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3-hyrdoxybutyrate dehydrogenase

218 €

AS09 562 | clonality: polyclonal | host: rabbit | reactivity: Rhodobacter sphaeroides (Rhodopseudomonas sphaeroides)

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AS09 562

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product information
Background

3-hydroxybutyrate dehydrogenase (EC=1.1.1.30) is an oxidoreductase which participates in synthesis and degradation of ketone bodies and butanoate metabolism. Alternative names: NAD+-beta-hydroxybutyrate dehydrogenase, hydroxybutyrate oxidoreductase, beta-hydroxybutyrate dehydrogenase, D-beta-hydroxybutyrate dehydrogenase, D-3-hydroxybutyrate dehydrogenase, D-(-)-3-hydroxybutyrate dehydrogenase, beta-hydroxybutyric acid dehydrogenase,  -D-hydroxybutyrate dehydrogenase, and beta-hydroxybutyric dehydrogenase.

Immunogen

3-hydroxybutyrate dexydrogenase isolated and purified from Rhodobacter sphaeroides

Host Rabbit
Clonality Polyclonal
Clone
Purity Purified IgG
Format Lyophilized in phosphate buffer saline
Quantity 10 mg
Reconstitution For reconstitution please add 1 ml of sterile destilled water.
Storage

store lyophilized/reconstituted at -20°C; once reconstituted make aliquots to avoid repeated freeze-thaw cycles. Please, remember to spin tubes briefly prior to opening them to avoid any losses that might occur from lyophilized material adhering to the cap or sides of the tubes.

Tested applications western blot (WB), ELISA (ELISA),immunofluorescence (IF), immunohistochemistry (IHC)
Related products

AS09 563 | anti-3-hydroxybutyrate dexydrogenase (biotinylated)

AS09 564 | anti-3-hydroxybutyrate dexydrogenase (affinity purified)

Plant protein extraction buffer

Secondary antibodies

Additional information

antibody potency and purity has been evaluated by immunoelectrophoresis, single radial immunodiffusion (Ouchterlony), ELISA,immunoblotting and enzyme inhibition.

application information
Recommended dilution

1: 100 - 1: 500 for techniques listed above

Expected | apparent MW

26.9 kDa

Confirmed reactivity Rhodopacter shpaeroides
Predicted reactivity

Sagittula stellata, Silicibacter sp.

Not reactive in

no confirmed exceptions from predicted reactivity known in the moment

Additional information

The IgG (7S) fraction is prepared from the antiserum by ammonium sulphate precipitation and ion exchange chromatography.

Selected references

to be added when available



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