ACAT1 (Human) Recombinant Protein (P01)
产品名称: ACAT1 (Human) Recombinant Protein (P01)
英文名称: ACAT1 (Human) Recombinant Protein (P01)
产品编号: H00000038-P01
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)
- 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:
- Human ACAT1 full-length ORF ( AAH10942, 16 a.a. - 162 a.a.) recombinant protein with GST-tag at N-terminal.
- Sequence:
- SPLLRRLVQEIRYVERSYVSKPTLKEVVIVSATRTPIGSFLGSLSLLPATKLGSIAIQGAIEKAGIPKEEVKEAYMGNVLQGGEGQAPTRQAVLGAGLPISTPCTTINKVCASGMKAIMMASQSLMCGHQIKQETGSLAKICCHVKR
- Theoretical MW (kDa):
- 41.91
- Preparation Method:
- in vitro wheat germ expression system
- Purification:
- Glutathione Sepharose 4 Fast Flow
- Storage Buffer:
- 50 mM Tris-HCI, 10 mM reduced Glutathione, pH=8.0 in the elution buffer.
- Storage Instruction:
- Store at -80°C. Aliquot to avoid repeated freezing and thawing.
- Quality Control Testing:
- 12.5% SDS-PAGE Stained with Coomassie Blue.
- Note:
- Best use within three months from the date of receipt of this protein.
- MSDS:
- Download
- Application Image
- Enzyme-linked Immunoabsorbent Assay
- Western Blot (Recombinant protein)
- Antibody Production
- Protein Array
- Entrez GeneID:
- 38
- GeneBank Accession#:
- BC010942
- Protein Accession#:
- AAH10942
- Gene Name:
- ACAT1
- Gene Alias:
- ACAT,MAT,T2,THIL
- Gene Description:
- acetyl-Coenzyme A acetyltransferase 1
- Gene Ontology:
- Hyperlink
- Gene Summary:
- This gene encodes a mitochondrially localized enzyme that catalyzes the reversible formation of acetoacetyl-CoA from two molecules of acetyl-CoA. Defects in this gene are associated with 3-ketothiolase deficiency, an inborn error of isoleucine catabolism characterized by urinary excretion of 2-methyl-3-hydroxybutyric acid, 2-methylacetoacetic acid, tiglylglycine, and butanone. [provided by RefSeq
- Other Designations:
- acetoacetyl Coenzyme A thiolase
- Gene Pathway
- Related Disease
- Alzheimer Disease
- Alzheimer disease
- Amino Acid Metabolism, Inborn Errors
- Atherosclerosis
- Cardiovascular Diseases
- Dementia
- Diabetes Complications
- Drug Toxicity
- Edema
- Genetic Predisposition to Disease
- Hypercholesterolemia
- Hyperlipidemias
- Hypertriglyceridemia
- Metabolic Syndrome X
- Neoplasms
- Osteoporosis