AP21335BT-N LDH1/2 H4/H3M Isozyme antibody

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1 ml / €360.00
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Rabbit anti Human LDH1/2 H4/H3M Isozyme


Product Description for LDH1/2 H4/H3M Isozyme

Rabbit anti Human LDH1/2 H4/H3M Isozyme.
Presentation: Biotin
Product is tested for Dot blot, Enzyme Immunoassay, Immunodiffusion, Immunocytochemistry/Immunofluorescence, Immunoprecipitation, Radioimmunoassay, Western blot / Immunoblot.

Properties for LDH1/2 H4/H3M Isozyme

Product Category Primary Antibodies
Quantity 1 ml
Synonyms L-Lactic dehydrogenase LDH-1 Isozyme H4, L-Lactic dehydrogenase LDH-2 Isozyme H3M
Presentation Biotin
Reactivity Hu
Applications Dot, E, ICC/IF, ID, IP, R, WB
Clonality Polyclonal
Host Rabbit
Isotype IgG
Shipping to Worldwide
PDF datasheet View Datasheet
Manufacturer Acris Antibodies GmbH
Material safety datasheet MSDS for Polyclonal Antibodies (de)

Datasheet Extract

L-Lactic Dehydrogenase, LDH-1(H4)/LDH-2(H3M) isoenzyme, is isolated and purified from Human placenta.
Freund’s complete adjuvant is used in the first step of the immunization
Application This product is intended for use in precipitating and non-precipitating antibody-binding assays (such as e.g., ELISA and Western blotting and Immunofluorescence or Histochemical techniques), to prepare an insoluble immuno-affinity adsorbent, for labelling with a marker of choice.
Working Dilutions:
Non-precipitating antibody-binding techniques: Up to 1/2,000.
Concentration 10.0 mg/ml
Storage Store the antibody lyophilized at 2-8°C and reconstituted at 2-8°C for one week or (in aliquots) at -20°C for longer.
If a slight precipitation occurs upon storage, this should be removed by centrifugation.
Shelf life: one year from despatch.
Molar radio:
Biotin/IgG~ 6.9
Ammonium Sulphate Precipitation and Ion Exchange Chromatography
Buffer System:
PBS, pH 7.2 without preservatives and foreign proteins
Lyophilized hyperimmune IgG fraction
Restore by adding 1.0 ml of sterile distilled water
The antibody recognizes LDH-1(H4)/LDH-2(H3M) isoenzyme, is isolated and purified from Human placenta.
The reagents were evaluated for potency, purity and specificity using most or all of the following techniques: Immunoelectrophoresis, Cross-Immunoelectrophoresis, Single Radial Immunodiffusion (Ouchterlony), block titration, ELISA, Immunoblotting and enzyme inhibition.
Cross-reactivities against enzymes of other sources may occur but have not been determined.

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