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Anti-LDHB Antibody EP1565Y
Also for LDHB (NM_002300)
|A synthetic peptide corresponding to residues near the N-terminus of human LDH-B was used as an immunogen.|
||Lot dependent; please refer to CoA along with shipment
|WB, IHC, IF, FC
||IHC-Fr: Use at an assay dependent concentration; WB: 1:50000 - 1:200000; IP: 1:100; ICC: 1:100 - 1:250; FC: 1:70; IHC-P: Use at an assay dependent dilution
|PBS 49%,Sodium azide 0.01%,Glycerol 50%,BSA 0.05%|
|Tissue culture supernatant
|Does not react with Mouse, Rat
|Homo sapiens lactate dehydrogenase B (LDHB), transcript variant 1|
|HEL-S-281; LDH-B; LDH-H; LDHBD; TRG-5|
|Lactate dehydrogenase (LDH) is an ubiquitous enzyme commonly found in wide variety of organisms, including plants and microbes. LDH is involved in the interconversion of the pyruvate and NADH to lactate and NAD+. It is also called Hydroxybutyrate Dehydrogenase (HBD), because it can catalyze the oxidation of hydroxybutyrate (1). In mammals, three types of LDH subunits (35 kDa) are encoded by the genes Ldh-A, Ldh-B, and Ldh-C. All LDH subunits can combine to form various terameric isoenzymes (140 kDa). Lactate dehydrogenase B (LDH-B, heart subunit, LDH-H) is involved in the conversion of L-lactate and NAD to pryruvate and NADH and it is predominantly localized in the heart tissue. Similar to other LDH subunit, LDH-B is considered to be an important marker for germ cell tumor (2). |
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Western blot - Lactate Dehydrogenase antibody [EP1565Y]; Anti-Lactate Dehydrogenase antibody [EP1565Y] + HeLa cell lysate at 10 µg.Secondary.Goat anti-rabbit HRP .Predicted band size : 37 kDa.Observed band size : 37 kDa.
Immunohistochemistry (Paraffin-embedded sections) - Lactate Dehydrogenase antibody [EP1565Y]; Human heart muscle labelled with TA300979 at 1/100 - 1/250 dilution
Immunocytochemistry/ Immunofluorescence - Anti-Lactate Dehydrogenase antibody [EP1565Y]; ICC/IF image of TA300979 stained HepG2 cells. The cells were 100% methanol fixed (5 min) and then incubated in 1%BSA / 10% normal goat 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 overnight at +4Â°C. The secondary antibody (green) was , DyLight? 488 goat anti-rabbit IgG (H+L) used at a 1/250 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 1.43ÂµM.
Flow Cytometry - Anti-Lactate Dehydrogenase antibody [EP1565Y]; Overlay histogram showing HeLa cells stained with TA300979 (red line). The cells were fixed with 80% methanol (5 min) and then permeabilized with 0.1% PBS-Tween for 20 min. The cells were then incubated in 1x PBS / 10% normal goat serum / 0.3M glycine to block non-specific protein-protein interactions followed by the antibody for 30 min at 22Â°C. The secondary antibody used was DyLight? 488 goat anti-rabbit IgG (H+L) at 1/500 dilution for 30 min at 22Â°C. Isotype control antibody (black line) was rabbit IgG (monoclonal) (1Âµg/1x10^6 cells) used under the same conditions. Acquisition of >5,000 events was performed.