lyo NZYSupreme qPCR Probe Master Mix
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lyo NZYSupreme qPCR Probe Master Mix

Description: Lyo NZYSupreme qPCR Probe Master Mix (2x) is an optimized and highly efficient freeze-dried reaction mixture developed for realtime PCR. This master mix was engineered with a dual hot-start enzyme control mechanism to provide the highest detection sensitivity. In addition, the latest developments in PCR enhancers have been incorporated in the Lyo NZYSupreme qPCR Probe Master Mix, including buffer chemistry and incorporation of highly robust engineered enzymes. This master mix does not contain ROX and it was specifically developed for probe-detection technology, including molecular beacons. For qPCR instruments that require ROX reference dye, please add ROX (Cat. No. MB406) according to the table presented in the section “ROX reference dye”. Lyo NZYSupreme qPCR Probe Master Mix (2x) is provided as a simple-to-use, stabilized 2x reaction mixture that includes all components for quantitative PCR, except sample DNA, primers, probe and water.

Features:
– Eco-friendly room temperature shipment
– Stable at room temperature for 1 month
– Dual hot-start mode
– Ultra-sensitive: detects low-copy number targets
– Batch-to-batch reproducibility
– Intra-batch reproducibility
– Simple and reproducible
– Compatible with multiple real-time platforms

Components:
– Lyo NZYSupreme qPCR Probe Master Mix (2x)
– qPCR master mix reconstitution buffer

Applications:
– Real-time qPCR
– Two-step RT-qPCR
– Developed for probe-detection technology

New Lyo qPCR Probe Master Mix (2x)

Lyo NZYSupreme qPCR Probe Master Mix (2x)

Description: Lyo NZYSupreme qPCR Probe Master Mix (2x) is an optimized and highly efficient freeze-dried reaction mixture developed for realtime PCR. This master mix was engineered with a dual hot-start enzyme control mechanism to provide the highest detection sensitivity. In addition, the latest developments in PCR enhancers have been incorporated in the Lyo NZYSupreme qPCR Probe Master Mix, including buffer chemistry and incorporation of highly robust engineered enzymes. This master mix does not contain ROX and it was specifically developed for probe-detection technology, including molecular beacons. For qPCR instruments that require ROX reference dye, please add ROX (Cat. No. MB406) according to the table presented in the section “ROX reference dye”. Lyo NZYSupreme qPCR Probe Master Mix (2x) is provided as a simple-to-use, stabilized 2x reaction mixture that includes all components for quantitative PCR, except sample DNA, primers, probe and water.

lyo NZYSupreme qPCR Probe Master Mix
lyo NZYSupreme qPCR Probe Master Mix

Features:
– Eco-friendly room temperature shipment
– Stable at room temperature for 1 month
– Dual hot-start mode
– Ultra-sensitive: detects low-copy number targets
– Batch-to-batch reproducibility
– Intra-batch reproducibility
– Simple and reproducible
– Compatible with multiple real-time platforms

Components:
– Lyo NZYSupreme qPCR Probe Master Mix (2x)
– qPCR master mix reconstitution buffer

AceQ qPCR Probe Master Mix

Q112-03 2500 rxn (20 μl/rxn)
EUR 646

HotTaq Probe qPCR Mix (ROX)

BT11001 250rxn
EUR 109
Description: High quality HotTaq polymerase for different PCR variations and downstream applications.

HotTaq Probe qPCR Mix (Capillary)

BT11003 250rxn
EUR 109
Description: High quality HotTaq polymerase for different PCR variations and downstream applications.

HotTaq Probe qPCR Universal Mix

BT11004 250rxn
EUR 123
Description: High quality HotTaq polymerase for different PCR variations and downstream applications.

AceQ U+ Probe Master Mix

Q113-02 500 rxn (20 μl/rxn)
EUR 267

AceQ U+ Probe Master Mix

Q113-03 2500 rxn (20 μl/rxn)
EUR 842

SYBR Green qPCR Master Mix

HY-K0501 5 mL (500 rxns)
EUR 263

RT Master Mix for qPCR

HY-K0510 1 mL (100 rxns)
EUR 291

HotTaq Probe qPCR Mix (no ROX)

BT11002 250rxn
EUR 109
Description: High quality HotTaq polymerase for different PCR variations and downstream applications.

