Mouse Monoclonal Factor H antibody. Suitable for ELISA, WB and reacts with Recombinant full length protein - Human, Human, Purified native protein samples. Cited in 8 publications.
Preservative: 0.02% Sodium azide
Constituents: PBS
ELISA | WB | |
---|---|---|
Human | Expected | Tested |
Purified native protein | Not recommended | Tested |
Recombinant full length protein - Human | Tested | Not recommended |
Species | Dilution info | Notes |
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Species Recombinant full length protein - Human | Dilution info 10 µg/mL | Notes - |
Species | Dilution info | Notes |
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Species Human | Dilution info Use at an assay dependent concentration. | Notes - |
Species | Dilution info | Notes |
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Species Purified native protein | Dilution info - | Notes - |
Species | Dilution info | Notes |
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Species Human, Purified native protein | Dilution info - | Notes - |
Species | Dilution info | Notes |
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Species Recombinant full length protein - Human | Dilution info - | Notes - |
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Glycoprotein that plays an essential role in maintaining a well-balanced immune response by modulating complement activation. Acts as a soluble inhibitor of complement, where its binding to self markers such as glycan structures prevents complement activation and amplification on cell surfaces (PubMed:21285368, PubMed:25402769). Accelerates the decay of the complement alternative pathway (AP) C3 convertase C3bBb, thus preventing local formation of more C3b, the central player of the complement amplification loop (PubMed:19503104, PubMed:26700768). As a cofactor of the serine protease factor I, CFH also regulates proteolytic degradation of already-deposited C3b (PubMed:18252712, PubMed:23332154, PubMed:28671664). In addition, mediates several cellular responses through interaction with specific receptors. For example, interacts with CR3/ITGAM receptor and thereby mediates the adhesion of human neutrophils to different pathogens. In turn, these pathogens are phagocytosed and destroyed (PubMed:20008295, PubMed:9558116). (Microbial infection) In the mosquito midgut, binds to the surface of parasite P.falciparum gametocytes and protects the parasite from alternative complement pathway-mediated elimination.
HF, HF1, HF2, CFH, Complement factor H, H factor 1
Mouse Monoclonal Factor H antibody. Suitable for ELISA, WB and reacts with Recombinant full length protein - Human, Human, Purified native protein samples. Cited in 8 publications.
Preservative: 0.02% Sodium azide
Constituents: PBS
Purified from TCS.
ab118820 has switched from ascites to TCS on 19th September 2019. Lot numbers higher than GR3258447 are from tissue culture supernatant.
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Factor H also known as complement factor H is an important regulatory protein in the complement system. It has a molecular mass of approximately 155 kDa. This protein is mainly expressed in the liver but it can also be found in low levels in other tissues. Factor H serves as a control element for complement activation particularly affecting the alternative pathway. It binds to C3b a central component of the complement system and accelerates the decay of C3 convertase as well as promotes the proteolytic inactivation of C3b by factor I.
Factor H limits the activity of the complement system to prevent damage to host tissues. The protein exists in the plasma in a soluble form. It functions by recognizing host cell surfaces via specific markers avoiding inappropriate activation. Factor H belongs to a group of proteins which include other regulators of complement activation. These proteins maintain the balance between effective immune defense and protection of host tissue from excessive immune responses.
Factor H is a part of the alternative complement pathway. This pathway is important for innate immune response involving proteins like factor P (properdin) which stabilizes C3 convertase. Factor H modulates these interactions to prevent unwarranted complement activity on host cells. Another related pathway is the classic complement pathway although factor H's involvement here is less direct since it primarily regulates the alternative pathway.
Factor H associations include atypical hemolytic uremic syndrome and age-related macular degeneration. Factor H deficiency or dysfunction can lead to uncontrolled complement activation resulting in kidney damage in atypical hemolytic uremic syndrome where it is also related to factor I. Additionally in age-related macular degeneration variants in the factor H gene are linked to increased susceptibility further highlighting the protein's importance in regulating immune responses.
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This species and application combination has not been tested, but we predict it will work based on strong homology. However, this combination is not covered by our product promise.
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Terms & Conditions.
This blot was produced using a 4-12% Bis-tris under the MOPS buffer system. The gel was run at 200V for 55 minutes before being transferred onto a Nitrocellulose membrane at 30V for 70 minutes. The membrane was then blocked for an hour using 3% milk before being incubated with ab118820 overnight at 4°C at a 1ug/ml concentration. Antibody binding was detected using Goat anti-Mouse IgG H&L (IRDye® 800CW) preadsorbed (Goat anti-Mouse IgG H&L (IRDye® 800CW) preadsorbed ab216772) at 1/20000 dilution for 1 hour at room temperature before imaging.
This image was generated using the ascites version of the product.
All lanes: Western blot - Anti-Factor H antibody [OX-24] (ab118820) at 1 µg/mL
Lane 1: Human serum diluted 1/100 at 10 µL
Lane 2: Human plasma diluted 1/100 at 10 µL
Lane 3: Purified Factor H protein at 0.5 µg
Lane 4: Purified Factor H protein at 0.1 µg
Performed under reducing conditions.
Predicted band size: 139 kDa
Observed band size: 170 kDa
96-well microtitre plates were coated overnight at 4°C with recombinant human C3, C3b, iC3b, and Factor H proteins, in duplicate at a concentration of 1μg/mL. Plates were blocked with 1% BSA in PBS-T (0.1% Tween®) for 1 hour before incubation with a 10-step 4x serial dilution of ab118820 from 10μg/mL for 1 hour at room temperature. Antibody binding was detected with Goat Anti-Mouse IgG H&L (HRP) (Goat Anti-Mouse IgG H&L (HRP) ab6789) secondary antibody at a 1 in 10000 dilution for 1 hour at room temperature. Plates were incubated with TMB ELISA substrate for 7 minutes prior to being stopped with Stop solution and absorbance measured at 450nm.
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