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Anti-Lactate Dehydrogenase antibody
See all Lactate Dehydrogenase products (10) ...
Goat polyclonal to Lactate Dehydrogenase
Assay by immunoelectrophoresis resulted in a single precipitin arc against anti-Goat Serum as well as purified and partially purified Lactate Dehydrogenase [Rabbit Muscle].
IHC-FoFr, WB, ELISA, Conjugation, ICC/IFmore details
Reacts with
Rat, Rabbit, Guinea pig, Human, Potato
Lactate Dehydrogenase [Rabbit Muscle].
purified enzyme from rabbit muscle(Worthington Biochemicals)
Liquid
Store at +4°C short term (1-2 weeks). Aliquot and store at -20°C or -80°C. Avoid repeated freeze / thaw cycles.
0.01M sodium phosphate, 0.14M NaCl, pH 7.4, 0.01% sodium azide
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IgG fraction
This product is an IgG fraction antibody purified from monospecific antiserum by a multi-step process which includes delipidation, salt fractionation and ion exchange chromatography followed by extensive dialysis against the buffer stated above.
Suitable for immunoblotting (western or dot blot), ELISA, conjugation and most immunological methods requiring high titer and specificity.
Polyclonal
IgG
Cancer >> Cancer Metabolism >> Metabolic signaling pathway >> Metabolism of carbohydrates
Cancer >> Tumor biomarkers >> Enzymes >> Lactic Dehydrogenase
Signal Transduction >> Metabolism >> Energy Metabolism
Our Abpromise guarantee covers the use of ab2101 in the following tested applications.
The application notes include recommended starting dilutions; optimal dilutions/concentrations should be determined by the end user.
IHC-FoFr: Use at an assay dependent dilution. (PubMed: 18698340)
WB: 1/1000Predicted molecular weight: 138 kDa.((See reference by Zaman et al and recommended protocol). Predicted molecular weight: 138 kDa under non-reducing conditions and 35 kDa under reducing conditions. )
ELISA: 1/500 - 1/1000.(This product has been assayed against 1.0 ug of Lactate Dehydrogenase [Rabbit Muscle] in a standard sandwich ELISA using Peroxidase conjugated Affinity Purified anti-Goat IgG [H&L] (Rabbit) and (ABTS (2,2'-azino-bis-[3-ethylbenthiazoline-6-sulfonic acid]) as a substrate for 30 minutes at room temperature.)
Conjugation: Use at an assay dependent dilution.
ICC/IF: Use a concentration of 1 µg/ml
Lactate dehydrogenase (LDH) is present in a wide variety of organisms, including plants and animals. It is an oxidoreductase which catalyses the interconversion of pyruvate and lactate with concomitant interconversion of NADH and NAD+. As it can also catalyze the oxidation of hydroxybutyrate, it is occasionally called Hydroxybutyrate Dehydrogenase (HBD). There are 5 different isoenzymes of LDH, LDH1 to LDH5, each composed of 4 subunits which may be of 2 different types - M and H subunits. These subunits are encoded by two different genes: The M subunit is encoded by gene LDHA whilst the H subunit is encoded by LDHB. Usually LDH2 is the predominant form in the serum. An LDH1 level higher than the LDH2 level suggests myocardial infarction (damage to heart tissues releases heart LDH, which is rich in LDH1, into the bloodstream).
Cytoplasmic
Immunohistochemistry (PFA perfusion fixed frozen sections) - Lactate Dehydrogenase antibody (ab2101)

ab2101 staining Lactate Dehydrogenase in rat brain tissue sections by Immunohistochemistry (PFA perfusion fixed frozen sections). Rats were anesthetized and intracardially perfused with 500 ml of normal saline at room temperature, followed by 500 ml of ice-cold, freshly made 4% paraformaldehyde in phosphate buffer (PB, 0.1 M, pH 7.4). Alexa Fluor® 546 conjugated anti goat antibody was used as secondary.
Image from Hashimoto T. et. al., PLoS ONE. 2008; 3(8): e2915 (Fig. 4B)
Immunocytochemistry/ Immunofluorescence-Lactate Dehydrogenase antibody(ab2101)

ICC/IF image of ab2101 stained HeLa cells. The cells were 4% formaldehyde fixed (10 min) and then incubated in 1%BSA / 10% normal donkey serum / 0.3M glycine in 0.1% PBS-Tween for 1h to permeabilise the cells and block non-specific protein-protein interactions. The cells were then incubated with the antibody (ab2101, 1µg/ml) overnight at +4°C. The secondary antibody (green) was Alexa Fluor® 488 donkey anti-goat IgG (H+L) used at a 1/1000 dilution for 1h. Alexa Fluor® 594 WGA was used to label plasma membranes (red) at a 1/200 dilution for 1h. DAPI was used to stain the cell nuclei (blue) at a concentration of 1.43µM.
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ab2101 staining Lactate Dehydrogenase in rat brain tissue sections by Immunohistochemistry (PFA perfusion fixed frozen sections). Rats were anesthetized and intracardially perfused with 500 ml of normal saline at room temperature, followed by 500 ml of ice-cold, freshly made 4% paraformaldehyde in phosphate buffer (PB, 0.1 M, pH 7.4). Alexa Fluor® 546 conjugated anti goat antibody was used as secondary.
Image from Hashimoto T. et. al., PLoS ONE. 2008; 3(8): e2915 (Fig. 4B)

ICC/IF image of ab2101 stained HeLa cells. The cells were 4% formaldehyde fixed (10 min) and then incubated in 1%BSA / 10% normal donkey serum / 0.3M glycine in 0.1% PBS-Tween for 1h to permeabilise the cells and block non-specific protein-protein interactions. The cells were then incubated with the antibody (ab2101, 1µg/ml) overnight at +4°C. The secondary antibody (green) was Alexa Fluor® 488 donkey anti-goat IgG (H+L) used at a 1/1000 dilution for 1h. Alexa Fluor® 594 WGA was used to label plasma membranes (red) at a 1/200 dilution for 1h. DAPI was used to stain the cell nuclei (blue) at a concentration of 1.43µM.
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