MVK polyclonal antibody (A01)
產品名稱: MVK polyclonal antibody (A01)
英文名稱: MVK polyclonal antibody (A01)
產品編號: H00004598-A01
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:
- Mouse polyclonal antibody raised against a partial recombinant MVK.
- Immunogen:
- MVK (AAH16140, 297 a.a. ~ 396 a.a) partial recombinant protein with GST tag.
- Sequence:
- LIDMNQHHLNALGVGHASLDQLCQVTRARGLHSKLTGAGGGGCGITLLKPGLEQPEVEATKQALTSCGFDCLETSIGAPGVSIHSATSLDSRVQQALDGL
- Host:
- Mouse
- Reactivity:
- Human, Mouse
- Storage Buffer:
- 50 % glycerol
- Storage Instruction:
- Store at -20°C or lower. Aliquot to avoid repeated freezing and thawing.
- Quality Control Testing:
- Antibody Reactive Against Recombinant Protein.

Western Blot detection against Immunogen (37.11 KDa) .
- MSDS:
Download
- Applications
- Western Blot (Cell lysate)

- MVK polyclonal antibody (A01), Lot # 051116JC01 Western Blot analysis of MVK expression in A-431 ( Cat # L015V1 ).
- Protocol Download
- Western Blot (Cell lysate)

- MVK polyclonal antibody (A01), Lot # 051116JC01. Western Blot analysis of MVK expression in NIH/3T3.
- Protocol Download
- Western Blot (Recombinant protein)
- Protocol Download
- Entrez GeneID:
- 4598
- GeneBank Accession#:
- BC016140
- Protein Accession#:
- AAH16140
- Gene Name:
- MVK
- Gene Alias:
- FLJ96772,LRBP,MK,MVLK
- Gene Description:
- mevalonate kinase
- Gene Ontology:
- Hyperlink
- Gene Summary:
- This gene encodes the peroxisomal enzyme mevalonate kinase. Mevalonate is a key intermediate, and mevalonate kinase a key early enzyme, in isoprenoid and sterol synthesis. Mevalonate kinase deficiency caused by mutation of this gene results in mevalonic aciduria, a disease characterized psychomotor retardation, failure to thrive, hepatosplenomegaly, anemia and recurrent febrile crises. Defects in this gene also cause hyperimmunoglobulinaemia D and periodic fever syndrome, a disorder characterized by recurrent episodes of fever associated with lymphadenopathy, arthralgia, gastrointestinal dismay and skin rash. Two transcript variants that encode the same protein have been found for this gene. [provided by RefSeq
- Other Designations:
- LH receptor mRNA-binding protein,mevalonic aciduria
- Related Disease
- Amyloidosis
- Autoimmune Diseases
- Behcet Syndrome
- Coronary Artery Disease
- Crohn's disease
- Diabetes Mellitus, Type 2
- Diarrhea
- Dyslipidemias
- Familial Mediterranean Fever
- Familial Mediterranean fever
- Genetic Predisposition to Disease
- Hyperlipidemias
- Hypertriglyceridemia
- Inflammation
- Irritable Bowel Syndrome
- Narcolepsy
- Pain
- Stomatitis, Aphthous
- Syndrome
