Anticorps Monoclonal anti-HRD1/SYVN1

• Phare
• Validé par KD/KO

HRD1/SYVN1 Monoclonal Antibody for WB, IHC, IF/ICC, ELISA

Hôte / Isotype

Mouse / IgG2b

Réactivité testée

Humain, rat, souris

Applications

WB, IHC, IF/ICC, ELISA

Conjugaison

Non conjugué

CloneNo.

2C8A7

N° de cat : 67488-1-PBS

Synonymes

SYVN1, 2C8A7, EC:2.3.2.27, HRD1, KIAA1810

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Galerie de données de validation

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  WB analysis using 67488-1-Ig (same clone as 67488-1-PBS)

  Various lysates were subjected to SDS PAGE followed by western blot with 67488-1-Ig (HRD1/SYVN1 antibody) at dilution of 1:20000 incubated at room temperature for 1.5 hours. This data was developed using the same antibody clone with 67488-1-PBS in a different storage buffer formulation.

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  WB analysis of NIH/3T3 using 67488-1-Ig (same clone as 67488-1-PBS)

  NIH/3T3 cells were subjected to SDS PAGE followed by western blot with 67488-1-Ig (HRD1/SYVN1 antibody) at dilution of 1:20000 incubated at room temperature for 1.5 hours. This data was developed using the same antibody clone with 67488-1-PBS in a different storage buffer formulation.

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  WB analysis of 4T1 using 67488-1-Ig (same clone as 67488-1-PBS)

  4T1 cells were subjected to SDS PAGE followed by western blot with 67488-1-Ig (HRD1/SYVN1 antibody) at dilution of 1:20000 incubated at room temperature for 1.5 hours. This data was developed using the same antibody clone with 67488-1-PBS in a different storage buffer formulation.

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  WB analysis of HeLa using 67488-1-Ig (same clone as 67488-1-PBS)

  WB result of HRD1/SYVN1 antibody (67488-1-Ig; 1:2000; incubated at room temperature for 1.5 hours) with sh-Control and sh-HRD1/SYVN1 transfected HeLa cells. This data was developed using the same antibody clone with 67488-1-PBS in a different storage buffer formulation.

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  IHC staining of human liver cancer using 67488-1-Ig (same clone as 67488-1-PBS)

  Immunohistochemical analysis of paraffin-embedded human liver cancer tissue slide using 67488-1-Ig (HRD1/SYVN1 antibody) at dilution of 1:1000 (under 10x lens). Heat mediated antigen retrieval with Tris-EDTA buffer (pH 9.0). This data was developed using the same antibody clone with 67488-1-PBS in a different storage buffer formulation.

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  IHC staining of human liver cancer using 67488-1-Ig (same clone as 67488-1-PBS)

  Immunohistochemical analysis of paraffin-embedded human liver cancer tissue slide using 67488-1-Ig (HRD1/SYVN1 antibody) at dilution of 1:1000 (under 40x lens). Heat mediated antigen retrieval with Tris-EDTA buffer (pH 9.0). This data was developed using the same antibody clone with 67488-1-PBS in a different storage buffer formulation.

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  IF Staining of HeLa using 67488-1-Ig (same clone as 67488-1-PBS)

  Immunofluorescent analysis of (4% PFA) fixed HeLa cells using HRD1/SYVN1 antibody (67488-1-Ig, Clone: 2C8A7 ) at dilution of 1:400 and CoraLite®488-Conjugated AffiniPure Goat Anti-Mouse IgG(H+L). This data was developed using the same antibody clone with 67488-1-PBS in a different storage buffer formulation.

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Informations sur le produit

67488-1-PBS cible HRD1/SYVN1 dans les applications de WB, IHC, IF/ICC, ELISA et montre une réactivité avec des échantillons Humain, rat, souris

• Réactivité: Humain, rat, souris
• Hôte / Isotype: Mouse / IgG2b
• Clonalité: Monoclonal
• Type: Anticorps
• Immunogène: HRD1/SYVN1 Protéine recombinante Ag4456
• Nom complet: synovial apoptosis inhibitor 1, synoviolin
• Masse moléculaire calculée: 617 aa, 68 kDa
• Poids moléculaire observé: 68-76 kDa
• Numéro d’acquisition GenBank: BC030530
• Symbole du gène: HRD1
• Identification du gène (NCBI): 84447
• Conjugaison: Non conjugué
• Forme: Liquide
• Méthode de purification: Purification par protéine A
• Tampon de stockage: PBS only
• Conditions de stockage: Store at -80°C. 20ul contiennent 0,1% de BSA.

Informations générales

HRD1is also named as SYVN1(Synovial apoptosis inhibitor 1) , KIAA1810. It acts as an E3 ubiquitin-protein ligase which accepts ubiquitin specifically from endoplasmic reticulum-associated UBC7 E2 ligase and transfers it to substrates, promoting their degradation. Two distinct binding sites mediate Hrd1 dimerization or oligomerization, one located within the transmembrane region and another within the cytosolic domain. (PMID:19864457).Western blot analysis detected abundant HRD1 expression in liver and kidney. Mouse liver and spleen expressed Hrd1 as an 85-kD protein(PMID:12646171).

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