Thermo Fisher Scientific LPL Monoclonal Antibody (5D2)
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카탈로그 번호 | CAS 번호 | 설명 | 상태 | 단위 | 판매가 | 할인가 | 가격(VAT포함) | 수량 / 장바구니 / 찜 |
MA518055 | - | Thermo Fisher Scientific MA518055 LPL Monoclonal Antibody (5D2) 100 ul pk | 재고문의 | pk | 831,000원 | - | 914,100원 |
다른 상품 둘러보기
Applications
Tested Dilution
Publications
Western Blot (WB)
Assay-dependent
Immunocytochemistry (ICC/IF)
Assay-dependent
Flow Cytometry (Flow)
1 µg/1x10^6 cells
ELISA (ELISA)
Assay-dependent
Inhibition Assays (IA)
Assay-dependent
Product Specifications
Species Reactivity
Bovine, Chicken, Guinea pig, Human, Rat
Host/Isotype
Mouse / IgG1
Class
Monoclonal
Type
Antibody
Clone
5D2
Immunogen
Purified bovine milk lipoprotein lipase protein if (typeof window.$mangular === undefined
|| !window.$mangular) { window.$mangular = {}; } $mangular.antigenJson = \[{
targetFamily:
LPL,
uniProtId:
P11151-1,
ncbiNodeId:
9913,
antigenRange:
1-478,
antigenLength:
478,
antigenImageFileName:
MA5-18055_LPL_P11151-1_House_mouse.svg,
antigenImageFileNamePDP:
MA5-18055_LPL_P11151-1_House_mouse_PDP.jpeg,
sortOrder:
2}\]
; $mangular.isB2BCMGT = false
; $mangular.isEpitopesModalImageMultiSizeEnabled = true
;
View immunogen .st0{fill:#FFFFFF;} .st1{fill:#1E8AE7;}
Conjugate
Unconjugated Unconjugated Unconjugated
View additional formats
Form
Liquid
Concentration
1 mg/mL
Purification
Protein G
Storage buffer
PBS
Contains
0.09% sodium azide
Storage conditions
Store at 4°C short term. For long term storage, store at -20°C, avoiding freeze/thaw cycles.
Shipping conditions
Ambient (domestic); Wet ice (international)
RRID
AB_2539438
Product Specific Information
This antibody does not recognize hepatic lipase and does not react with mouse samples.
This target has a predicted molecular weight of 53 kDa.
Target Information
LPL encodes lipoprotein lipase, which is expressed in heart, muscle, and adipose tissue. LPL functions as a homodimer, and has the dual functions of triglyceride hydrolase and ligand/bridging factor for receptor-mediated lipoprotein uptake. Severe mutations that cause LPL deficiency result in type I hyperlipoproteinemia, while less extreme mutations in LPL are linked to many disorders of lipoprotein metabolism.
For Research Use Only. Not for use in diagnostic procedures. Not for resale without express authorization.
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