Telefon:
+49 (0)241 95 163 153
Fax:
+49 (0)241 95 163 155
E-Mail:
orders@antikoerper-online.de

SARS-Coronavirus Nonstructural Protein 8 Antikörper

(SARS-Coronavirus Nonstructural Protein 8 (SARS-CoV NSP8))
Replicase polyprotein 1ab: Multifunctional protein involved in the transcription and replication of viral RNAs. Contains the proteinases responsible for the cleavages of the polyprotein. Host translation inhibitor nsp1: Inhibits host translation by interacting with the 40S ribosomal subunit. The nsp1-40S ribosome complex further induces an endonucleolytic cleavage near the 5'UTR of host mRNAs, targeting them for degradation. Viral mRNAs are not susceptible to nsp1-mediated endonucleolytic RNA cleavage thanks to the presence of a 5'-end leader sequence and are therefore protected from degradation. By suppressing host gene expression, nsp1 facilitates efficient viral gene expression in infected cells and evasion from host immune response. {ECO:0000269|PubMed:23035226}. Non-structural protein 2: May play a role in the modulation of host cell survival signaling pathway by interacting with host PHB and PHB2. Indeed, these two proteins play a role in maintaining the functional integrity of the mitochondria and protecting cells from various stresses. {ECO:0000269|PubMed:19640993}. Papain-like proteinase: Responsible for the cleavages located at the N-terminus of the replicase polyprotein. In addition, PL-PRO possesses a deubiquitinating/deISGylating activity and processes both 'Lys-48'- and 'Lys-63'-linked polyubiquitin chains from cellular substrates. Participates together with nsp4 in the assembly of virally-induced cytoplasmic double-membrane vesicles necessary for viral replication. Antagonizes innate immune induction of type I interferon by blocking the phosphorylation, dimerization and subsequent nuclear translocation of host IRF3. Prevents also host NF-kappa-B signaling. {ECO:0000269|PubMed:17692280, ECO:0000269|PubMed:19369340}. Non-structural protein 4: Participates in the assembly of virally-induced cytoplasmic double-membrane vesicles necessary for viral replication. {ECO:0000269|PubMed:23943763}. Proteinase 3CL-PRO: Ccleaves the C-terminus of replicase polyprotein at 11 sites. Recognizes substrates containing the core sequence [ILMVF]-Q-|-[SGACN]. Also able to bind an ADP-ribose-1''- phosphate (ADRP). {ECO:0000255|PROSITE-ProRule:PRU00772, ECO:0000269|PubMed:16271890}. Non-structural protein 6: Plays a role in the initial induction of autophagosomes from host reticulum endoplasmic. Later, limits the expansion of these phagosomes that are no longer able to deliver viral components to lysosomes. {ECO:0000269|PubMed:24991833}. Non-structural protein 7: Forms a hexadecamer with nsp8 (8 subunits of each) that may participate in viral replication by acting as a primase. Alternatively, may synthesize substantially longer products than oligonucleotide primers. {ECO:0000269|PubMed:22039154}. Non-structural protein 8: Forms a hexadecamer with nsp7 (8 subunits of each) that may participate in viral replication by acting as a primase. Alternatively, may synthesize substantially longer products than oligonucleotide primers. {ECO:0000269|PubMed:22039154}. Non-structural protein 9: May participate in viral replication by acting as a ssRNA-binding protein. {ECO:0000269|PubMed:19153232}. Non-structural protein 10: Plays a pivotal role in viral transcription by stimulating both nsp14 3'-5' exoribonuclease and nsp16 2'-O-methyltransferase activities. Therefore plays an essential role in viral mRNAs cap methylation. {ECO:0000269|PubMed:22635272}. RNA-directed RNA polymerase: Responsible for replication and transcription of the viral RNA genome. {ECO:0000269|PubMed:22791111}. Helicase: Multi-functional protein with a zinc-binding domain in N-terminus displaying RNA and DNA duplex-unwinding activities with 5' to 3' polarity. Activity of helicase is dependent on magnesium. {ECO:0000269|PubMed:12917423, ECO:0000269|PubMed:22615777}. Guanine-N7 methyltransferase: Enzyme possessing two ssRNA and dsRNA in a 3' to 5' direction and a N7-guanine methyltransferase activity. {ECO:0000269|PubMed:16549795, ECO:0000269|PubMed:20421945, ECO:0000269|PubMed:22635272}. Uridylate-specific endoribonuclease: Mn(2+)-dependent, uridylate-specific enzyme, which leaves 2'-3'-cyclic phosphates 5' to the cleaved bond. 2'-O-methyltransferase: Methyltransferase that mediates mRNA cap 2'-O-ribose methylation to the 5'-cap structure of viral mRNAs. N7-methyl guanosine cap is a prerequisite for binding of nsp16. Therefore plays an essential role in viral mRNAs cap methylation which is essential to evade immune system. {ECO:0000269|PubMed:18417574, ECO:0000269|PubMed:20421945, ECO:0000305}.
SARS-Coronavirus Nonstructural Protein 8 (SARS-CoV NSP8) Antikörper SARS-Coronavirus Nonstructural Protein 8 (SARS-CoV NSP8) Antikörper SARS-Coronavirus Nonstructural Protein 8 (SARS-CoV NSP8) Antikörper (ABIN7270151)

