Dieser Anti-SARS-CoV-2 Spike Antikörper ist ein Kaninchen Polyklonal Antikörper zur Detektion von SARS-CoV-2 Spike in ELISA, WB, IF und IHC. Geeignet für SARS Coronavirus-2 (SARS-CoV-2) und SARS Coronavirus (SARS-CoV). Dieses Primary Antibody wurde in 11+ Publikationen zitiert.
Dieser SARS-CoV-2 Spike Antikörper ist unkonjugiert
Applikation
ELISA, Western Blotting (WB), Immunofluorescence (IF), Immunohistochemistry (IHC)
Bindungsspezifität
C-Term
Homologie
Predicted reactivity based on immunogen sequence: SARS-CoV Spike proteins: (100%)
Aufreinigung
Affinity chromatography purified via peptide column
Immunogen
Anti-SARS-CoV-2 (COVID-19, 2019-nCoV) Spike antibody was raised against a peptide corresponding to 20 amino acids near the carboxy terminus of SARS-CoV-2 (COVID-19, 2019-nCoV) Spike glycoprotein. The immunogen is located within the last 50 amino acids of SARS-CoV-2 (COVID-19, 2019-nCoV) Spike protein.
SARS-CoV-2 S
Reaktivität: SARS Coronavirus-2 (SARS-CoV-2)
ELISA, Neut, GICA
Wirt: Human
Monoclonal
A1
Fc Tag
single-domain Antibody (sdAb)
Recombinant Antibody
Research Grade
SARS-CoV-2 S
Reaktivität: SARS Coronavirus-2 (SARS-CoV-2)
ELISA, FACS
Wirt: Human
Monoclonal
CR3022
unconjugated
Recombinant Antibody
Applikationshinweise
WB: 1 μg/mL; IF: 1 μg/mL. IHC: 0.2 μg/mL
Beschränkungen
Nur für Forschungszwecke einsetzbar
Format
Liquid
Konzentration
1 mg/mL
Buffer
The antibody is supplied in PBS containing 0.02% sodium azide.
Konservierungsmittel
Sodium azide
Vorsichtsmaßnahmen
This product contains sodium azide: a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.
Handhabung
As with all antibodies care should be taken to avoid repeated freeze thaw cycles. Antibodies should not be exposed to prolonged high temperatures.
Lagerung
4 °C/-20 °C
Informationen zur Lagerung
Antibody can be stored at 4˚C for three months and -20˚C, stable for up to one year.
Haltbarkeit
12 months
Wardhana, Kuntaman, Utomo, Aryananda, Rifdah, Wafa, Shahnaz, Ningrum, Cininta, Ariani, Van Lith, Dachlan: "Evidence of Placental Villous Inflammation and Apoptosis in Third-Trimester Symptomatic SARS-CoV-2 Maternal Infection." in: Yonsei medical journal, Vol. 65, Issue 4, pp. 202-209, (2024) (PubMed).
Basu, Penumutchu, Nguyen, Mbonye, Tolbert, Karn, Komar, Mazumder: "A Structurally Conserved RNA Element within SARS-CoV-2 ORF1a RNA and S mRNA Regulates Translation in Response to Viral S Protein-Induced Signaling in Human Lung Cells." in: Journal of virology, Vol. 96, Issue 2, pp. e0167821, (2022) (PubMed).
El Jamal, Pujadas, Ramos, Bryce, Grimes, Amanat, Tsankova, Mussa, Olson, Salem, Miorin, Aydillo, Schotsaert, Albrecht, Liu, Marjanovic, Francoeur, Sebra, Sealfon, García-Sastre, Fowkes, Cordon-Cardo et al.: "Tissue-Based SARS-Cov-2 Detection in Fatal COVID-19 Infections: Sustained Direct Viral-Induced Damage is Not Necessary to Drive Disease Progression. ..." in: Human pathology, (2021) (PubMed).
Garifullina, Shen: "High-throughput fabrication of high aspect ratio Ag/Al nanopillars for optical detection of biomarkers." in: Journal of materials chemistry. B, (2021) (PubMed).
Magro, Mulvey, Berlin, Nuovo, Salvatore, Harp, Baxter-Stoltzfus, Laurence: "Complement associated microvascular injury and thrombosis in the pathogenesis of severe COVID-19 infection: A report of five cases." in: Translational research : the journal of laboratory and clinical medicine, Vol. 220, pp. 1-13, (2020) (PubMed).
Mulvey, Magro, Ma, Nuovo, Baergen: "Analysis of complement deposition and viral RNA in placentas of COVID-19 patients." in: Annals of diagnostic pathology, Vol. 46, pp. 151530, (2020) (PubMed).
Nuovo, Tili, Suster, Matys, Hupp, Magro et al.: "Strong homology between SARS-CoV-2 envelope protein and a Mycobacterium sp. antigen allows rapid diagnosis of Mycobacterial infections and may provide specific anti-SARS-CoV-2 immunity via the BCG ..." in: Annals of diagnostic pathology, Vol. 48, pp. 151600, (2020) (PubMed).
Nuovo, Magro, Mikhail: "Cytologic and molecular correlates of SARS-CoV-2 infection of the nasopharynx." in: Annals of diagnostic pathology, Vol. 48, pp. 151565, (2020) (PubMed).
Nuovo, Magro, Shaffer, Awad, Suster, Mikhail, He, Michaille, Liechty, Tili: "Endothelial cell damage is the central part of COVID-19 and a mouse model induced by injection of the S1 subunit of the spike protein." in: Annals of diagnostic pathology, Vol. 51, pp. 151682, (2020) (PubMed).
Ventura, Cennamo, Minopoli, Campanile, Censi, Terracciano, Portella, Velotta: "Colorimetric Test for Fast Detection of SARS-CoV-2 in Nasal and Throat Swabs." in: ACS sensors, Vol. 5, Issue 10, pp. 3043-3048, (2020) (PubMed).
Funari, Chu, Shen: "Detection of antibodies against SARS-CoV-2 spike protein by gold nanospikes in an opto-microfluidic chip." in: Biosensors & bioelectronics, Vol. 169, pp. 112578, (2020) (PubMed).
Target
SARS-CoV-2 Spike (SARS-CoV-2 S)
Andere Bezeichnung
SARS-CoV-2 Spike
Substanzklasse
Viral Protein
Hintergrund
Coronavirus disease 2019 (COVID-19), formerly known as 2019-nCoV acute respiratory disease, is an infectious disease caused by SARS-CoV-2, a virus closely related to the SARS virus. The disease is the cause of the 2019–20 coronavirus outbreak. The structure of 2019-nCoV consists of the following: a Spike protein (S), hemagglutinin-esterease dimer (HE), a membrane glycoprotein (M), an envelope protein (E) a nucleoclapid protein (N) and RNA. Coronavirus invades cells through Spike (S) glycoproteins, a class I fusion protein. It is the major viral surface protein that coronavirus uses to bind to the human cell surface receptor. It also mediates the fusion of host and viral cell membrane, allowing the virus to enter human cells and begin infection. The spike protein is the major target for neutralizing antibodies and vaccine development. The protein modeling suggests that there is strong interaction between Spike protein receptor-binding domain and its host receptor angiotensin-converting enzyme 2 (ACE2), which regulate both the cross-species and human-to-human transmissions of COVID-19. The recent study has shown that the SARS-CoV-2 spike protein binds ACE2 with higher affinity than SARS-CoV spike protein .