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Validation Data Gallery

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  • Immunofluorescence (IF) / fluorescent staining of Vero cells using dsRNA Recombinant antibody (85780-2-RR)

    IF Staining of Vero using 85780-2-RR (same clone as 85780-2-PBS)

    Immunofluorescent analysis of (4% PFA) fixed Live vaccines of TGEV and PEDV-infected Vero cells using dsRNA antibody (85780-2-RR, Clone: 250708A2 ) at dilution of 1:250 and CoraLite®488-Conjugated Goat Anti-Rabbit IgG(H+L) (SA00013-2). This data was developed using the same antibody clone with 85780-2-PBS in a different storage buffer formulation.

  • Immunofluorescence (IF) / fluorescent staining of Transfected Vero using dsRNA Recombinant antibody (85780-2-RR)

    IF Staining of Transfected Vero using 85780-2-RR (same clone as 85780-2-PBS)

    Immunofluorescent analysis of (4% PFA) fixed Transfected Vero using dsRNA antibody (85780-2-RR, Clone: 250708A2 ) at dilution of 1:250 and CoraLite®488-Conjugated Goat Anti-Rabbit IgG(H+L) (SA00013-2), CL594-Phalloidin (red). This data was developed using the same antibody clone with 85780-2-PBS in a different storage buffer formulation.

  • Flow cytometry (FC) experiment of Transfected Vero using dsRNA Recombinant antibody (85780-2-RR)

    FC experiment of Transfected Vero using 85780-2-RR (same clone as 85780-2-PBS)

    1x10^6 Transfected Vero were intracellularly stained with 0.25 ug dsRNA Recombinant antibody (85780-2-RR, Clone:250708A2) and CoraLite®488-Conjugated Goat Anti-Rabbit IgG(H+L) (SA00013-2), and 0.25 ug Rabbit IgG Isotype Control RecAb (98136-1-RR, Clone: 240953C9). Cells were fixed with 4% PFA and permeabilized with Flow Cytometry Perm Buffer (PF00011-C). This data was developed using the same antibody clone with 85780-2-PBS in a different storage buffer formulation.

  • Dot Blot experiment using dsRNA Recombinant antibody (85780-2-RR)

    Dot Blot experiment using 85780-2-RR (same clone as 85780-2-PBS)

    Dot blot analysis was used to confirm the specificity of 85780-2-RR anti-dsRNA antibody. samples were spotted onto NC and probed with antibody at 5 µg/ml.The amount of sample (μg) spotted is indicated next to each row. This data was developed using the same antibody clone with 85780-2-PBS in a different storage buffer formulation.

  • Dot Blot experiment of Poly(I:C) using dsRNA Recombinant antibody (85780-2-RR)

    Dot Blot experiment of Poly(I:C) using 85780-2-RR (same clone as 85780-2-PBS)

    Dot blot analysis was used to confirm the specificity of 85780-2-RR dsRNA antibody. samples were spotted onto NC and probed with antibody at 1 µg/ml.The amount of sample (μg/mL) spotted is indicated next to each row. This data was developed using the same antibody clone with 85780-2-PBS in a different storage buffer formulation.

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dsRNA Recombinant antibody, PBS Only

dsRNA Uni-rAbTM Recombinant Antibody for IF/ICC, FC (Intra), Dot Blot, Indirect ELISA
Cat No. 85780-2-PBS
Clone No.250708A2

Host / Isotype

Rabbit / IgG

Reactivity

n/a

Applications

IF/ICC, FC (Intra), Dot Blot, Indirect ELISA

Synonyms

250708A2

Formulation:  PBS Only
PBS and Azide
PBS Only
Conjugate:  Unconjugated
Size/Concentration: 

-/ -

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Tested Applications

Recommended dilution

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

Product Information

85780-2-PBS targets dsRNA in IF/ICC, FC (Intra), Dot Blot, Indirect ELISA applications and shows reactivity with n/a samples.

Tested Reactivity n/a
Host / Isotype Rabbit / IgG
Class Recombinant
Type Antibody
Immunogen Peptide 相同性解析による交差性が予測される生物種
Full Name dsRNA
Gene Symbol
Gene ID (NCBI)
Conjugate Unconjugated
Form Liquid
Purification MethodProtein A purification
Storage Buffer PBS only{{ptg:BufferTemp}}7.3
Storage ConditionsStore at -80°C.

Background Information

dsRNA is formed by the base pairing of two RNA strands, creating a double helix structure similar to DNA, but with some differences. dsRNA can be generated through various mechanisms. In the context of viral infections, it can be derived from the genomes of dsRNA viruses, replication intermediates of single-stranded RNA viruses, or bidirectional transcription of certain DNA viruses. Additionally, aberrant splicing or transcriptional processes may lead to the formation of dsRNA structures. dsRNA is recognized as a pathogen-associated molecular pattern (PAMP) by the immune system. It can trigger a series of immune responses in cells, including the activation of antiviral innate immune pathways.