Fast Probe Master Mix (200 rxn)

31005 2x1ML
EUR 234
Description: Minimum order quantity: 1 unit of 2x1ML

Fast Probe Master Mix (500 rxn)

31005-1 5x1ML
EUR 466
Description: Minimum order quantity: 1 unit of 5x1ML

Fast Probe Master Mix (5000 rxn)

31005-2 50x1ML
EUR 3871
Description: Minimum order quantity: 1 unit of 50x1ML

ChamQ Geno-SNP Probe Master Mix

Q811-02 500 rxn (20 μl/rxn)
EUR 277

ChamQ Geno-SNP Probe Master Mix

Q811-03 2500 rxn (20 μl/rxn)
EUR 923

2x SYBR Green qPCR Master Mix

B21202 5 mL
EUR 224
Description: Our 2x SYBR Green qPCR master mix performs toe to toe in all qPCR assays with the most well known brands on the market but surpases them significantly in cost-efficiency.

2x SYBR Green qPCR Master Mix

B21203 25 mL
EUR 856
Description: Our 2x SYBR Green qPCR master mix performs toe to toe in all qPCR assays with the most well known brands on the market but surpases them significantly in cost-efficiency.

AceQ Universal SYBR qPCR Master Mix

Q511-02 500 rxn (20 μl/rxn)
EUR 221

AceQ Universal SYBR qPCR Master Mix

Q511-03 2500 rxn (20 μl/rxn)
EUR 646

ChamQ Universal SYBR qPCR Master Mix

Q711-02 500 rxn (20 μl/rxn)
EUR 221

ChamQ Universal SYBR qPCR Master Mix

Q711-03 2500 rxn (20 μl/rxn)
EUR 646

Accuris qMax Probe No Rox qPCR Mix

PR2001-N-1000 1 PC
EUR 467.74
  • To order instruments in 115V / US plug please delete the 'E' off the order code.European 2 pin plugs will be supplied as standard, please request UK if required.

AceQ U+ Universal Probe Master Mix V2

Q513-02 500 rxn (20 μl/rxn)
EUR 267

AceQ U+ Universal Probe Master Mix V2

Q513-03 2500 rxn (20 μl/rxn)
EUR 842

SYBR Green qPCR Master Mix (High ROX)

HY-K0521 1 mL (100 rxns)
EUR 113

SYBR Green qPCR Master Mix (Low ROX)

HY-K0522 5 mL (500 rxns )
EUR 257

SYBR Green qPCR Master Mix (No ROX)

HY-K0523 5 mL (500 rxns )
EUR 257

miRNA Universal SYBR® qPCR Master Mix

MQ101-01 125 rxn(20 μl/rxn)
EUR 138

miRNA Universal SYBR® qPCR Master Mix

MQ101-02 500 rxn(20 μl/rxn)
EUR 242

 

 

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Sars cov 2 binding antibodies

The immune response to severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) infection is initiated by innate immune activation followed by antigen-specific T and B cell responses. An important mechanism that protects against viral diseases is the presence of virus-neutralizing antibodies, which is similar for almost all viruses that cause acute illness followed by the elimination of pathogens.

Accordingly, all currently available antiviral vaccines are primarily intended to induce virus-neutralizing antibodies. Neutralizing antibodies generally block the binding of the virus to cell receptors.

In some cases, neutralizing antibodies can prevent the conformational changes necessary for virus fusion with the cell membrane or proteolytic cleavage. Neutralizing antibodies against SARS-CoV-2 are directed against the peak protein (S), which contains multiple antigenic epitopes in the receptor-binding domain (RBD) and non-RBD epitopes.

An important neutralization mechanism is to block the binding of RBD to angiotensin-converting enzyme 2 (ACE2), the virus’s cellular receptor. RBD is located at the tip of protein S. The receptor-binding motif (RBM) consists of approximately 70 aa within RBD and represents the actual amino acids that directly interact with ACE2.

Coronaviruses get their names from the typical spikes that are formed by the spike protein (S) that inserts into the lipid bilayer membrane of the virus. The receptor-binding domain (RBD) and its receptor-binding motif (RBM) allow interaction with the cell-surface receptor ACE2 that mediates entry of the virus into host cells.

This can be blocked by neutralizing antibodies. Therefore, most of the neutralizing epitopes are found on RBD / RBM. In addition to protein S, SARS-CoV-2 has two other viral surface proteins (not shown): envelope (E) and matrix (M).

