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Thermo Fisher Scientific Aminoacylase Polyclonal Antibody
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Thermo Fisher Scientific Aminoacylase Polyclonal Antibody

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Thermo Fisher Scientific의 Aminoacylase Polyclonal Antibody는 Mouse 유래 단백질을 인식하는 Goat IgG 폴리클로날 항체입니다. Western blot 및 Immunoprecipitation에 적합하며, 높은 특이성과 안정성을 제공합니다. 연구용으로만 사용 가능합니다.

카탈로그번호
PA547371
판매단위
pk
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마지막 업데이트 2025. 08. 05. 오후 07:03
Thermo Fisher Scientific PA547371 Aminoacylase Polyclonal Antibody 100 ug pk판매 단위 pk ·
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921,800원VAT 포함 1,013,980원

Thermo Fisher Scientific · Thermo Fisher Scientific Aminoacylase Polyclonal Antibody

Applications

Application Tested Dilution
Western Blot (WB) 0.1 µg/mL
Immunoprecipitation (IP) 25 µg/mL

Product Specifications

항목 내용
Species Reactivity Mouse
Host / Isotype Goat / IgG
Class Polyclonal
Type Antibody
Immunogen Mouse myeloma cell line NS0-derived recombinant mouse Aminoacylase/ACY1 Met1–Ser408
Conjugate Unconjugated
Form Lyophilized
Concentration 0.2 mg/mL
Purification Antigen affinity chromatography
Storage Buffer PBS with 5% trehalose
Contains No Preservative
Storage Conditions -20°C, Avoid Freeze/Thaw Cycles
Shipping Conditions Ambient (domestic); Wet ice (international)
RRID AB_2605808

Product Specific Information

  • In direct ELISAs and Western blots, approximately 50% cross-reactivity with recombinant human Aminoacylase/ACY1 is observed.
  • Reconstitute at 0.2 mg/mL in sterile PBS.

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 postulated to function in the catabolism and salvage of acylated amino acids.
This gene is located on chromosome 3p21.1, a region reduced to homozygosity in small-cell lung cancer (SCLC), and its expression has been reported to be reduced or undetectable in SCLC cell lines and tumors.
The amino acid sequence of human aminoacylase-1 is highly homologous to the porcine counterpart, and this enzyme is 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 of this gene results in multiple transcript variants. Read-through transcription also exists between this gene and the upstream ABHD14A (abhydrolase domain containing 14A) gene. A related pseudogene has been identified on chromosome 18.


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

제품 이미지

Aminoacylase Antibody Immunogen
Aminoacylase Antibody PDP

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