HADH polyclonal antibody
产品名称： HADH polyclonal antibody
英文名称： HADH polyclonal antibody
产品编号： PAB7412
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:
- Goat polyclonal antibody raised against synthetic peptide of HADH.
- Immunogen:
- A synthetic peptide corresponding to human HADH.
- Sequence:
- C-YERGDASKEDID
- Host:
- Goat
- Theoretical MW (kDa):
- 34.3
- Reactivity:
- Human
- Form:
- Liquid
- Purification:
- Antigen affinity purification
- Concentration:
- 0.5 mg/mL
- Storage Buffer:
- In Tris saline, pH 7.3 (0.5% BSA, 0.02% sodium azide)
- Storage Instruction:
- Store at -20°C.
Aliquot to avoid repeated freezing and thawing.
- Quality Control Testing:
- Antibody Reactive Against Synthetic Peptide.
- Recommend Usage:
- ELISA (1:64000)
Western Blot (0.01-0.03 ug/mL)
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.
- Familial hyperinsulinemic hypoglycemia caused by a defect in the SCHAD enzyme of mitochondrial fatty acid oxidation.
Molven A, Matre GE, Duran M, Wanders RJ, Rishaug U, Njolstad PR, Jellum E, Sovik O.Diabetes. 2004 Jan;53(1):221-7.
- Applications
- Western Blot (Tissue lysate)
- HADH polyclonal antibody (Cat # PAB7412) (0.02 ug/mL) staining of human kidney lysate (35 ug protein in RIPA buffer). Primary incubation was 1 hour. Detected by chemiluminescence.
- Entrez GeneID:
- 3033
- Protein Accession#:
- NP_005318.2
- Gene Name:
- HADH
- Gene Alias:
- HAD,HADH1,HADHSC,HHF4,M/SCHAD,MGC8392,SCHAD
- Gene Description:
- hydroxyacyl-Coenzyme A dehydrogenase
- Gene Ontology:
- Hyperlink
- Gene Summary:
- This gene is a member of the 3-hydroxyacyl-CoA dehydrogenase gene family. The encoded protein functions in the mitochondrial matrix to catalyze the oxidation of straight-chain 3-hydroxyacyl-CoAs as part of the beta-oxidation pathway. Its enzymatic activity is highest with medium-chain-length fatty acids. Mutations in this gene cause one form of familial hyperinsulinemic hypoglycemia. The human genome contains a related pseudogene. [provided by RefSeq
- Other Designations:
- L-3-hydroxyacyl-Coenzyme A dehydrogenase,L-3-hydroxyacyl-Coenzyme A dehydrogenase, short chain