
Thermo Fisher Scientific Aminoacylase Monoclonal Antibody (15G2)
Aminoacylase 단백질을 인식하는 Mouse monoclonal antibody(15G2)로, Human, Mouse, Rat 시료에 반응. Western blot, IHC, Flow Cytometry 등에 사용 가능. Protein A 정제, 2 mg/mL 농도, PBS/BSA/glycerol buffer에 보관. 연구용 전용.
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Applications and Tested Dilutions
| Application | Tested Dilution |
|---|---|
| Western Blot (WB) | 1:500–1:1,000 |
| Immunohistochemistry (Paraffin) (IHC (P)) | 1:50–1:200 |
| Flow Cytometry (Flow) | 1:50–1:100 |
Product Specifications
| 항목 | 내용 |
|---|---|
| Species Reactivity | Human, Mouse, Rat |
| Host / Isotype | Mouse / IgG2a |
| Class | Monoclonal |
| Type | Antibody |
| Clone | 15G2 |
| Immunogen | Recombinant protein within Human ACY1 aa 55–256 |
| Conjugate | Unconjugated |
| Form | Liquid |
| Concentration | 2 mg/mL |
| Purification | Protein A |
| Storage buffer | PBS, pH 7.4, with 0.2% BSA, 50% glycerol |
| Contains | 0.05% 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_2897727 |
Product Specific Information
Positive controls:
Rat kidney tissue lysate, human liver tissue lysate, rat liver tissue, human liver tissue, human kidney tissue, mouse small intestine tissue, SHSY5Y.
Target Information
ACY1 encodes a cytosolic, homodimeric, zinc-binding enzyme that catalyzes the hydrolysis of acylated L-amino acids to L-amino acids and an acyl group. It is involved in the catabolism and salvage of acylated amino acids. The gene is located on chromosome 3p21.1, a region often showing loss of heterozygosity in small-cell lung cancer (SCLC), where its expression is reduced or undetectable. The human aminoacylase-1 sequence is highly homologous to the porcine counterpart and represents the first member of a new family of zinc-binding enzymes. Mutations cause aminoacylase-1 deficiency, a metabolic disorder with CNS defects and increased urinary N-acetylated amino acids. Alternative splicing generates multiple transcript variants, and read-through transcription occurs with the upstream ABHD14A gene. A pseudogene exists on chromosome 18.
For Research Use Only. Not for use in diagnostic procedures. Not for resale without express authorization.
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