SARS-CoV NSP8 Reaktivität: SARS Coronavirus-2 (SARS-CoV-2) IF, WB Wirt: Kaninchen Polyclonal unconjugated

SARS-Coronavirus Nonstructural Protein 8 (SARS-CoV NSP8) Antikörper SARS-Coronavirus Nonstructural Protein 8 (SARS-CoV NSP8) Antikörper SARS-Coronavirus Nonstructural Protein 8 (SARS-CoV NSP8) Antikörper (ABIN7270150)

SARS-CoV NSP8 Reaktivität: SARS Coronavirus-2 (SARS-CoV-2) IF, WB Wirt: Kaninchen Monoclonal unconjugated

SARS-Coronavirus Nonstructural Protein 8 Antikörper nach Reaktivität

Hier sind SARS-Coronavirus Nonstructural Protein 8 Antikörper für eine Vielzahl von Species wie anti-SARS Coronavirus-2 (SARS-CoV-2) SARS-Coronavirus Nonstructural Protein 8 zu finden. Die unten aufgeführten Species gehören zu den verfügbaren Arten. Klicken Sie auf einen Link, um zu den entsprechenden Produkten zu gelangen.

SARS-Coronavirus Nonstructural Protein 8 Antikörper nach Anwendung

Hier sind SARS-Coronavirus Nonstructural Protein 8 Antikörper zu finden, welche für eine bestimmte Anwendung wie IF, WB validiert wurde. Einige der verfügbaren Anwendungen sind unten aufgeführt. Klicken Sie auf einen Link, um zu den entsprechenden Produkten zu gelangen.

SARS-Coronavirus Nonstructural Protein 8 Antikörper nach Wirt

Hier sind SARS-Coronavirus Nonstructural Protein 8 Antikörper mit einem spezifischen Wirt zu finden. Die hier aufgeführten Wirt sind einige der verfügbaren. Ein Klick auf den entsprechenden Link führt zu den Produkten.

SARS-Coronavirus Nonstructural Protein 8 Antikörper nach Klonalität

Finden Sie verfügbare monoklonale oder polyklonale SARS-Coronavirus Nonstructural Protein 8 Antikörper. Klicken Sie auf einen Link, um zu den entsprechenden Produkten zu gelangen.

