
Thermo Fisher Scientific GATM Polyclonal Antibody
Thermo Fisher Scientific의 GATM Polyclonal Antibody는 인간 GATM 단백질을 인식하는 Rabbit IgG 기반 항체입니다. WB 및 IHC(P) 실험에 적합하며, KLH 결합 합성 펩타이드로 면역화되었습니다. Protein A 및 항원 친화 크로마토그래피로 정제되어 높은 특이성과 재현성을 제공합니다.
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Applications
| Application | Tested Dilution |
|---|---|
| Western Blot (WB) | 1:1,000 |
| Immunohistochemistry (Paraffin) (IHC (P)) | 1:10–1:50 |
Product Specifications
| 항목 | 내용 |
|---|---|
| Species Reactivity | Human |
| Host/Isotype | Rabbit / IgG |
| Class | Polyclonal |
| Type | Antibody |
| Immunogen | KLH conjugated synthetic peptide between 58–84 amino acids from the N-terminal region of human GATM |
| Conjugate | Unconjugated |
| Form | Liquid |
| Purification | Protein A, Antigen affinity chromatography |
| Storage buffer | PBS, pH 7.4 |
| Contains | 0.09% sodium azide |
| Storage conditions | Store at 4°C short term. For long term storage, store at -20°C, avoiding freeze/thaw cycles. |
| Shipping conditions | Ambient (domestic); Wet ice (international) |
| RRID | AB_2541446 |
Product Specific Information
This antibody is predicted to react with bovine, chicken, mouse, porcine, non-human primate, rat, and zebrafish based on sequence homology.
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 that maps to human chromosome 15q21.1, AGAT exists as three alternatively spliced isoforms and consists of a homodimer, with equilibrium between monomeric and dimeric forms favoring a monomer subunit structure.
AGAT localizes to mitochondrial inner membranes, peripheral membranes, and cytoplasm. It is biallelically expressed in placenta and fetal tissues, and also expressed in brain, heart, liver, lung, salivary gland, and skeletal muscle tissue, with high expression in kidney.
AGAT is elevated in the myocardium during heart failure and decreased in inter-uterine growth restriction (IUGR)-associated placenta.
AGAT catalyzes biosynthesis of guanidinoacetate, the immediate precursor of creatine, which plays a vital role in energy metabolism in muscle tissues.
Defects in AGAT are associated with arginine:glycine amidinotransferase deficiency, an autosomal recessive disorder characterized by developmental delay or regression, mental retardation, severe disturbance of expressive and cognitive speech, and severe depletion of creatine/phosphocreatine in brain.
AGAT may be linked to embryonic and central nervous system development and may function in heart failure response 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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