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Rabbit Anti-LDHA/FITC Conjugated antibody
background:
The protein encoded by this gene catalyzes the conversion of L-lactate and NAD to pyruvate and NADH in the final step of anaerobic glycolysis. The protein is found predominantly in muscle tissue and belongs to the lactate dehydrogenase family. Mutations in this gene have been linked to exertional myoglobinuria. Multiple transcript variants encoding different isoforms have been found for this gene. The human genome contains several non-transcribed pseudogenes of this gene. [provided by RefSeq].
Subunit:
Homotetramer.
Subcellular Location:
Cytoplasm.
Post-translational modifications:
ISGylated.
DISEASE:
Glycogen storage disease 11 (GSD11) [MIM:612933]: A metabolic disorder that results in exertional myoglobinuria, pain, cramps and easy fatigue. Note=The disease is caused by mutations affecting the gene represented in this entry.
Similarity:
Belongs to the LDH/MDH superfamily. LDH family.
Database links:
Entrez Gene: 3939 Human
Entrez Gene: 16828 Mouse
Entrez Gene: 24533 Rat
Omim: 30000 Human
SwissProt: P00338 Human
SwissProt: P06151 Mouse
SwissProt: P04642 Rat
Unigene: 2795 Human
Unigene: 29324 Mouse
Unigene: 107896 Rat
Important Note:
This product as supplied is intended for research use only, not for use in human, therapeutic or diagnostic applications.
乳酸脱氢酶(LD)广泛存在于人体各组织中,以肝、肾、心肌、骨骼肌、胰腺和肺中最多。
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