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AB124769

Anti-Factor H antibody [EPR6226]

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(1 Publication)

Rabbit Recombinant Monoclonal Factor H antibody. Suitable for WB and reacts with Human samples. Cited in 1 publication.

View Alternative Names

HF, HF1, HF2, CFH, Complement factor H, H factor 1

1 Images
Western blot - Anti-Factor H antibody [EPR6226] (AB124769)
  • WB

Unknown

Western blot - Anti-Factor H antibody [EPR6226] (AB124769)

All lanes:

Western blot - Anti-Factor H antibody [EPR6226] (ab124769) at 1/1000 dilution

Lane 1:

A549 cell lysate at 10 µg

Lane 2:

Human fetal lung lysate at 10 µg

Lane 3:

Human fetal liver lysate at 10 µg

Lane 4:

Human kidney lysate at 10 µg

Lane 5:

Human plasma lysate at 10 µg

Secondary

All lanes:

Goat anti-Rabbit HRP at 1/2000 dilution

Predicted band size: 139 kDa

false

Key facts

Host species

Rabbit

Clonality

Monoclonal

Clone number

EPR6226

Isotype

IgG

Carrier free

No

Reacts with

Human

Applications

WB

applications

Immunogen

The exact immunogen used to generate this antibody is proprietary information.

Reactivity data

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Product details

Species reactivity
Mouse, Rat: We have preliminary internal testing data to indicate this antibody may not react with these species.
Please contact us for more information.

Patented technology
Our RabMAb® technology is a patented hybridoma-based technology for making rabbit monoclonal antibodies. For details on our patents, please refer to RabMAb® patents.

What are the advantages of a recombinant monoclonal antibody?
This product is a recombinant monoclonal antibody, which offers several advantages including:

  • - High batch-to-batch consistency and reproducibility
  • - Improved sensitivity and specificity
  • - Long-term security of supply
  • - Animal-free batch production

For more information, read more on recombinant antibodies.

Properties and storage information

Form
Liquid
Purification technique
Affinity purification Protein A
Storage buffer
pH: 7.2 - 7.4 Preservative: 0.05% Sodium azide Constituents: 50% Tissue culture supernatant, 40% Glycerol (glycerin, glycerine), 9.85% Tris glycine
Shipped at conditions
Blue Ice
Appropriate short-term storage conditions
+4°C
Appropriate long-term storage conditions
-20°C
Storage information
Stable for 12 months at -20°C

Supplementary information

This supplementary information is collated from multiple sources and compiled automatically.

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.
Biological function summary

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.

Pathways

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.

Product protocols

For this product, it's our understanding that no specific protocols are required. You can visit:

Target data

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.
See full target information CFH

Publications (1)

Recent publications for all applications. Explore the full list and refine your search

Communications biology 8:976 PubMed40595293

2025

Macrophages foster anti-tumor immunity by ZEB1-dependent cytotoxic T cell chemoattraction.

Applications

Unspecified application

Species

Unspecified reactive species

Kathrin Fuchs,Elisabetta D'Avanzo,Isabell Armstark,Ruthger van Roey,Ana Clavel Ezquerra,Nino Bindel,Katharina Siebenkäs,Yussuf Hajjaj,Renato Liguori,Fulvia Ferrazzi,Lukas Amon,Johanna Bulang,Julian Hübner,Marcel Edler,Ece Grace,Annemarie Schwab,Marwin Alfredo,Maria Faas,Jochen Ackermann,Elena Percivalle,Claudia Günther,Markus H Hoffmann,Gerhard Krönke,Christoph Becker,Diana Dudziak,Philipp Arnold,Miriam Woehner,Falk Nimmerjahn,Simone Brabletz,Marc P Stemmler,Thomas Brabletz,Harald Schuhwerk
View all publications

Product promise

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For full details, please see our Terms & Conditions

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