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Thermo Fisher Scientific ACY1 Monoclonal Antibody (OTI1D4), TrueMAB
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Thermo Fisher Scientific ACY1 Monoclonal Antibody (OTI1D4), TrueMAB

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Thermo Fisher Scientific의 ACY1 단클론 항체(OTI1D4)는 인간 및 생쥐 시료에 반응하며 Western blot, IHC, Flow cytometry에 적합합니다. 고순도 친화 크로마토그래피 정제, 동결건조 형태로 제공되며 연구용으로 사용됩니다.

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마지막 업데이트 2025. 08. 05. 오전 09:48
Thermo Fisher Scientific CF503189 ACY1 Monoclonal Antibody (OTI1D4), TrueMAB 100 ug pk판매 단위 pk ·
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784,000원VAT 포함 862,400원

Thermo Fisher Scientific · Thermo Fisher Scientific ACY1 Monoclonal Antibody (OTI1D4), TrueMAB

Thermo Fisher Scientific ACY1 Monoclonal Antibody (OTI1D4), TrueMAB

Applications and Tested Dilution

Application Tested Dilution
Western Blot (WB) 1:500–1:2,000
Immunohistochemistry (Paraffin) (IHC (P)) 1:150
Flow Cytometry (Flow) 1:100

Product Specifications

Property Description
Species Reactivity Human, Mouse
Host / Isotype Mouse / IgG1
Class Monoclonal
Type Antibody
Clone OTI1D4
Immunogen Full length human recombinant protein of human ACY1 produced in HEK293 cells
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 using this carrier-free antibody, 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 hydrolysis of acylated L-amino acids to L-amino acids and acyl groups. It is involved in catabolism and salvage of acylated amino acids.
The gene is located on chromosome 3p21.1, a region associated with small-cell lung cancer (SCLC), where its expression is often 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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(이미지 파일: CF503189_Aminoacylase_Q03154-1_House_mouse.svg, CF503189_Aminoacylase_Q03154-1_House_mouse_PDP.jpeg)

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