Background:

MT-ATP6 (Mitochondrially Encoded ATP Synthase 6) is a Protein Coding gene. Diseases associated with MT-ATP6 include Neuropathy, Ataxia, And Retinitis Pigmentosa and Myopathy, Lactic Acidosis, And Sideroblastic Anemia 3. Among its related pathways are Metabolism and Respiratory electron transport, ATP synthesis by chemiosmotic coupling, and heat production by uncoupling proteins.

Alternative names:

N/A

Clonality:

Polyclonal

Reactivity:

Human

Source:

Rabbit

Isotype:

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Immunogen:

Synthesized peptide derived from human protein . at AA range； 60-140

Concentration:

1mg/ml

Applications:

WB, ELISA

Recommende dilutions:

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Storage:

PBS with 0.02% sodium azide and 50% glycerol pH 7.4. Store at -20°C. Avoid repeated freeze-thaw cycles.

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