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Full length protein
Amino Acid Sequence
Our Abpromise guarantee covers the use of
in the following tested applications.
The application notes include recommended starting dilutions; optimal dilutions/concentrations should be determined by the end user.
Stability and Storage
Shipped at 4°C. Store at +4°C. Do Not Freeze.
Constituents: 0.32% Tris HCl, 0.0292% EDTA, 41% Ammonium sulphate, 0.015% DTT
This product is an active protein and may elicit a biological response in vivo, handle with caution.
- Cell proliferation-inducing gene 19 protein
- L lactate dehydrogenase B chain
Fermentation; pyruvate fermentation to lactate; (S)-lactate from pyruvate: step 1/1.
Involvement in disease
Defects in LDHA are the cause of glycogen storage disease type 11 (GSD11) [MIM:612933]. A metabolic disorder that results in exertional myoglobinuria, pain, cramps and easy fatigue.
Belongs to the LDH/MDH superfamily. LDH family.
Information by UniProt
has not yet been referenced specifically in any publications.
Please note: All products are "FOR RESEARCH USE ONLY AND ARE NOT INTENDED FOR DIAGNOSTIC OR THERAPEUTIC USE"