HNMT purified MaxPab rabbit polyclonal antibody (D01P)
產品名稱: HNMT purified MaxPab rabbit polyclonal antibody (D01P)
英文名稱: HNMT purified MaxPab rabbit polyclonal antibody (D01P)
產品編號: H00003176-D01P
產品價格: null
產品產地: 臺灣
品牌商標: Abnova
更新時間: null
使用范圍:
亞諾法生技股份有限公司(Abnova)
- 聯系人 :
- 地址 : 臺灣臺北市內湖區洲子街 108 號 9 樓
- 郵編 : 11493
- 所在區域 : 臺灣
- 電話 : +886-920**1152 點擊查看
- 傳真 : 點擊查看
- 郵箱 : sales@abnova.com.tw
- Specification
- Product Description:
- Rabbit polyclonal antibody raised against a full-length human HNMT protein.
- Immunogen:
- HNMT (AAH20677.1, 1 a.a. ~ 292 a.a) full-length human protein.
- Sequence:
- MASSMRSLFSDHGKYVESFRRFLNHSTEHQCMQEFMDKKLPGIIGRIGDTKSEIKILSIGGGAGEIDLQILSKVQAQYPGVCINNEVVEPSAEQIAKYKELVAKTSNLENVKFAWHKETSSEYQSRMLEKKELQKWDFIHMIQMLYYVKDIPATLKFFHSLLGTNAKMLIIVVSGSSGWDKLWKKYGSRFPQDDLCQYITSDDLTQMLDNLGLKYECYDLLSTMDISDCFIDGDENGDLLWDFLTETCNFNATAPPDLRAELGKDLQEPEFSAKKEGKVLFNNTLSFIVIEA
- Host:
- Rabbit
- 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 (Transfected lysate)

- Western Blot analysis of HNMT expression in transfected 293T cell line (H00003176-T01) by HNMT MaxPab polyclonal antibody.
Lane 1: HNMT transfected lysate(33.30 KDa).
Lane 2: Non-transfected lysate. - Protocol Download
- Entrez GeneID:
- 3176
- GeneBank Accession#:
- BC020677.1
- Protein Accession#:
- AAH20677.1
- Gene Name:
- HNMT
- Gene Alias:
- HMT,HNMT-S1,HNMT-S2
- Gene Description:
- histamine N-methyltransferase
- Gene Ontology:
- Hyperlink
- Gene Summary:
- In mammals, histamine is metabolized by two major pathways: N(tau)-methylation via histamine N-methyltransferase and oxidative deamination via diamine oxidase. This gene encodes the first enzyme which is found in the cytosol and uses S-adenosyl-L-methionine as the methyl donor. In the mammalian brain, the neurotransmitter activity of histamine is controlled by N(tau)-methylation as diamine oxidase is not found in the central nervous system. A common genetic polymorphism affects the activity levels of this gene product in red blood cells. Multiple alternatively spliced transcript variants that encode different proteins have been found for this gene. [provided by RefSeq
- Other Designations:
- -
- Gene Pathway
- Related Disease
- Alcoholism
- Angioneurotic Edema
- Asthma
- Asthma
- Attention Deficit Disorder with Hyperactivity
- Bronchial Hyperreactivity
- Bronchiolitis, Viral
- Chronic Disease
- Cognition
- Colitis, Ulcerative
- Dermatitis, Atopic
- Disease Progression
- Duodenal Ulcer
- Essential Tremor
- Essential tremor
- Genetic Predisposition to Disease
- Hearing Loss
- Hypercholesterolemia
- Hypersensitivity, Immediate
