Anticorps Recombinant de lapin anti-SAE1

SAE1 Recombinant Antibody for IHC, IF/ICC, FC (Intra), ELISA

Hôte / Isotype

Lapin / IgG

Réactivité testée

Humain

Applications

IHC, IF/ICC, FC (Intra), ELISA

Conjugaison

Non conjugué

CloneNo.

241923F12

N° de cat : 84516-6-RR

Synonymes

241923F12, AOS1, HSPC140, Sentrin/SUMO activating protein AOS1, SUA1

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Galerie de données de validation

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  IHC staining of human colon cancer using 84516-6-RR

  Immunohistochemical analysis of paraffin-embedded human colon cancer tissue slide using 84516-6-RR (SAE1 antibody) at dilution of 1:600 (under 20x lens). Heat mediated antigen retrieval with Tris-EDTA buffer (pH 9.0).

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  IHC staining of human colon cancer using 84516-6-RR

  Immunohistochemical analysis of paraffin-embedded human colon cancer tissue slide using 84516-6-RR (SAE1 antibody) at dilution of 1:600 (under 20x lens). Heat mediated antigen retrieval with Tris-EDTA buffer (pH 9.0).

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  IF Staining of HeLa using 84516-6-RR

  Immunofluorescent analysis of (4% PFA) fixed HeLa cells using SAE1 antibody (84516-6-RR, Clone: 241923F12 ) at dilution of 1:500 and CoraLite®488-Conjugated Goat Anti-Rabbit IgG(H+L) (SA00013-2), CL594-Phalloidin (red).

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  IF Staining of MCF-7 using 84516-6-RR

  Immunofluorescent analysis of (4% PFA) fixed MCF-7 cells using SAE1 antibody (84516-6-RR, Clone: 241923F12 ) at dilution of 1:500 and CoraLite®488-Conjugated Goat Anti-Rabbit IgG(H+L) (SA00013-2), CL594-Phalloidin (red).

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  FC experiment of A549 using 84516-6-RR

  1x10^6 A549 cells were intracellularly stained with 0.25 ug SAE1 Recombinant antibody (84516-6-RR, Clone:241923F12) and CoraLite®488-Conjugated Goat Anti-Rabbit IgG(H+L) (SA00013-2)(red), or 0.25 ug Rabbit IgG Isotype Control RecAb (98136-1-RR, Clone: 240953C9) (blue). Cells were fixed and permeabilized with Transcription Factor Staining Buffer Kit (PF00011).

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  Affinity and Kinetic Characterization of 84516-6-RR

  Biolayer interferometry (BLl) kinetic assays of 84516-6-RR against Human SAE1 were performed. The affinity constant is 1.52 nM.

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Applications testées

• Résultats positifs en IHC: tissu de cancer du côlon 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 MCF-7, cellules HeLa
• Résultats positifs en FC (Intra): cellules A549,

Dilution recommandée

• Immunohistochimie (IHC): IHC : 1:300-1:1200
• Immunofluorescence (IF)/ICC: IF/ICC : 1:250-1:1000
• Flow Cytometry (FC) (INTRA): FC (INTRA) : 0.25 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

Informations sur le produit

84516-6-RR cible SAE1 dans les applications de IHC, IF/ICC, FC (Intra), ELISA et montre une réactivité avec des échantillons Humain

• Réactivité: Humain
• Hôte / Isotype: Lapin / IgG
• Clonalité: Recombinant
• Type: Anticorps
• Immunogène: SAE1 Protéine recombinante Ag0275
• Nom complet: SUMO1 activating enzyme subunit 1
• Masse moléculaire calculée: 38 kDa
• Numéro d’acquisition GenBank: BC000344
• Symbole du gène: SAE1
• Identification du gène (NCBI): 10055
• Conjugaison: Non conjugué
• Forme: Liquide
• Méthode de purification: Protein A purfication
• Tampon de stockage: PBS with 0.02% sodium azide and 50% glycerol
• 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

SAE1(SUMO-activating enzyme subunit 1) is also named as AOS1, SUA1, UBLE1A and belongs to the ubiquitin-activating E1 family. SAE1 has a calculated molecular mass of 38 kD. SAE1 and UBA2 form a heterodimer that functions as a SUMO-activating enzyme for the sumoylation of proteins(PMID:9920803). Western blot analysis of synchronized HeLa cells detectes increased AOS1 expression as cells progressed through S phase, followed by a substantial decrease in G2 phase. Immunofluorescence analysis shows AOS1 and UBA2 distributed throughout nuclei, but they are excluded from nucleoli.(PMID:11481243).

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