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Elastase from Porcine Pancreas

Related Categories: Application rate, Biochemicals and reagents, Enzymes, Inhibitors and substrates, Isolation of proteins and nucleic acids

Quality level: 100

Form: lyophilized

Specific activity: ≥25 units / mg protein

Storage condition:

OK to freeze
Dried

Storage conditions: -20C

General description

Elastase is native to the porcine pancreas. Serine protease that catalyzes the hydrolysis of proteins and peptides (especially at bonds adjacent to neutral amino acid residues), including albumin, casein, denatured collagen, elastin, fibrin, and hemoglobin, and of various synthetic substrates containing aspartic acid, phenylalanine, or tyrosine. Inhibited by DFP, elastin, and α2-macroglobulin.

Elastase is native to the porcine pancreas. Catalyzes the hydrolysis of proteins and peptides (especially at bonds adjacent to neutral amino acid residues), including albumin, casein, denatured collagen, elastin, fibrin, and hemoglobin, and of various synthetic substrates containing aspartic acid, glutamic acid, phenylalanine, or tyrosine. Preferably it cleaves peptide bonds at the carbonyl end of amino acid residues with small hydrophobic side chains, such as glycine, valine, leucine, isoleucine, and particularly alanine. Inhibited by DFP, elastin, and α2-macroglobulin. It has an optimal pH of 7.8-8.5; pI = 9.5.

Packaging

1000, 250 u in plastic ampoule

Warning

Toxicity: Standard handling (A)

Definition of unit

One unit is defined as the amount of enzyme that will hydrolyze 1.0 mole of Suc-Ala-Ala-Pro-Abu-PNA (catalog # 324699) per minute at 25 ° C, pH 8.0.

Physical form

Lyophilized from 50 mM trehalose, 1 mM acetic acid.

Reconstitution

After reconstitution, elastase can be stored at 4 ° C at pH 6.0 for long-term use. If incubated at room temperature at or near its optimum pH, elastase rapidly autolyzes to a mixture of peptides. Stock solutions are stable for up to 2 months at 4 ° C, pH 6.0.

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ELHGHII – Human/Monkey IgG anti-human

General description

The product binds human IgG and not other human Ig. Immunoglobulins are composed of antigen-binding domains of two fragments (Fab) and one crystallizable fragment (Fc). The gene encoding the IgG gene cluster is found on human chromosome 14. Anti-human IgG antiserum (Fc specific) is produced in goat using purified human IgG, Fc fragment, as an immunogen. Affinity isolated antibody is obtained from goat anti-human IgG antiserum by immunospecific purification that removes essentially all goat serum proteins, including immunoglobulins, that do not specifically bind to the Fc fragment of human IgG.

Specificity

Specificity for the human IgG Fc fragment is determined by ELISA and immunoelectrophoresis (IEP). The antibody preparation is specific for human IgG, Fc fragment when tested against purified human IgA, IgG (Fc and Fab fragments), IgM, Bence Jones kappa, and Bence Jones lambda myeloma proteins. No reactivity is observed with the Fab fragment of human IgG, light chains, IgA or IgM. The affinity-purified anti-human IgG (Fc-specific) reagent offers the advantage of increased sensitivity for human IgG without cross-reactivity with other substances present on the cell membrane or surface.

The lack of cross-species cross-reactivity with mouse or rat serum proteins makes this product excellent for screening human monoclonal antibodies produced by hybridoma cells grown in vivo in mouse or rat ascites fluids. This product has the ability to detect all subclasses of human IgG in human biological fluids or tissues from normal or pathological situations such as cancer or autoimmune diseases. It is effective as a second antibody reagent in immunoassay procedures and can be used as a starting material for conjugates using enzymes or fluorescent dyes.

Immunogen

Anti-human IgG antiserum (Fc specific) is produced in goats using purified human IgG, Fc fragment, as an immunogen

Request

The anti-human IgG antibody (specific for Fc) produced in goats has been used:

  • in double capture ELISA to measure antiglobulin responses in the serum of transplant patients treated with monoclonal antibodies CD52 (CAMPATH-1G)
  • in the detection of IgG levels in patients with rheumatoid arthritis
  • in small bowel biopsies
  • in patients with acute myocardial infarction by immunoblotting

Physical form

The solution in 0.01 M phosphate-buffered saline, pH 7.4, containing 15 mM sodium azide

Storage and stability

For continuous use, store at 2-8 ° C for up to one month. For long-term storage, the solution can be frozen in working aliquots. Repeated freezing and thawing, or storing in “frost-free” freezers is not recommended. If slight cloudiness occurs after prolonged storage, rinse the solution by centrifugation before use.

