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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 Fisher의 Aminoacylase Polyclonal Antibody는 Mouse ACY1 단백질을 인식하는 Rabbit IgG 항체입니다. WB, IHC, ELISA, IP 등 다양한 응용에 사용 가능하며, 보존제가 없는 형태로 제공됩니다. 단기 4°C, 장기 -20°C 보관을 권장합니다.

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마지막 업데이트 2025. 08. 05. 오전 08:09
Thermo Fisher Scientific PA581310 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 and Tested Dilutions

Application Tested Dilution
Western Blot (WB) 1:500–1:1,000
Immunohistochemistry (Paraffin) (IHC-P) 1:2,500–1:10,000
Immunohistochemistry (Frozen) (IHC-F) -
ELISA 1:25,000–1:50,000
Immunoprecipitation (IP) 0.2–1 µL/mg of lysate

Product Specifications

Specification Description
Species Reactivity Mouse
Published Species Mouse
Host / Isotype Rabbit / IgG
Class Polyclonal
Type Antibody
Immunogen Recombinant Mouse Aminoacylase-1/ACY1 Protein (Met1–Ser408)
Conjugate Unconjugated
Form Liquid
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_2788527

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 Mouse 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 is involved in the catabolism and salvage of acylated amino acids.
The gene is located on chromosome 3p21.1, a region reduced to homozygosity in small-cell lung cancer (SCLC). Expression is often reduced or undetectable in SCLC cell lines and tumors.
Human aminoacylase-1 is highly homologous to the porcine counterpart and is the first member of a new family of zinc-binding enzymes.
Mutations cause aminoacylase-1 deficiency, a metabolic disorder with CNS defects and increased urinary excretion of N-acetylated amino acids.
Alternative splicing results in multiple transcript variants, and read-through transcription occurs between this gene and ABHD14A. A 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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