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Thermo Fisher Scientific Aminoacylase Monoclonal Antibody (OTI2D3)
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Thermo Fisher Scientific Aminoacylase Monoclonal Antibody (OTI2D3)

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Thermo Fisher Scientific의 Aminoacylase 단클론 항체(OTI2D3)는 Western blot, IHC, Flow cytometry에 사용 가능하며 인간, 마우스, 랫트, 개에 반응합니다. HEK293 세포에서 생산된 전체 길이 인간 ACY1 단백질을 항원으로 사용하며, 액상 형태로 제공되어 안정적인 단백질 검출에 적합합니다.

카탈로그번호
MA525618
판매단위
pk
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마지막 업데이트 2025. 08. 02. 오후 01:09
Thermo Fisher Scientific MA525618 Aminoacylase Monoclonal Antibody (OTI2D3) 100 ul pk판매 단위 pk ·
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775,200원VAT 포함 852,720원

Thermo Fisher Scientific · Thermo Fisher Scientific Aminoacylase Monoclonal Antibody (OTI2D3)

Applications and Tested Dilution

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

Product Specifications

Specification Description
Species Reactivity Dog, Human, Mouse, Rat
Host / Isotype Mouse / IgG1
Class Monoclonal
Type Antibody
Clone OTI2D3
Immunogen Full length human recombinant protein of ACY1 produced in HEK293 cell
Conjugate Unconjugated
Form Liquid
Concentration 0.29 mg/mL
Purification Affinity Chromatography
Storage Buffer PBS, pH 7.3, 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)
RRID AB_2722864

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 catabolism and salvage of acylated amino acids. The gene is located on chromosome 3p21.1, a region often reduced to homozygosity in small-cell lung cancer (SCLC), where expression may be reduced or undetectable.

The human aminoacylase-1 sequence is highly homologous to the porcine counterpart and represents the first member of a new family of zinc-binding enzymes. 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 is located on chromosome 18.

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

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