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Thermo Fisher Scientific ACY1 Monoclonal Antibody (OTI2B5), TrueMAB
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Thermo Fisher Scientific ACY1 Monoclonal Antibody (OTI2B5), TrueMAB

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인간 ACY1 단백질을 인식하는 Mouse IgG2a 단일클론 항체로 Western blot과 유세포분석에 적합. 동결건조 형태로 제공되며, PBS 버퍼에 trehalose 포함. 연구용으로만 사용 가능하며 재구성 및 결합 실험에 적합.

카탈로그번호
CF503191
판매단위
pk
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마지막 업데이트 2025. 08. 04. 오후 03:06
Thermo Fisher Scientific CF503191 ACY1 Monoclonal Antibody (OTI2B5), TrueMAB 100 ug pk판매 단위 pk ·
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784,000원VAT 포함 862,400원

Thermo Fisher Scientific · Thermo Fisher Scientific ACY1 Monoclonal Antibody (OTI2B5), TrueMAB

Thermo Fisher Scientific ACY1 Monoclonal Antibody (OTI2B5), TrueMAB

Applications and Tested Dilution

Application Tested Dilution
Western Blot (WB) 1:2,000
Flow Cytometry (Flow) 1:100

Product Specifications

항목 내용
Species Reactivity Human
Host / Isotype Mouse / IgG2a
Class Monoclonal
Type Antibody
Clone OTI2B5
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

  • Biotin conjugate available (Product # TA700052)
  • Custom conjugation service available

Product Specific Information

For reconstitution, add 100 µL distilled water to achieve a final concentration of approximately 1 mg/mL.
For conjugation experiments, perform an additional desalting step (recommended: 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 is involved in the catabolism and salvage of acylated amino acids.
This gene is located on chromosome 3p21.1, a region associated with small-cell lung cancer (SCLC), where expression is often reduced or undetectable.
Mutations in ACY1 cause aminoacylase-1 deficiency, a metabolic disorder characterized by central nervous system defects and increased urinary excretion of N-acetylated amino acids.
Alternative splicing results in multiple transcript variants, and read-through transcription occurs between ACY1 and ABHD14A. A pseudogene is found on chromosome 18.

For Research Use Only. Not for use in diagnostic procedures. Not for resale without express authorization.

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