Häufig verwendete SARS-Coronavirus Nonstructural Protein 8 Antikörper

Produkt
Reaktivität
Applikation
Validierungen
Kat. Nr.
Menge
Datenblatt
Reaktivität SARS Coronavirus-2 (SARS-CoV-2)
Applikation IF, WB
Validierungen
  • (2)
Kat. Nr. ABIN7270151
Menge 100 μL
Datenblatt Datenblatt
Reaktivität SARS Coronavirus-2 (SARS-CoV-2)
Applikation IF, WB
Validierungen
  • (2)
Kat. Nr. ABIN7270150
Menge 100 μL
Datenblatt Datenblatt

Aktuelle Publikationen für unsere SARS-Coronavirus Nonstructural Protein 8 Antikörper

Ng, Faulkner, Finsterbusch, Wu, Harvey, Hussain, Greco, Liu, Kjaer, Swanton, Gandhi, Beale, Gamblin, Cherepanov, McCauley, Daniels, Howell, Arase, Wack, Bauer, Kassiotis: "SARS-CoV-2 S2-targeted vaccination elicits broadly neutralizing antibodies." in: Science translational medicine, Vol. 14, Issue 655, pp. eabn3715, (2022) (PubMed).

Tan, Rijal, Rahikainen, Keeble, Schimanski, Hussain, Harvey, Hayes, Edwards, McLean, Martini, Pedrera, Thakur, Conceicao, Dietrich, Shelton, Ludi, Wilsden, Browning, Zagrajek, Bialy, Bhat et al.: "A COVID-19 vaccine candidate using SpyCatcher multimerization of the SARS-CoV-2 spike protein receptor-binding domain induces potent neutralising antibody responses. ..." in: Nature communications, Vol. 12, Issue 1, pp. 542, (2021) (PubMed).

Johnson, Drugan, Miller, Evans: "38" in: , Vol. 1363, Issue Nucleic acids research, pp. 28-39, (1991)

Snijder, van der Meer, Zevenhoven-Dobbe, Onderwater, van der Meulen, Koerten, Mommaas: "Ultrastructure and origin of membrane vesicles associated with the severe acute respiratory syndrome coronavirus replication complex." in: Journal of virology, Vol. 80, Issue 12, pp. 5927-40, (2006) (PubMed).

Zuo, Mattern, Tan, Li, Hall, Sterner, Shoo, Tran, Lim, Sarafianos, Kazi, Navas-Martin, Weiss, Butt: "Expression and purification of SARS coronavirus proteins using SUMO-fusions." in: Protein expression and purification, Vol. 42, Issue 1, pp. 100-10, (2005) (PubMed).

Putics, Filipowicz, Hall, Gorbalenya, Ziebuhr: "ADP-ribose-1"-monophosphatase: a conserved coronavirus enzyme that is dispensable for viral replication in tissue culture." in: Journal of virology, Vol. 79, Issue 20, pp. 12721-31, (2005) (PubMed).

Zuo, Li, Hall, Mattern, Tran, Shoo, Tan, Weiss, Butt: "Enhanced expression and purification of membrane proteins by SUMO fusion in Escherichia coli." in: Journal of structural and functional genomics, Vol. 6, Issue 2-3, pp. 103-11, (2005) (PubMed).

Ivanov, Thiel, Dobbe, van der Meer, Snijder, Ziebuhr: "Multiple enzymatic activities associated with severe acute respiratory syndrome coronavirus helicase." in: Journal of virology, Vol. 78, Issue 11, pp. 5619-32, (2004) (PubMed).

Malakhov, Mattern, Malakhova, Drinker, Weeks, Butt: "SUMO fusions and SUMO-specific protease for efficient expression and purification of proteins." in: Journal of structural and functional genomics, Vol. 5, Issue 1-2, pp. 75-86, (2004) (PubMed).

Prentice, McAuliffe, Lu, Subbarao, Denison: "Identification and characterization of severe acute respiratory syndrome coronavirus replicase proteins." in: Journal of virology, Vol. 78, Issue 18, pp. 9977-86, (2004) (PubMed).

Aliase für SARS-Coronavirus Nonstructural Protein 8 Antikörper

orf1ab polyprotein (pp1ab) (orf1ab) Antikörper
pp1a Antikörper
pp1ab Antikörper
Sie sind hier:
Kundenservice