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C1S (riliprubart Biosimilar) Recombinant Monoclonal Antibody

C1S (riliprubart Biosimilar) Recombinant Monoclonal Antibody

Code: CSB-RA003657MB1HU

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Size:

100ug

100ug500ug1mg5mg10mg50mg100mg200mg

US$199

Quantity:

Species Reactivity: Human

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Product Details
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Target Background

Product Details

Uniprot NO.

P09871

Target Names

C1S

Alternative Names

Basic proline rich peptide IB 1 antibody; C1 esterase antibody; C1S antibody; C1S_HUMAN antibody; Complement C1s subcomponent antibody; Complement C1s subcomponent heavy chain antibody; Complement C1s subcomponent light chain antibody; Complement component 1 s subcomponent antibody; Complement component 1 subcomponent s antibody; FLJ44757 antibody

Species Reactivity

Human

Immunogen

Recombinant Human C1S protein

Immunogen Species

Homo sapiens (Human)

Conjugate

Non-conjugated

Clonality

Monoclonal

Concentration

It differs from different batches. Please contact us to confirm it.

Buffer

0.01M PBS，pH7.4

Form

Liquid
Note: We will preferentially ship the format that we have in stock, however, if you have any special requirement for the format, please remark your requirement when placing the order, we will prepare according to your demand.

Storage

Upon receipt, store at -20°C or -80°C. Avoid repeated freeze.

Notes

Validation Status
Application-specific performance (e.g., in flow cytometry, ELISA, IHC or other assay formats) has not yet been experimentally verified by CUSABIO. Users are advised to determine the optimal working conditions empirically in their own assay systems.
Guaranteed Quality
① Antibody purity > 95% tested by SDS-PAGE.
② Endotoxin level < 0.1EU/ug tested by LAL method.

Lead Time

In stock
Note: All of our proteins are default shipped with normal blue ice packs, if you request to ship with dry ice, please communicate with us in advance and extra fees will be charged.

Usage

It is a non-therapeutic biosimilar antibody, owning the same variable region from the corresponding approved therapeutic antibody. In conclusion, it is a research-grade biosimilar antibody and expressed in mammalian cell, which can be directly used as positive controls in drug discovery or used for rapid verification of the biological functions of target protein.

Datasheet & COA

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Description

This recombinant monoclonal antibody is a research-grade biosimilar to riliprubart, designed for research involving C1S (complement component 1s), a serine protease critical to the classical complement pathway. C1S functions as part of the C1 complex, where it cleaves C4 and C2 to initiate the complement cascade, a key component of innate immunity. Dysregulated C1S activity contributes to various complement-mediated disorders, including autoimmune diseases, transplant rejection, and conditions involving excessive inflammation. Aberrant classical pathway activation has been implicated in cold agglutinin disease, antibody-mediated rejection, and certain inflammatory neuropathies.

Riliprubart represents a therapeutic antibody developed to selectively inhibit C1S, thereby modulating classical complement activation while preserving alternative pathway function. As a research-grade biosimilar, this antibody enables investigators to explore C1S biology, validate complement inhibition strategies, and study disease mechanisms where classical pathway dysregulation plays a pathogenic role. It serves as a valuable tool for immunology research, complement pathway studies, and preclinical investigations into complement-targeted therapeutic approaches.

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Target Background

Function(From Uniprot)

C1s B chain is a serine protease that combines with C1q and C1r to form C1, the first component of the classical pathway of the complement system. C1r activates C1s so that it can, in turn, activate C2 and C4.

Gene References into Functions

TNT003, an inhibitor of the serine protease C1s, prevents complement activation induced by cold agglutinins. PMID:24695853
Data indicate that complement C1s mRNA level was low in ICR-derived glomerulonephritis (ICGN) mice liver as compared with age-matched ICR mice. PMID:23989031
A molecular switch governs the interaction between the human complement protease C1s and its substrate, complement C4. PMID:23592783
Four positively charged amino acids on the serine protease domain appear to form a catalytic exosite that is required for efficient cleavage of C4 in the classical pathway of complement. PMID:22855709
Detailed mapping of post-translational modifications and insights into the C1r/C1s binding sites. PMID:20008834
Interaction with the prime side residues at the cleavage point in C1s enhances the affinity of the enzyme for complement 2 and complement 4 substrates; these prime subsite residues mediate positive cooperativity in the cleavage of the substrate. PMID:14674770
full specificity of the enzyme using a randomized phage display library PMID:16169853
There are splice variants of C1s mRNA transcripts in normal human cells PMID:18062908