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>   home   >   Products   >   Primary Antibodies   >   Signal Transduction   >   LDHAL6B Antibody (NT)   

LDHAL6B Antibody (NT)

Rabbit Polyclonal Antibody

  • WB - LDHAL6B Antibody (NT) ABV11287
    LDHAL6B Antibody (NT) western blot analysis in K562 cell line lysates (35 μg/lane).This demonstrates the LDHAL6B antibody detected the LDHAL6B protein (arrow).
Product Information
  • Applications Legend:
  • WB=Western Blot
  • IHC=Immunohistochemistry
  • IHC-P=Immunohistochemistry (Paraffin-embedded Sections)
  • IHC-F=Immunohistochemistry (Frozen Sections)
  • IF=Immunofluorescence
  • FC=Flow Cytopmetry
  • IC=Immunochemistry
  • ICC=Immunocytochemistry
  • IP=Immunoprecipitation
  • DB=Dot Blot
  • CHIP=Chromatin Immunoprecipitation
  • FA=Fluorescence Assay
  • IEM=Immunoelectronmicroscopy
  • EIA=Enzyme Immunoassay
Primary Accession Q9BYZ2
Host Rabbit
Clonality Polyclonal
Isotype Rabbit IgG
Calculated MW 41943 Da
Additional Information
Gene ID 92483
Positive Control Western blot: K562 cell line lysates
Application & Usage Western blot: ~1:1000.
Other Names LDHAL6B; LDHAL6; LDHL; L-lactate dehydrogenase A-like 6B
Target/Specificity LDHAL6B
Antibody Form Liquid
Appearance Colorless liquid
Formulation 100 µl of antibody in PBS with 0.09% (W/V) sodium azide
Handling The antibody solution should be gently mixed before use.
Reconstitution & Storage -20 °C
Background Descriptions
PrecautionsLDHAL6B Antibody (NT) is for research use only and not for use in diagnostic or therapeutic procedures.
Protein Information
Synonyms LDHAL6, LDHL
Tissue Location Testis specific.
Research Areas
Citations (0)

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L-Lactate dehydrogenase A chain (LDHA) is a member of the LDH/MDH superfamily and LDH family. It catalyzes the conversion of L-lactate and NAD to pyruvate and NADH in the final step of anaerobic glycolysis. LDHA is localized primarily in muscle tissue and is part of the lactate dehydrogenase family. Mutations in LDHA have been linked to exertional myoglobinuria. LDH1 is decreased in essential thrombocythemia. LDHA is induced through a non-genomic pathway of estrogen action. Reduction in LDH-A activity results in stimulation of mitochondrial respiration and decrease of mitochondrial membrane potential. Mutations in LDHA have been associated with in LDHA are the cause of glycogen storage disease type 11 (GSD11) which is a metabolic disorder that results in exertional myoglobinuria, pain, cramps and easy fatigue.

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$ 245.00
Cat# ABV11287
(40 western blots)
Availability: 5-7days
Bulk Size
Seasonal Special on Bulk Order
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