ZAP-70/Syk (pTyr319) Antikörper

Details zu Produkt Nr. ABIN968885, Anbieter: Anmelden zum Anzeigen
Antigen
Epitop
pTyr319
9
4
3
3
Reaktivität
Human, Maus, Ratte (Rattus)
12
7
4
Wirt
Maus
7
5
Klonalität (Klon)
Monoklonal ()
Konjugat
Unkonjugiert
3
1
1
1
1
1
Applikation
Flow Cytometry (FACS), Western Blotting (WB)
7
4
3
Optionen
Hersteller
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Hersteller Produkt- Nr.
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Immunogen Human phosphorylated ZAP70 Peptide
Klon 17A-P
Isotyp IgG1
Kreuzreaktivität Maus, Ratte (Rattus)
Produktmerkmale 1. Since applications vary, each investigator should titrate the reagent to obtain optimal results.
2. Please refer to us for technical protocols.
3. Caution: Sodium azide yields highly toxic hydrazoic acid under acidic conditions. Dilute azide compounds in running water before discarding to avoid accumulation of potentially explosive deposits in plumbing.
4. Source of all serum proteins is from USDA inspected abattoirs located in the United States.
Reinigung The monoclonal antibody was purified from tissue culture supernatant or ascites by affinity chromatography.
Hintergrund ZAP70 is a protein tyrosine kinase (PTK) that associates with the z subunit of the T cell antigen receptor (TCR) and undergoes tyrosine phosphorylation following TCR stimulation. ZAP70 contains two SH2-like domains with the PTK domain located at the C-terminus. It appears that both ZAP70 and Syk are recruited to the phosphorylated CD3 and z subunits after TCR stimulation. TCR stimulation leads to autophosphorylation of ZAP70 at Tyr-315 amd Tyr-319, and mutation of the Tyr-319 site dramatically impairs TCR signaling. In addition, TCR-mediated Lck activity leads to phosphorylation of ZAP70 on Tyr-493 in the regulatory loop of the kinase domain leading to upregulation of ZAP70 kinase activity. The significance of ZAP70 activation in mediating TCR signal transduction has been confirmed by showing that ZAP70 activity is absent in an autosomal recessive form of severe combined immunodeficiency (SCID). This is due to mutations affecting the ZAP70 kinase domain which affect the stability of the protein and TCR signaling. Clone 17A/P-ZAP70 recognizes the phosphorylated form of ZAP70 (Y319). It also cross-reacts with SYK (Y352) due to homology of the phosphorylation site with ZAP70 (Y319). The PE-conjugated format has been evaluated using human and mouse model systems. The unconjugated form of the antibody (ABIN968884) has also been shown to work in western blot analysis on human, mouse, and rat cells.
Molekulargewicht 70 kDa
Applikationshinweise For flow cytometry we recommend to use conjugated versions of ZAP70 (pY319)/Syk (pY352) antibody: (Alexa Fluor® 647 ZAP70 (pY319)/Syk (pY352)), 557818 (Alexa Fluor® 488 ZAP70 (pY319)/Syk (pY352)), 557881 (PE ZAP70 (pY319)/Syk (pY352)). For purified version AP70 (pY319)/Syk (pY352) as a second step for flow cytometry, we recommend to use of clone A85-1 in either FITC or PE.
Beschränkungen Nur für Forschungszwecke einsetzbar
Format Liquid
Konzentration 250 μg/mL
Buffer Aqueous buffered solution containing BSA, glycerol, and ≤0.09 % sodium azide.
Konservierungsmittel Sodium azide
Vorsichtsmaßnahmen This product contains Sodium azide: a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.
Lagerung -20 °C
Informationen zur Lagerung Store undiluted at -20° C.
Bilder des Herstellers
 image for anti-ZAP-70/Syk (pTyr319) antibody (ABIN968885) Jurkat cells were treated with 1 mM pervanadate for 15 minutes at 37°C, then either l...
Produkt verwendet in: Di Bartolo, Mège, Germain, Pelosi, Dufour, Michel, Magistrelli, Isacchi, Acuto: "Tyrosine 319, a newly identified phosphorylation site of ZAP-70, plays a critical role in T cell antigen receptor signaling." in: The Journal of biological chemistry, Vol. 274, Issue 10, pp. 6285-94, 1999 (PubMed).

Arpaia, Shahar, Dadi, Cohen, Roifman: "Defective T cell receptor signaling and CD8+ thymic selection in humans lacking zap-70 kinase." in: Cell, Vol. 76, Issue 5, pp. 947-58, 1994 (PubMed).

Chan, Kadlecek, Elder, Filipovich, Kuo, Iwashima, Parslow, Weiss: "ZAP-70 deficiency in an autosomal recessive form of severe combined immunodeficiency." in: Science (New York, N.Y.), Vol. 264, Issue 5165, pp. 1599-601, 1994 (PubMed).

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