Mouse Anti-SLC25A20 Recombinant Antibody (CBXS-5503) (CBMAB-S2712-CQ)

Basic Information
Formulations & Storage [For reference only, actual COA shall prevail!]
Target
Biological Process carnitine transmembrane transportISS:UniProtKB
Biological Process in utero embryonic developmentIEA:Ensembl
Biological Process mitochondrial transportManual Assertion Based On ExperimentIBA:GO_Central
A rare long-chain fatty acid oxidation disorder. Metabolic consequences include hypoketotic hypoglycemia under fasting conditions, hyperammonemia, elevated creatine kinase and transaminases, dicarboxylic aciduria, very low free carnitine and abnormal acylcarnitine profile with marked elevation of the long-chain acylcarnitines. Clinical features include neurologic abnormalities, cardiomyopathy, arrhythmias, skeletal muscle damage, liver dysfunction and episodes of life-threatening coma, which eventually lead to death. Most patients become symptomatic in the neonatal period with a rapidly progressive deterioration and a high mortality rate.
Helical: 13-31
Mitochondrial matrix: 32-73
Helical: 74-93
Cytoplasmic: 94-112
Helical: 113-131
Mitochondrial matrix: 132-170
Helical: 171-190
Cytoplasmic: 191-211
Helical: 212-230
Mitochondrial matrix: 231-267
Helical: 268-287
Cytoplasmic: 288-301
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Please try the standard protocols which include: protocols, troubleshooting and guide.
Enzyme-linked Immunosorbent Assay (ELISA)
Flow Cytometry
Immunofluorescence (IF)
Immunohistochemistry (IHC)
Immunoprecipitation (IP)
Western Blot (WB)
Enzyme-Linked Immunospot (ELISpot)
Proteogenomics
Other Protocols
Custom Antibody Labeling
We also offer labeled antibodies developed using our catalog antibody products and nonfluorescent conjugates (HRP, AP, Biotin, etc.) or fluorescent conjugates (Alexa Fluor, FITC, TRITC, Rhodamine, Texas Red, R-PE, APC, Qdot Probes, Pacific Dyes, etc.).
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