PEMT (C-term) Peptide
产品名称: PEMT (C-term) Peptide
英文名称: PEMT (C-term) Peptide
产品编号: P0163
产品价格: 0
产品产地: 台湾
品牌商标: Abnova
更新时间: null
使用范围: null
亚诺法生技股份有限公司(Abnova)
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- 所在区域 : 台湾
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- Specification
- Product Description:
- Rabbit polyclonal antibody raised against synthetic peptide of PEMT.
- Immunogen:
- A synthetic peptide (conjugated with KLH) corresponding to C-terminus of human PEMT.
- Host:
- Rabbit
- Reactivity:
- Human
- Form:
- Liquid
- Purification:
- Protein A purification
- Storage Buffer:
- In PBS (0.09% sodium azide)
- Storage Instruction:
- Store at 4°C. For long term storage store at -20°C.
Aliquot to avoid repeated freezing and thawing.
- Recommend Usage:
- ELISA (1:1000)
Western Blot (1:50-100)
The optimal working dilution should be determined by the end user.
- Note:
- This product contains sodium azide: a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.
- Publication Reference
- 1.
- Structure, expression profile and alternative processing of the human phosphatidylethanolamine N-methyltransferase (PEMT) gene.
Shields DJ, Agellon LB, Vance DE.Biochim Biophys Acta. 2001 May 31;1532(1-2):105-14.
- 2.
- Gene expression profiling in the human hypothalamus-pituitary-adrenal axis and full-length cDNA cloning.
Hu RM, Han ZG, Song HD, Peng YD, Huang QH, Ren SX, Gu YJ, Huang CH, Li YB, Jiang CL, Fu G, Zhang QH, Gu BW, Dai M, Mao YF, Gao GF, Rong R, Ye M, Zhou J, Xu SH, Gu J, Shi JX, Jin WR, Zhang CK, Wu TM, Huang GY, Chen Z, Chen MD, Chen JL.Proc Natl Acad Sci U S A. 2000 Aug 15;97(17):9543-8.
- 3.
- Identification of three novel cDNAs for human phosphatidylethanolamine N-methyltransferase and localization of the human gene on chromosome 17p11.2.
Walkey CJ, Shields DJ, Vance DE.Biochim Biophys Acta. 1999 Jan 4;1436(3):405-12.
- Entrez GeneID:
- 10400
- Protein Accession#:
- NP_009100;Q9UBM1
- Gene Name:
- PEMT
- Gene Alias:
- MGC2483,PEAMT,PEMPT,PEMT2,PNMT
- Gene Description:
- phosphatidylethanolamine N-methyltransferase
- Omim ID:
- 602391
- Gene Ontology:
- Hyperlink
- Gene Summary:
- This gene encodes an enzyme which converts phosphatidylethanolamine to phosphatidylcholine by sequential methylation in the liver. The protein localizes to the endoplasmic reticulum and mitochondria-associated membranes. The gene is within the Smith-Magenis syndrome region on chromosome 17. Alternate splicing of this gene results in three transcript variants encoding two different isoforms. [provided by RefSeq
- Other Designations:
- OTTHUMP00000065536,OTTHUMP00000065537
- Gene Pathway
- Related Disease
- Breast cancer
- Breast Neoplasms
- Cardiovascular Diseases
- Choline Deficiency
- Cleft Lip
- Cleft Palate
- Coronary Artery Disease
- Diabetes Mellitus, Type 2
- Edema
- Fatty Liver
- Fatty Liver, Alcoholic
- Folic Acid Deficiency
- Genetic Predisposition to Disease
- Metabolic Syndrome X
- Obesity
- Obesity, Abdominal
- Schizophrenia
- Schizophrenia
- Tobacco Use Disorder