产品名称
Complement C3 Recombinant Rabbit Monoclonal Antibody [JF10-30] - BSA and Azide free
抗体类型
Recombinant Rabbit monoclonal Antibody
免疫原
Synthetic peptide within Human C3 aa 1,210-1,248 / 1,663.
靶点分子量
Predicted band size: 187 kDa
阳性对照
Human liver tissue lysate, HepG2 cell lysate, HeLa cell lysate, Mouse liver tissue lysate, Mouse spleen tissue lysate, Rat liver tissue lysate, Rat spleen tissue lysate, HepG2.
存放说明
Store at 2-8℃. Avoid freeze.
纯化方式
Protein A affinity purified.
功能
C3 plays a central role in the activation of the complement system. Its processing by C3 convertase is the central reaction in both classical and alternative complement pathways. After activation C3b can bind covalently, via its reactive thioester, to cell surface carbohydrates or immune aggregates. Derived from proteolytic degradation of complement C3, C3a anaphylatoxin is a mediator of local inflammatory process. In chronic inflammation, acts as a chemoattractant for neutrophils. It induces the contraction of smooth muscle, increases vascular permeability and causes histamine release from mast cells and basophilic leukocytes. A rare defect of the complement classical pathway. Patients develop recurrent, severe, pyogenic infections because of ineffective opsonization of pathogens. Some patients may also develop autoimmune disorders, such as arthralgia and vasculitic rashes, lupus-like syndrome and membranoproliferative glomerulonephritis.
背景文献
1. Hao W et al. Gut dysbiosis induces the development of depression-like behavior through abnormal synapse pruning in microglia-mediated by complement C3. Microbiome. 2024 Feb
2. Xu L et al. Inhibition of complement C3 signaling ameliorates locomotor and visual dysfunction in autoimmune inflammatory diseases. Mol Ther. 2023 Sep
组织特异性
Plasma. The acylation stimulating protein (ASP) is expressed in adipocytes and released into the plasma during both the fasting and postprandial periods.
翻译后修饰
C3b is rapidly split in two positions by factor I and a cofactor to form iC3b (inactivated C3b) and C3f which is released. Then iC3b is slowly cleaved (possibly by factor I) to form C3c (beta chain + alpha' chain fragment 1 + alpha' chain fragment 2), C3dg and C3f. Other proteases produce other fragments such as C3d or C3g. C3a is further processed by carboxypeptidases to release the C-terminal arginine residue generating the acylation stimulating protein (ASP). Levels of ASP are increased in adipocytes in the postprandial period and by insulin and dietary chylomicrons.; (Microbial infection) C3 is cleaved by Staphylococcus aureus aureolysin; this cleavage renders C3a and C3b inactive. C3b is rapidly degraded by host factors CFH and CFI preventing its deposition on the bacterial surface while C3a is further inactivated by aureolysin.; Phosphorylated by FAM20C in the extracellular medium.
别名
Acylation stimulating protein cleavage product antibody
AHUS5 antibody
ARMD9 antibody
ASP antibody
C3 and PZP like alpha 2 macroglobulin domain containing protein 1 antibody
C3 and PZP-like alpha-2-macroglobulin domain-containing protein 1 antibody
C3 antibody
CO3_HUMAN antibody
Complement C3 antibody
Complement C3c alpha' chain fragment 2 antibody
展开
Acylation stimulating protein cleavage product antibody
AHUS5 antibody
ARMD9 antibody
ASP antibody
C3 and PZP like alpha 2 macroglobulin domain containing protein 1 antibody
C3 and PZP-like alpha-2-macroglobulin domain-containing protein 1 antibody
C3 antibody
CO3_HUMAN antibody
Complement C3 antibody
Complement C3c alpha' chain fragment 2 antibody
Complement component 3 antibody
Complement factor 3 antibody
CPAMD1 antibody
HEL S 62p antibody
折叠
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This data was developed using ET1702-99, the same antibody clone in a different buffer formulation.
Western blot analysis of Complement C3 on different lysates with Rabbit anti-Complement C3 antibody (ET1702-99) at 1/1,000 dilution.
Lane 1: Human liver tissue lysate
Lane 2: HepG2 cell lysate
Lane 3: HeLa cell lysate
Lane 4: Mouse liver tissue lysate
Lane 5: Mouse spleen tissue lysate
Lane 6: Rat liver tissue lysate
Lane 7: Rat spleen tissue lysate
Lysates/proteins at 30 µg/Lane.
Predicted band size: 187 kDa
Observed band size: 108/37 kDa
Exposure time: 1 minute;
4-20% SDS-PAGE gel.
Proteins were transferred to a PVDF membrane and blocked with 5% NFDM/TBST for 1 hour at room temperature. The primary antibody (ET1702-99) at 1/1,000 dilution was used in 5% NFDM/TBST at 4℃ overnight. Goat Anti-Rabbit IgG - HRP Secondary Antibody (HA1001) at 1/50,000 dilution was used for 1 hour at room temperature.
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This data was developed using ET1702-99, the same antibody clone in a different buffer formulation.
Immunocytochemistry analysis of HepG2 cells labeling Complement C3 with Rabbit anti-Complement C3 antibody (ET1702-99) at 1/100 dilution.
Cells were fixed in 100% precooled methanol for 5 minutes at room temperature, then blocked with 1% BSA in 10% negative goat serum for 1 hour at room temperature. Cells were then incubated with Rabbit anti-Complement C3 antibody (ET1702-99) at 1/100 dilution in 1% BSA in PBST overnight at 4 ℃. Goat Anti-Rabbit IgG H&L (iFluor™ 488, HA1121) was used as the secondary antibody at 1/1,000 dilution. PBS instead of the primary antibody was used as the secondary antibody only control. Nuclear DNA was labelled in blue with DAPI.
Beta tubulin (M1305-2, red) was stained at 1/100 dilution overnight at +4℃. Goat Anti-Mouse IgG H&L (iFluor™ 594, HA1126) was used as the secondary antibody at 1/1,000 dilution.
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This data was developed using ET1702-99, the same antibody clone in a different buffer formulation.
Flow cytometric analysis of HepG2 cells labeling Complement C3.
Cells were fixed and permeabilized. Then stained with the primary antibody (ET1702-99, 1μg/mL) (red) compared with Rabbit IgG Isotype Control (green). After incubation of the primary antibody at +4℃ for an hour, the cells were stained with a iFluor™ 488 conjugate-Goat anti-Rabbit IgG Secondary antibody (HA1121) at 1/1,000 dilution for 30 minutes at +4℃. Unlabelled sample was used as a control (cells without incubation with primary antibody; black).
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