Disclaimer

Unless otherwise stated in our catalog or other company documentation accompanying the product (s), our products are designed for research use only and are not to be used for any other purpose, including but not limited to commercial uses. unauthorized, in vitro diagnostic uses, ex vivo or in vivo therapeutic uses or any type of consumption or application to humans or animals.

Biochemical / Physiological Actions

The IgG antibody subtype is the most abundant of the serum immunoglobulins of the immune system. It is secreted by B cells and is found in blood and extracellular fluids and provides protection against infections caused by bacteria, fungi, and viruses. Maternal IgG is transferred to the fetus through the placenta, which is vital for the newborn’s immune defense against infection. Mutations in the Fc region of IgG are implicated in autoimmune diseases such as rheumatoid arthritis. Modified Fc proteins are of therapeutic importance for the treatment of autoimmune diseases.

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Glypican-3 (GPC3), 1G12

Immunogen: Recombinant fragment containing amino acids 511-580 of human Glypican 3 (1G12); Full-length recombinant human GPC3 protein (GPC3 / 863)

Location: Cytoplasmic

Marker: Hepatocellular carcinoma marker

Specificity

Glypican-3 (GPC3) is an integral membrane protein that is mutated in Simpson-Golabi-Behmel syndrome (GBSS). SGBS is characterized by pre-and postnatal overgrowth and is an X-linked recessive condition. GPC3 can also be found in secreted form. Anti-GPC3 has been identified as a useful tumor marker for the diagnosis of hepatocellular carcinoma (HCC), hepatoblastoma, melanoma, testicular germ cell tumors, and Wilms tumor.

In HCC patients, GPC3 is overexpressed in neoplastic liver tissue and elevated in serum, but is undetectable in normal liver, benign liver, and serum from healthy donors. GPC3 expression is also found to be higher in HCC liver tissue than in cirrhotic liver or liver with focal lesions such as dysplastic nodules and areas of liver adenoma (HA) with malignant transformation. In the context of testicular germ cell tumors, GPC3 expression is up-regulated in certain histological subtypes, specifically yolk sac tumors and choriocarcinoma.

 

A high level of GPC3 expression has also been found in some types of embryonal tumors, such as Wilm’s tumor and hepatoblastoma, with low or undetectable expression in adjacent normal tissue. In thyroid cancer patients, GPC3 expression is dramatically improved in certain types of cancers: 100% in follicular carcinoma and 70% in papillary carcinoma. The expression of GPC3 in follicular carcinoma was significantly higher than that of follicular adenoma. In contrast, GPC 3 is not expressed in anaplastic carcinoma.

Isotype: IgG

Clonality: Monoclonal

Host: Mouse

Gene: GPC3

Purity: Purified Protein A or G

Innovator’s reward: Try on a species/app not listed above to receive a full credit towards a future purchase.

Applications / Dilutions

Dilutions

  • Flow cytometry 0.5 – 1 ug / million cells in 0.1 ml
  • Immunocytochemistry / Immunofluorescence 1-2 ug / ml
  • Immunohistochemistry
  • Immunohistochemistry-Paraffin 0.5 – 1.0 ug / ml
  • Immunofluorescence 0.5 – 1.0 ug / ml

Application notes

  • Immunohistochemistry (formalin-fixed): 1-2 ug/ml for 30 minutes at RT. Staining of formalin-fixed tissues requires heating tissue sections in 1 mM EDTA buffer, pH 7.5-8.5, for 45 min at 95 ° C followed by cooling at RT for 20 min.
  • The optimal dilution for a specific application must be determined.

Theoretical MW

  • 67 kDa.
  • Disclaimer Note: The observed molecular weight of the protein may vary from the listed predicted molecular weight due to post-translational modifications, post-translation cleavages, relative charges, and other experimental factors.

Packaging, storage, and formulations

Storage: Store at 4C.

