEKEENMGQYIEYKDHIKDMIKYYGILDPPLIANGLITLIEDDALNGAIMKITTSKGIHFQDYDTTPFQAKTQ
- Host:
- Mouse
- Reactivity:
- Human
- Storage Buffer:
- In 1x PBS, pH 7.2
- Storage Instruction:
- Store at -20°C or lower. Aliquot to avoid repeated freezing and thawing.
- Quality Control Testing:
- Antibody reactive against mammalian transfected lysate.
- MSDS:
Download
- Applications
- Western Blot (Tissue lysate)
- HPGD MaxPab polyclonal antibody. Western Blot analysis of HPGD expression in human liver.
- Protocol Download
- Western Blot (Transfected lysate)
- Western Blot analysis of HPGD expression in transfected 293T cell line (H00003248-T02) by HPGD MaxPab polyclonal antibody.
Lane 1: HPGD transfected lysate(29.26 KDa).
Lane 2: Non-transfected lysate. - Protocol Download
- Entrez GeneID:
- 3248
- GeneBank Accession#:
- NM_000860.3
- Protein Accession#:
- NP_000851.2
- Gene Name:
- HPGD
- Gene Alias:
- 15-PGDH,PGDH,PGDH1,SDR36C1
- Gene Description:
- hydroxyprostaglandin dehydrogenase 15-(NAD)
- Omim ID:
- 601688
- Gene Ontology:
- Hyperlink
- Gene Summary:
- 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
- Other Designations:
- 15-hydroxy prostaglandin dehydrogenase,15-hydroxyprostaglandin dehydrogenase,NAD+-dependent 15-hydroxyprostaglandin dehydrogenase,short chain dehydrogenase/reductase family 36C, member 1
- Related Disease
- Adenoma
- Alzheimer Disease
- Alzheimer disease
- Amyotrophic Lateral Sclerosis
- Amyotrophic lateral sclerosis
- Cardiovascular Diseases
- Chorioamnionitis
- Colorectal Neoplasms
- Diabetes Complications
- Diabetes Mellitus, Type 2
- Ductus Arteriosus, Patent
- Edema
- Fetal Membranes, Premature Rupture
- Genetic Predisposition to Disease
- Infant, Premature, Diseases
- Lung Neoplasms
- Metabolic Syndrome X
- Neoplasms
- Obstetric Labor, Premature