Thermo Fisher Scientific LPL Polyclonal Antibody
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카탈로그 번호 | CAS 번호 | 설명 | 상태 | 단위 | 판매가 | 할인가 | 가격(VAT포함) | 수량 / 장바구니 / 찜 |
PA534812 | - | Thermo Fisher Scientific PA534812 LPL Polyclonal Antibody 100 ul pk | 재고문의 | pk | 700,000원 | - | 770,000원 |
다른 상품 둘러보기
Applications
Tested Dilution
Publications
Western Blot (WB)
1:500-1:3,000
Immunohistochemistry (Paraffin) (IHC (P))
Assay-dependent
Product Specifications
Species Reactivity
Mouse
Host/Isotype
Rabbit / IgG
Class
Polyclonal
Type
Antibody
Immunogen
Recombinant protein fragment contains a sequence corresponding to a region within amino acids 134 and 354 (P06858) of LPL if (typeof window.$mangular === undefined
|| !window.$mangular) { window.$mangular = {}; } $mangular.antigenJson = \[{
targetFamily:
LPL,
uniProtId:
P06858-1,
ncbiNodeId:
9606,
antigenRange:
134-354,
antigenLength:
475,
antigenImageFileName:
PA5-34812_LPL_P06858-1_Rabbit.svg,
antigenImageFileNamePDP:
PA5-34812_LPL_P06858-1_Rabbit_PDP.jpeg,
sortOrder:
1}\]
; $mangular.isB2BCMGT = false
; $mangular.isEpitopesModalImageMultiSizeEnabled = true
;
View immunogen .st0{fill:#FFFFFF;} .st1{fill:#1E8AE7;}
Conjugate
Unconjugated Unconjugated Unconjugated
Form
Liquid
Concentration
1.35 mg/mL
Purification
Antigen affinity chromatography
Storage buffer
PBS, pH 7, with 20% glycerol
Contains
0.025% ProClin 300
Storage conditions
Store at 4°C short term. For long term storage, store at -20°C, avoiding freeze/thaw cycles.
Shipping conditions
Wet ice
RRID
AB_2552164
Product Specific Information
Recommended positive controls: A431, H1299, HeLa, Molt-4.
Predicted reactivity: Human (99%), Mouse (96%), Rat (95%), Cat (97%), Pig (96%), Rabbit (96%), Chicken (80%), Sheep (96%), Bovine (96%), Guinea pig (90%).
Store product as a concentrated solution. Centrifuge briefly prior to opening the vial.
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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