Buffer: 10 mM PBS with 0.05% BSA

Preservative: 0.05% sodium azide

Concentration: 0.2mg / ml

Purity: Purified Protein A or G

Alternative names for the Glypican 3 antibody (1G12 + GPC3 / 863)

  • DGSX
  • Glypican 3
  • glypican 3 proteoglycan
  • glypican-3
  • GPC3
  • GTR2-2
  • proteoglycan heparan sulfate
  • OCI-5 intestinal protein
  • MXR7
  • OCI5
  • OCI-5
  • glypican-3 secreted
  • SGB
  • SGBS
  • SGBS1SDYS

Limitations

This product is for research use only and is not approved for human use or clinical diagnosis. Primary Antibodies are guaranteed for 1 year from the date of receipt.

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Anti-Human Glycan-3 25 µg

Resume

Anti-glycan antibodies are an abundant subpopulation of serum antibodies with critical functions in many immune processes. Changes in the levels of these antibodies can occur with the onset of disease, exposure to pathogens, or vaccination. As a result, there has been significant interest in exploiting anti-glycan antibodies as biomarkers for many diseases. The serum contains a mixture of anti-glycan antibodies that can recognize the same antigen, and competition for binding can potentially influence the detection of antibody subpopulations that are more relevant to disease processes.

The most abundant antibody isotypes in serum are IgG, IgM, and IgA, but little is known about how these different isotypes compete for the same glucan antigen. In this study, we developed a multiplexed glucan microarray assay and applied it to assess how different isotypes of anti-glucan antibodies (IgA, IgG, and IgM) compete for the imprinted glycan antigens. While IgG and IgA antibodies generally outperform IgM for peptide or protein antigens, we found that IgM outperformed IgG and IgA on many glucan antigens.

To illustrate the importance of this effect, we provide evidence that IgM competition may explain the unexpected observation that IgG of certain antigenic specificities appears to be preferentially transported from mothers to fetuses. We show that IgM in maternal serum competes with IgG resulting in lower than expected IgG signals. Since cord blood contains very low levels of IgM, competition only affects maternal IgG signals, making it appear that certain IgG antibodies are higher in cord blood than matched maternal blood. Taken together, the results highlight the importance of competition for studies involving anti-glycan antibodies.

Introduction

Human serum contains a wide variety of carbohydrate-binding antibodies that play a critical role in human health and provide a rich pool of potential biomarkers for many biomedical applications and diseases. For example, the detection of anti-glycan antibodies against blood group A and B antigens provides a simple and reliable strategy to predict which individuals are suitable for transfusion and transplantation. Anti-glycan antibodies are also crucial in other areas of immunology, such as tumor surveillance, autoimmunity, defense against pathogens, and response to vaccines.

These broader immune functions have stimulated interest in exploring the potential use of circulating anti-glycan antibodies as biomarkers for a wide variety of diseases. Detection of antiglycan antibodies in serum is typically carried out by immobilizing a carbohydrate of interest, capturing specific antibodies, and then measuring the amounts of bound antibodies.

This process is complicated by the fact that serum often contains a mixture of antibodies that recognize the same antigen, and certain antibodies within the mixture may be more relevant to immune protection or disease processes than others. Antibodies against a particular glycan can vary in terms of affinity, specificity, concentration, and/or isotype, but they can all compete to bind to the same antigen. As a result, the binding of one can influence the detection of the others, and it can be difficult to reliably measure a subpopulation of target antibodies of interest.

Results

Our approach to assessing competence involved the use of purified IgG, IgA, and IgM antibodies from pooled human serum. Each polyclonal antibody sample would be profiled on our glycan microarray individually and in the presence of other isotypes. In addition, changes in IgG and IgM anti-glycan antibody signals would be assessed in whole serum after the addition of IgG, IgA, and IgM. Although IgD and IgE are also present in serum at low concentrations and capable of competing, this study focused on the most abundant antibodies in serum.

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cd 34 Progenitor cells 250 nm 2 ml

Related categories: Cell culture, Cells, Hematopoietic stem cell culture, Human blood, and stem cell culture, Primary cell culture

Biological source: human umbilical cord blood

Packaging: 100,000 cells pack

Morphology: (parent)

Application (s): cell culture | mammal: suitable

Shipped: on dry ice

Storage temperature: −196 ° C

Request

CD34 is a glycosylated transmembrane protein and represents a well-known marker for primitive progenitor cells derived from blood and bone marrow, especially for hematopoietic and endothelial stem cells. Although the biological functions of CD34 are largely unknown, recent data suggest that CD34 is involved in maintaining progenitor cells in a phenotypically undifferentiated state.

