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Thermo Fisher Scientific ACY1 Monoclonal Antibody (OTI1H9), TrueMAB
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Thermo Fisher Scientific ACY1 Monoclonal Antibody (OTI1H9), TrueMAB

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Thermo Fisher의 ACY1 단클론 항체(OTI1H9)는 인간 ACY1 단백질을 표적으로 하는 Mouse IgG1 항체입니다. Western blot 및 유세포 분석에 적합하며, 고순도의 액상 형태로 제공됩니다. 연구용으로만 사용 가능하며, 장기 보관 시 -20°C에서 보관합니다.

카탈로그번호
TA503250
판매단위
pk
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마지막 업데이트 2025. 08. 05. 오후 03:31
Thermo Fisher Scientific TA503250 ACY1 Monoclonal Antibody (OTI1H9), TrueMAB 100 ul pk판매 단위 pk ·
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600,200원VAT 포함 660,220원

Thermo Fisher Scientific · Thermo Fisher Scientific ACY1 Monoclonal Antibody (OTI1H9), 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 / IgG1
Class Monoclonal
Type Antibody
Clone OTI1H9
Immunogen Full length human recombinant protein of human ACY1 produced in HEK293T cell
Conjugate Unconjugated
Form Liquid
Concentration 1 mg/mL
Purification Affinity chromatography
Storage Buffer PBS with 1% BSA, 50% glycerol
Contains 0.02% sodium azide
Storage Conditions -20°C, Avoid Freeze/Thaw Cycles
Shipping Conditions Ambient (domestic); Wet ice (international)

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 functions 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 typically reduced or undetectable.
The amino acid sequence of human aminoacylase-1 is highly homologous to the porcine counterpart and represents the first member of a new family of zinc-binding enzymes.
Mutations in this gene cause aminoacylase-1 deficiency, a metabolic disorder characterized by central nervous system defects and increased urinary excretion of N-acetylated amino acids.
Alternative splicing produces multiple transcript variants, and read-through transcription occurs between this gene and the upstream ABHD14A gene. A related 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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