Thermo Fisher Scientific Complement C5a Monoclonal Antibody (2942)
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카탈로그 번호 | CAS 번호 | 설명 | 상태 | 단위 | 판매가 | 할인가 | 가격(VAT포함) | 수량 / 장바구니 / 찜 |
MA140161 | - | Thermo Fisher Scientific MA140161 Complement C5a Monoclonal Antibody (2942) 100 ug pk | 재고문의 | pk | 817,000원 | - | 898,700원 |
다른 상품 둘러보기
Applications
Tested Dilution
Publications
Western Blot (WB)
1:50
Immunohistochemistry (Frozen) (IHC (F))
1:50
ELISA (ELISA)
1:50
Functional Assay (Functional)
Assay-dependent
Product Specifications
Species Reactivity
Human
Host/Isotype
Mouse / IgG2a
Class
Monoclonal
Type
Antibody
Clone
2942
Immunogen
Neo-epitope on C5a.
Conjugate
Unconjugated Unconjugated Unconjugated
Form
Liquid
Concentration
0.1 mg/mL
Purification
Protein G
Storage buffer
PBS with 0.1% BSA
Contains
no preservative
Storage conditions
4° C
Shipping conditions
Ambient (domestic); Wet ice (international)
RRID
AB_1073837
Product Specific Information
MA1-40161 detects C5a/C5a des-Arg from human samples.
MA1-40161 has been successfully used in Western blot, ELISA, immunohistochemistry (frozen), and functional assay applications. By Western blot, the antibody detects a band size of 14 kDa.
The MA1-40161 immunogen is the Neo-epitope on C5a.
Positive control: Eye tissue of patient with AMD; Negative control: Eye tissue of patient without AMD.
Endotoxin <24 EU/mg.
General comment: Please notice that under given conditions it is known that C5 can expose epitopes normally only found in the cleaved activation products.
Target Information
The protein encoded by this gene is the fifth component of complement, which plays an important role in inflammatory and cell killing processes. This protein is comprised of alpha and beta polypeptide chains that are linked by a disulfide bridge. An activation peptide, C5a, which is an anaphylatoxin that possesses potent spasmogenic and chemotactic activity, is derived from the alpha polypeptide via cleavage with a convertase. The C5b macromolecular cleavage product can form a complex with the C6 complement component, and this complex is the basis for formation of the membrane attack complex, which includes additional complement components. Mutations in this gene cause complement component 5 deficiency, a disease where patients show a propensity for severe recurrent infections. Defects in this gene have also been linked to a susceptibility to liver fibrosis and to rheumatoid arthritis.
For Research Use Only. Not for use in diagnostic procedures. Not for resale without express authorization.
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