IRAK1 Polyklonaler Antikörper

• Featured Product
• KD/KO Validated

IRAK1 Polyklonal Antikörper für FC, IF, IHC, IP, WB, ELISA

Wirt / Isotyp

Kaninchen / IgG

Getestete Reaktivität

human, Maus, Ratte

Anwendung

WB, RIP, IP, IHC, IF, FC, ELISA

Konjugation

Unkonjugiert

Publikationen

31

Kat-Nr. : 10478-2-AP

Synonyme

IRAK, IRAK 1, IRAK1, pelle

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Galerie der Validierungsdaten

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  WB analysis of HEK-293 using 10478-2-AP

  WB result of IRAK1 antibody (10478-2-AP; 1:2000; incubated at room temperature for 1.5 hours) with sh-Control and sh-IRAK1 transfected HEK-293 cells.

• 

  WB analysis using 10478-2-AP

  Various lysates were subjected to SDS PAGE followed by western blot with 10478-2-AP (IRAK1 antibody) at dilution of 1:1500 incubated at room temperature for 1.5 hours.

• 

  WB analysis of RAW 264.7 using 10478-2-AP

  RAW 264.7 cells were subjected to SDS PAGE followed by western blot with 10478-2-AP (IRAK1 antibody) at dilution of 1:300 incubated at room temperature for 1.5 hours.

• 

  WB analysis of PC-12 using 10478-2-AP

  PC-12 cells were subjected to SDS PAGE followed by western blot with 10478-2-AP (IRAK1 antibody) at dilution of 1:600 incubated at room temperature for 1.5 hours.

• 

  WB analysis of PC-13 using 10478-2-AP

  PC-13 cells were subjected to SDS PAGE followed by western blot with 10478-2-AP (IRAK1 Antibody) at dilution of 1:600 incubated at room temperature for 1.5 hours.

• 

  WB analysis using 10478-2-AP

  Various lysates were subjected to SDS PAGE followed by western blot with 10478-2-AP (IRAK1 antibody) at dilution of 1:3000 incubated at room temperature for 1.5 hours.

• 

  IP experiment of HeLa using 10478-2-AP

  IP Result of anti-IRAK1 (IP:10478-2-AP, 4ug; Detection:10478-2-AP 1:600) with HeLa cells lysate 2800ug.

• 

  IHC staining of human lung cancer using 10478-2-AP

  Immunohistochemical analysis of paraffin-embedded human lung cancer tissue slide using 10478-2-AP (IRAK1 antibody) at dilution of 1:600 (under 10x lens). Heat mediated antigen retrieval with Tris-EDTA buffer (pH 9.0).

• 

  IHC staining of human lung cancer using 10478-2-AP

  Immunohistochemical analysis of paraffin-embedded human lung cancer tissue slide using 10478-2-AP (IRAK1 antibody) at dilution of 1:600 (under 40x lens). Heat mediated antigen retrieval with Tris-EDTA buffer (pH 9.0).

• 

  IHC staining of human lung cancer using 10478-2-AP

  Immunohistochemical analysis of paraffin-embedded human lung cancer tissue slide using 10478-2-AP (IRAK1 antibody) at dilution of 1:200 (under 10x lens). Heat mediated antigen retrieval with Tris-EDTA buffer (pH 9.0).

• 

  IHC staining of human lung cancer using 10478-2-AP

  Immunohistochemical analysis of paraffin-embedded human lung cancer tissue slide using 10478-2-AP (IRAK1 antibody) at dilution of 1:200 (under 40x lens). Heat mediated antigen retrieval with Tris-EDTA buffer (pH 9.0).

• 

  IHC staining of human lung cancer using 10478-2-AP

  Immunohistochemical analysis of paraffin-embedded human lung cancer tissue slide using 10478-2-AP (IRAK1 Antibody) at dilution of 1:50 (under 10x lens).

• 

  IHC staining of human lung cancer using 10478-2-AP

  Immunohistochemical analysis of paraffin-embedded human lung cancer tissue slide using 10478-2-AP (IRAK1 Antibody) at dilution of 1:50 (under 40x lens).

• 

  IF Staining of HeLa using 10478-2-AP

  Immunofluorescent analysis of (4% PFA) fixed HeLa cells using IRAK1 antibody (10478-2-AP) at dilution of 1:200 and CoraLite®488-Conjugated AffiniPure Goat Anti-Rabbit IgG(H+L), CL555-Phalloidin (orange).

• 

  FC experiment of HeLa using 10478-2-AP

  1X10^6 HeLa cells were intracellularly stained with 0.4 ug Anti-Human IRAK1 (10478-2-AP) and CoraLite®488-Conjugated AffiniPure Goat Anti-Rabbit IgG(H+L) at dilution 1:1000 (red), or 0.4 ug Control Antibody. Cells were fixed with 4% PFA and permeabilized with Flow Cytometry Perm Buffer (PF00011-C).

