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Thermo Fisher Scientific ACY1 Monoclonal Antibody (OTI1E5), TrueMAB
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Thermo Fisher Scientific ACY1 Monoclonal Antibody (OTI1E5), TrueMAB

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Human ACY1 단백질을 인식하는 Mouse monoclonal antibody로 Western blot 및 Flow cytometry에 사용 가능. Lyophilized 형태로 제공되며, PBS buffer에 trehalose 포함. 연구용으로 안정적이며 재구성 후 약 1 mg/mL 농도로 사용 가능.

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마지막 업데이트 2025. 08. 05. 오전 05:49
Thermo Fisher Scientific CF503192 ACY1 Monoclonal Antibody (OTI1E5), TrueMAB 100 ug pk판매 단위 pk ·
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784,000원VAT 포함 862,400원

Thermo Fisher Scientific · Thermo Fisher Scientific ACY1 Monoclonal Antibody (OTI1E5), TrueMAB

Applications

Western Blot (WB)

  • Tested Dilution: 1:2,000

Flow Cytometry (Flow)

  • Tested Dilution: 1:100

Product Specifications

항목 내용
Species Reactivity Human
Host / Isotype Mouse / IgG1
Class Monoclonal
Type Antibody
Clone OTI1E5
Immunogen Full length human recombinant protein of human ACY1 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)

Additional Formats


Product Specific Information

For reconstitution, add 100 µL distilled water to obtain a final antibody concentration of approximately 1 mg/mL.
For conjugation experiments, perform an additional desalting step using Zeba Spin Desalting Columns (7K 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 may function 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 its expression is frequently reduced or undetectable.
Mutations in ACY1 cause aminoacylase-1 deficiency, a metabolic disorder characterized by CNS defects and increased urinary excretion of N-acetylated amino acids.
Alternative splicing results in 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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