PromoCell offers CD34 + progenitor cells from healthy donor umbilical cord blood. CD34 + progenitor cells contain two main cell subpopulations, hematopoietic and endothelial progenitor cells. Thus, CD34 + progenitor cells are suitable for a number of studies, e.g. Eg directed differentiation into more compromised blood cell types and endothelial lineages.

Quality

Rigid quality control tests are performed for each lot of CD34 + progenitor cells. They are routinely characterized by flow cytometry that analyzes viability, cell size, and the presence of significant markers, ie, CD34. Additionally, all cells have been tested for the absence of HIV-1, HIV-2, HBV, HCV, HTLV-1, HTLV-2, and microbial contaminants (fungi, bacteria, and mycoplasmas).

Warning

Although tests for HIV-1, HIV-2, HBV, HCV, HTLV-1, and HTLV-2 were negative, cells, like all products of human origin, should be handled as potentially infectious. No test procedure can completely guarantee the absence of infectious agents.

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Anti-ACE2 Antibody

The protein encoded by this gene belongs to the angiotensin-converting enzyme family of dipeptidyl carboxypeptidases and has considerable homology to the human angiotensin 1 converting enzyme. This secreted protein catalyzes the cleavage of angiotensin I into angiotensin 1-9, and angiotensin II into the vasodilator angiotensin 1-7.

The organ- and cell-specific expression of this gene suggests that it may play a role in the regulation of cardiovascular and renal function, as well as fertility. In addition, the encoded protein is a functional receptor for the spike glycoprotein of the human coronavirus HCoV-NL63 and the human severe acute respiratory syndrome coronaviruses, SARS-CoV and SARS-CoV-2 (COVID-19 virus)

Cat # +Size A2072-100
Size 100 μg
Antibody Target ACE2
Alternate Name Angiotensin-converting enzyme 2; ACE-related carboxypeptidase; Angiotensin-converting enzyme homolog; ACEH; Metalloprotease MPROT15
Host Rabbit
Antibody Type Polyclonal
Isotype IgG
Immunogen Recombinant Human Angiotensin-converting enzyme 2 protein (395-638 aa)
Accession # Q9BYF1
Gene ID 59272
Appearance Colorless liquid
Formulation In 0.01 M PBS, pH 7.4, 50% Glycerol, 0.03% proclin 300
Purification Affinity purified
Species Reactivity Human
Application Immunofluorescence (IF), Immunohistochemistry (IHC)
Application & Usage IHC 1:20-1:200, IF 1:50-1:200
Handling The antibody solution should be gently mixed before use.
Storage Conditions -20ºC
Shipping Conditions Gel Pack
USAGE For Research Use Only! Not For Use in Humans.
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Antibodies

Coronaviruses are large, enveloped, positive-sense RNA viruses that are known to affect humans, birds, and mammals. These viruses have a genome length of 30 kb. The 5′-terminal of the viral genome encodes a polyprotein that upon cleavage yields several non-structural proteins that play important roles in viral transcription and replication. The 3′-terminal encodes 4 structural proteins, namely, Spike (S), Envelope (E), Membrane (M), and Nucleocapsid (N) that have an essential role in the synthesis of viral RNA and viral replication.

There are 6 known Coronaviruses that infect humans. Of these, two are known to cause severe diseases with high rates of mortality: Severe Acute Respiratory Syndrome Coronavirus (SARS-CoV) and Middle-East Respiratory Syndrome Coronavirus (MERS-CoV). Recently, a group of Chinese scientists discovered another strain of Coronavirus that caused a massive viral outbreak in China.

This virus is more deadly than SARS-CoV and MERS-CoV combined and is named SARS-CoV-2 (previously COVID-19). Since very little information available regarding the role of the COVID-19 proteins in viral pathogenesis and replication, not many treatment options are available. In addition to this, there are limited antibodies available in the market to detect these proteins.

BioVision is pleased to announce the launch of Coronavirus Antibodies, the first in the market. These antibodies specialize in detecting the Coronavirus disease 2019 nucleoprotein (SARS-CoV-2, COVID-19), SARS, and MERS. They have been tested using research techniques such as Western Blot, ELISA, Immunofluorescence, and Immunohistochemistry. These antibodies are available in both polyclonal and monoclonal formats and can readily be shipped worldwide.

Can these antibodies detect COVID-19/SARS-CoV-2?
Yes, some of our Coronavirus antibodies can detect COVID-19/SARS-CoV-2.