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Geprüfte Anwendungen

• Erfolgreiche Detektion in WB: A549-Zellen, HEK-293-Zellen, HeLa-Zellen, Jurkat-Zellen, K-562-Zellen, MCF-7-Zellen, PC-12-Zellen, PC-13-Zellen, RAW 264.7-Zellen
• Erfolgreiche IP: HeLa-Zellen
• Erfolgreiche Detektion in IHC: humanes Lungenkarzinomgewebe; Hinweis: Antigendemaskierung mit TE-Puffer pH 9,0 empfohlen. (*) Wahlweise kann die Antigendemaskierung auch mit Citratpuffer pH 6,0 erfolgen.
• Erfolgreiche Detektion in IF: HeLa-Zellen
• Erfolgreiche Detektion in FC: HeLa-Zellen

Empfohlene Verdünnung

• Western Blot (WB): WB : 1:500-1:3000
• Immunpräzipitation (IP): IP : 0.5-4.0 ug for 1.0-3.0 mg of total protein lysate
• Immunhistochemie (IHC): IHC : 1:300-1:1200
• Immunfluoreszenz (IF): IF : 1:50-1:500
• Durchflusszytometrie (FC): FC : 0.40 ug per 10^6 cells in a 100 µl suspension

It is recommended that this reagent should be titrated in each testing system to obtain optimal results.

Sample-dependent, check data in validation data gallery

Veröffentlichte Anwendungen

• KD/KO: See 2 publications below
• WB: See 30 publications below
• IHC: See 6 publications below
• IF: See 2 publications below
• RIP: See 1 publications below

Produktinformation

10478-2-AP bindet in WB, RIP, IP, IHC, IF, FC, ELISA IRAK1 und zeigt Reaktivität mit human, Maus, Ratten

• Getestete Reaktivität: human, Maus, Ratte
• In Publikationen genannte Reaktivität: human, Maus, Ratte
• Wirt / Isotyp: Kaninchen / IgG
• Klonalität: Polyklonal
• Typ: Antikörper
• Immunogen: IRAK1 fusion protein Ag0728
• Vollständiger Name: interleukin-1 receptor-associated kinase 1
• Berechnetes Molekulargewicht: 77 kDa
• Beobachtetes Molekulargewicht: 68-80 kDa
• GenBank-Zugangsnummer: BC014963
• Gene symbol: IRAK1
• Gene ID (NCBI): 3654
• Konjugation: Unkonjugiert
• Form: Liquid
• Reinigungsmethode: Antigen-Affinitätsreinigung
• Lagerungspuffer: PBS mit 0.02% Natriumazid und 50% Glycerin pH 7.3.
• Lagerungsbedingungen: Bei -20°C lagern. Nach dem Versand ein Jahr lang stabil Aliquotieren ist bei -20^oC Lagerung nicht notwendig. 20ul Größen enthalten 0,1% BSA.

Hintergrundinformationen

Interleukin-1 receptor-associated kinases (IRAKs) are a unique family of death domain containing protein kinases that play a key role in initiating innate immune response against foreign pathogens. They are involved in Toll-like receptor (TLR) and interleukin-1 receptor (IL-1R) signaling pathways. IRAK1 is the first member of this kinase family. Upon ligand binding to TLR/IL-1R, IRAK1 is recruited by MYD88 to the receptor-signaling complex, the association leads to IRAK1 phosphorylation by IRAK4 and subsequent autophosphorylation and kinase activation. Hyper-phosphorylated IRAK1 then disengages from the receptor complex, and forms a cytosolic IRAK1-TRAF6 complex. TRAF6 then interacts with TAK and TAB, resulting in eventual activation of the NF-κB and MAPK pathways. Phosphorylated IRAK1 also undergoes ubiquitin-mediated degradation or sumoylation, which results in nuclear translocation and transcriptional activation of inflammatory target genes. (PMID: 17890055; 12620219)

Publikationen

Species	Application	Title
human	WB	Blood; Targeting of microRNA-142-3p in dendritic cells regulates endotoxin-induced mortality.; Authors - Sun Yaping Y
mouse	WB	Cell Rep; METTL3-mediated m6A mRNA methylation regulates neutrophil activation through targeting TLR4 signaling; Authors - Shuhua Luo
mouse	WB,IHC	J Crohns Colitis; A Molecular Targeted Immunotherapeutic Strategy for Ulcerative Colitis via Dual-targeting Nanoparticles Delivering miR-146b to Intestinal Macrophages.; Authors - Feihong Deng
mouse	WB	Cell Mol Immunol; The deubiquitinase OTUB1 augments NF-κB-dependent immune responses in dendritic cells in infection and inflammation by stabilizing UBC13.; Authors - Floriana Mulas
human	WB	Cell Mol Immunol; Virus-inducible IGFALS facilitates innate immune responses by mediating IRAK1 and TRAF6 activation.; Authors - Gang Xu
mouse	WB	Mol Cell Proteomics; Quantification of Dynamic Protein Interactions and Phosphorylation in LPS Signaling Pathway by SWATH-MS; Authors - Xiurong Wu

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