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

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Rabbit polyclonal antibody specific to human Aminoacylase 1 (ACY1). Suitable for WB, ELISA, and IP applications. Preservative-free liquid form with 1 mg/mL concentration. Ideal for research on amino acid metabolism and small-cell lung cancer studies.

카탈로그번호
PA580314
판매단위
pk
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마지막 업데이트 2025. 08. 04. 오후 04:51
Thermo Fisher Scientific PA580314 Aminoacylase Polyclonal Antibody 100 ul pk판매 단위 pk ·
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424,300원VAT 포함 466,730원

Thermo Fisher Scientific · Thermo Fisher Scientific Aminoacylase Polyclonal Antibody

Applications

Western Blot (WB)

  • Tested Dilution: 1:500–1:2,000

ELISA

  • Tested Dilution: 1:5,000–1:10,000

Immunoprecipitation (IP)

  • Tested Dilution: 1–4 µL/mg of lysate

Product Specifications

항목 내용
Species Reactivity Human
Host / Isotype Rabbit / IgG
Class Polyclonal
Type Antibody
Immunogen Recombinant Human ACY1 protein (Met1–Ser408)
Conjugate Unconjugated
Form Liquid
Concentration 1 mg/mL
Purification Protein A, Antigen affinity chromatography
Storage Buffer PBS
Contains No preservative
Storage Conditions Store at 4°C short term. For long term storage, store at -20°C, avoiding freeze/thaw cycles.
Shipping Conditions Ambient (domestic); Wet ice (international)
RRID AB_2787643

Product Specific Information

  • This product is preservative-free. It is recommended to add sodium azide to avoid contamination (final concentration 0.05%–0.1%).
  • This antibody has specificity for Human Aminoacylase 1 (ACY1).

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 may be 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 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 between ACY1 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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