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Scicons Mouse double-stranded RNA (K1) Antibody

Scicons Mouse double-stranded RNA (K1) Antibody

Product Specifications

Product Name Alternative

Mouse anti dsRNA

Clonality

Monoclonal

Clone

K1

Conjugation

Unconjugated

Source

Female DBA/2 mice were injected intraperitonially with a mixture of 50 ug L-dsRNA and 75 ug methylated bovine serum albumin, emulsified in complete Freund's adjuvant. After several boosts spleen cells were fused with Sp2/0-Agl4 myeloma cells to generate the hybridoma clone.

Field of Research

Microbiology

Purification

Affinity chromatography on Protein A-agarose.

Concentration

Concentration after reconstitution: 1.00 mg/ml as determined by A280 nm (A280 nm = 1.47 corresponds to 1 mg/ml antibody) .

Purity

Gel electrophoretically pure IgG antibody.

Form

The lyophilised sample should be reconstituted with 200 μl sterile distilled water. The mAb will then be in PBS without any stabilisers or preservatives at a concentration of 1 mgr/ml. As a result of the lyophilisation procedure, the reconstituted antibody may contain small amounts of denatured protein in the form of aggregates that may interfere with some applications such as immunohistochemistry (e.g. by giving high backgrounds) . We therefore highly recommend centrifuging (microcentrifuge) the reconstituted antibody before use and using the supernatant.

Storage Conditions

After reconstitution antibodies should be aliquoted and stored at -20 °C or -70 °C. After adding 10 mM sodium azide undiluted antibody can also be stored at +4 °C for a short period of time. For long term storage the mAb should be kept frozen. Repeated freezing/thawing cycles should be avoided. When kept lyophilized the product will remain stable for 10 years at -20 °C or -70°C.

Notes

For research use only.

Applications Notes

MAb K1 can be used for ELISA, dsRNA-immunoblotting, immuno-affinity-chromatography and in certain systems also for immunohistochemistry (see references) . The optimum working dilution of the antibody for any specific application should be established by titration. Please note that nucleic acid separation prior to dsRNA-immunoblotting must be carried out by polyacrylamide gel electrophoresis, because the sensitivity of detection is considerably lower after blotting from agarose gels. Not for use for clinical purposes. For in vitro use only.

Tested Applications

ELISA, FC, IAC, IB, ICC, IHC, WB

Host or Source

Mouse

Isotype

IgG2a kappa

Frequently Asked Questions

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