
Thermo Fisher Scientific GATM Monoclonal Antibody (OTI1E3), TrueMAB
GATM 단백질을 인식하는 Mouse Monoclonal Antibody(OTI1E3)로, WB, IHC, ICC, Flow Cytometry에 적합합니다. 동결건조 형태로 제공되며, 재구성 후 약 1 mg/mL 농도로 사용 가능합니다. 인간 시료 반응성이 있으며 연구용으로 권장됩니다.
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Applications and Tested Dilutions
| Application | Tested Dilution |
|---|---|
| Western Blot (WB) | 1:2,000 |
| Immunohistochemistry (Paraffin) (IHC (P)) | 1:150 |
| Immunocytochemistry (ICC/IF) | 1:100 |
| Flow Cytometry (Flow) | 1:100 |
Product Specifications
| 항목 | 내용 |
|---|---|
| Species Reactivity | Human |
| Host / Isotype | Mouse / IgG2a |
| Class | Monoclonal |
| Type | Antibody |
| Clone | OTI1E3 |
| Immunogen | Full length human recombinant protein of human GATM produced in HEK293T cell |
| Conjugate | Unconjugated |
| Form | Lyophilized |
| Concentration | 1 mg/mL |
| Purification | Affinity chromatography |
| Storage Buffer | PBS, pH 7.3, with 8% trehalose |
| Contains | No preservative |
| Storage Conditions | -20°C, Avoid Freeze/Thaw Cycles |
| Shipping Conditions | Ambient (domestic); Wet ice (international) |
Product Specific Information
For reconstitution, add 100 µL of distilled water to obtain a final antibody concentration of approximately 1 mg/mL.
When using this carrier-free antibody for conjugation experiments, perform an additional desalting step (e.g., Zeba Spin Desalting Columns, 7K MWCO, 0.5 mL, Product #89882).
Target Information
AGAT, also known as glycine amidinotransferase (L-arginine:glycine amidinotransferase), GATM, or transamidinase, is a 423 amino acid protein belonging to the amidinotransferase family.
Encoded by a gene located on human chromosome 15q21.1, AGAT exists as three alternatively spliced isoforms and typically forms a homodimer.
AGAT localizes to mitochondrial inner and peripheral membranes as well as the cytoplasm. It is expressed in various tissues including brain, heart, liver, lung, salivary gland, skeletal muscle, and kidney.
AGAT is involved in the biosynthesis of guanidinoacetate, a precursor of creatine, which is essential for energy metabolism in muscle tissues.
Defects in AGAT are associated with arginine:glycine amidinotransferase deficiency, an autosomal recessive disorder characterized by developmental delay, mental retardation, and severe depletion of creatine/phosphocreatine in the brain.
AGAT may play roles in embryonic and central nervous system development and in cardiac response during heart failure by elevating local creatine synthesis.
For Research Use Only. Not for use in diagnostic procedures. Not for resale without express authorization.
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