Thermo Fisher Scientific Angiotensinogen Monoclonal Antibody (8)
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카탈로그 번호 | CAS 번호 | 설명 | 상태 | 단위 | 판매가 | 할인가 | 가격(VAT포함) | 수량 / 장바구니 / 찜 |
MA529008 | - | Thermo Fisher Scientific MA529008 Angiotensinogen Monoclonal Antibody (8) 100 ul pk | 재고문의 | pk | 0원 | - | 0원 |
다른 상품 둘러보기
Applications
Tested Dilution
Publications
Immunocytochemistry (ICC/IF)
1:20-1:100
Flow Cytometry (Flow)
1:25-1:100
Product Specifications
Host/Isotype
Mouse / IgG2a
Class
Monoclonal
Type
Antibody
Clone
08
Immunogen
Recombinant Human SerpinA8/Angiotensinogen/AGT protein (Met1-Ala485) if (typeof window.$mangular === undefined
|| !window.$mangular) { window.$mangular = {}; } $mangular.antigenJson = \[{
targetFamily:
Angiotensinogen,
uniProtId:
P01019-1,
ncbiNodeId:
9606,
antigenRange:
1-485,
antigenLength:
485,
antigenImageFileName:
MA5-29008_Angiotensinogen_P01019-1_House_mouse.svg,
antigenImageFileNamePDP:
MA5-29008_Angiotensinogen_P01019-1_House_mouse_PDP.jpeg,
sortOrder:
1}\]
; $mangular.isB2BCMGT = false
; $mangular.isEpitopesModalImageMultiSizeEnabled = true
;
View immunogen .st0{fill:#FFFFFF;} .st1{fill:#1E8AE7;}
Conjugate
Unconjugated Unconjugated Unconjugated
Form
Liquid
Concentration
1 mg/mL
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_2784946
Product Specific Information
This product is preservative free. It is recommended to add sodium azide to avoid contamination (final concentration 0.05%-0.1%).
This antibody has specificity for Human SerpinA8/Angiotensinogen/AGT.
Target Information
The protein encoded by AGT, pre-angiotensinogen or angiotensinogen precursor, is expressed in the liver and is cleaved by the enzyme renin in response to lowered blood pressure. The resulting product, angiotensin I, is then cleaved by angiotensin converting enzyme (ACE) to generate the physiologically active enzyme angiotensin II. The protein is involved in maintaining blood pressure and in the pathogenesis of essential hypertension and preeclampsia. Mutations in this gene are associated with susceptibility to essential hypertension, and can cause renal tubular dysgenesis, a severe disorder of renal tubular development. Defects in this gene have also been associated with non-familial structural atrial fibrillation, and inflammatory bowel disease.
For Research Use Only. Not for use in diagnostic procedures. Not for resale without express authorization.
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