Anticorps Polyclonal de lapin anti-IRAK1

• Phare
• Validé par KD/KO

IRAK1 Polyclonal Antibody for WB, IP, IHC, ELISA, IF/ICC, FC (Intra)

Hôte / Isotype

Lapin / IgG

Réactivité testée

Humain, rat, souris

Applications

WB, IHC, IF/ICC, FC (Intra), IP, RIP, ELISA

Conjugaison

Non conjugué

Publications

32

N° de cat : 10478-2-AP

Synonymes

pelle, IRAK-1, IRAK 1, IRAK, Interleukin-1 receptor-associated kinase 1

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Galerie de données de validation

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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.

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  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.

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  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.

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  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.

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  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.

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  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.

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  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.

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  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).

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  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).

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  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).

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  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).

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  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).

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  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).

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  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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Applications testées

• Résultats positifs en WB: cellules A549, cellules HEK-293, cellules HeLa, cellules Jurkat, cellules K-562, cellules MCF-7, cellules PC-12, cellules PC-13, cellules RAW 264.7
• Résultats positifs en IP: cellules HeLa,
• Résultats positifs en IHC: tissu de cancer du poumon humain, ; il est suggéré de démasquer l'antigène avec un tampon de TE buffer pH 9.0; (*) À défaut, 'le démasquage de l'antigène peut être 'effectué avec un tampon citrate pH 6,0.
• Résultats positifs en IF/ICC: cellules HeLa,
• Résultats positifs en FC (Intra): cellules HeLa,

Dilution recommandée

• Western Blot (WB): WB : 1:500-1:3000
• Immunoprécipitation (IP): IP : 0.5-4.0 ug for 1.0-3.0 mg of total protein lysate
• Immunohistochimie (IHC): IHC : 1:300-1:1200
• Immunofluorescence (IF)/ICC: IF/ICC : 1:50-1:500
• Flow Cytometry (FC) (INTRA): FC (INTRA) : 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

Applications publiées

• KD/KO: See 2 publications below
• WB: See 31 publications below
• IHC: See 6 publications below
• IF: See 2 publications below
• RIP: See 1 publications below

Informations sur le produit

10478-2-AP cible IRAK1 dans les applications de WB, IHC, IF/ICC, FC (Intra), IP, RIP, ELISA et montre une réactivité avec des échantillons Humain, rat, souris

• Réactivité: Humain, rat, souris
• Réactivité citée: rat, Humain, souris
• Hôte / Isotype: Lapin / IgG
• Clonalité: Polyclonal
• Type: Anticorps
• Immunogène: IRAK1 Protéine recombinante Ag0728
• Nom complet: interleukin-1 receptor-associated kinase 1
• Masse moléculaire calculée: 77 kDa
• Poids moléculaire observé: 68-80 kDa
• Numéro d’acquisition GenBank: BC014963
• Symbole du gène: IRAK1
• Identification du gène (NCBI): 3654
• Conjugaison: Non conjugué
• Forme: Liquide
• Méthode de purification: Purification par affinité contre l'antigène
• Tampon de stockage: PBS avec azoture de sodium à 0,02 % et glycérol à 50 % pH 7,3
• Conditions de stockage: Stocker à -20°C. Stable pendant un an après l'expédition. L'aliquotage n'est pas nécessaire pour le stockage à -20^oC Les 20ul contiennent 0,1% de BSA.

Informations générales

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)

Publications

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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