Mouse Anti-GATM Recombinant Antibody (CBLG1-2625) (V2LY-1225-LY795)
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Basic Information
| Application | Note |
| WB | 1:2,000 |
| IF(ICC) | 1:100 |
| IHC | 1:150 |
| FC | 1:100 |
Formulations & Storage [For reference only, actual COA shall prevail!]
Target
Creatine metabolic process Source: CAFA
Learning or memory Source: CAFA
Multicellular organism development Source: CAFA
Muscle atrophy Source: CAFA
Positive regulation of cold-induced thermogenesis Source: YuBioLab
Isoform 2: Cytoplasm
An autosomal recessive disorder characterized by developmental delay/regression, mental retardation, severe disturbance of expressive and cognitive speech, and severe depletion of creatine/phosphocreatine in the brain. Most patients develop a myopathy characterized by muscle weakness and atrophy later in life.
Fanconi renotubular syndrome 1 (FRTS1):
A form of Fanconi renotubular syndrome, a disease due to a generalized dysfunction of the proximal kidney tubule resulting in decreased solute and water reabsorption. Patients have polydipsia and polyuria with phosphaturia, glycosuria and aminoaciduria. They may develop hypophosphatemic rickets or osteomalacia, acidosis and a tendency toward dehydration. Some eventually develop renal insufficiency. FRTS1 inheritance is autosomal dominant.
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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)
Proteogenomic
Other Protocols
Alternative Versions
Mouse Anti-GATM Recombinant Antibody (CBLG1-2625) (CAT#: CBMAB-G2332-LY)
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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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