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Thermo Fisher Scientific ACY1 Monoclonal Antibody (OTI1B12), TrueMAB
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Thermo Fisher Scientific ACY1 Monoclonal Antibody (OTI1B12), TrueMAB

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ACY1 단백질을 인식하는 Mouse monoclonal 항체로 Western blot, IHC, Flow cytometry에 사용 가능. 사람, 마우스, 랫트, 개에 반응. Lyophilized 형태로 제공되며, PBS buffer와 trehalose 포함. 연구용으로만 사용.

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마지막 업데이트 2025. 08. 04. 오전 11:21
Thermo Fisher Scientific CF503227 ACY1 Monoclonal Antibody (OTI1B12), TrueMAB 100 ug pk판매 단위 pk ·
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784,000원VAT 포함 862,400원

Thermo Fisher Scientific · Thermo Fisher Scientific ACY1 Monoclonal Antibody (OTI1B12), TrueMAB

Applications and Tested Dilutions

Application Tested Dilution
Western Blot (WB) 1:200–1:500
Immunohistochemistry (Paraffin) (IHC (P)) 1:150
Flow Cytometry (Flow) 1:100

Product Specifications

항목 내용
Species Reactivity Dog, Human, Mouse, Rat
Host / Isotype Mouse / IgG1
Class Monoclonal
Type Antibody
Clone OTI1B12
Immunogen Full length human recombinant protein of human ACY1 produced in HEK293 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 distilled water to achieve a final antibody concentration of approximately 1 mg/mL.
For conjugation experiments, perform an additional desalting step (Zeba Spin Desalting Columns, 7 K MWCO, 0.5 mL, Product #89882).

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.
This gene is located on chromosome 3p21.1, a region often reduced to homozygosity in small-cell lung cancer (SCLC), where expression is frequently reduced or undetectable. The human aminoacylase-1 sequence is highly homologous to the porcine counterpart and represents the first member of a zinc-binding enzyme family.
Mutations in ACY1 cause aminoacylase-1 deficiency, a metabolic disorder with CNS defects and increased urinary excretion of N-acetylated amino acids. Alternative splicing produces multiple transcript variants, and read-through transcription occurs with the upstream ABHD14A gene. A related 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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