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Thermo Fisher Scientific Aminoacylase 1 Polyclonal Antibody
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Thermo Fisher Scientific Aminoacylase 1 Polyclonal Antibody

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Aminoacylase 1 단백질을 인식하는 Rabbit Polyclonal Antibody로, WB, IHC, ICC, ELISA 등 다양한 실험에 사용 가능. Human, Mouse, Rat에 반응하며 Protein A로 정제된 1 mg/mL 액상 제품. 연구용으로만 사용.

카탈로그번호
BS-6019R
판매단위
pk
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마지막 업데이트 2025. 08. 05. 오전 03:27
Thermo Fisher Scientific BS-6019R Aminoacylase 1 Polyclonal Antibody 100 ul pk판매 단위 pk ·
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531,800원VAT 포함 584,980원

Thermo Fisher Scientific · Thermo Fisher Scientific Aminoacylase 1 Polyclonal Antibody

Applications and Tested Dilution

Application Tested Dilution
Western Blot (WB) Assay-dependent
Immunohistochemistry (Paraffin) (IHC (P)) Assay-dependent
Immunohistochemistry (Frozen) (IHC (F)) 1:100–1:500
Immunocytochemistry (ICC/IF) 1:50–1:200
ELISA 1:500–1:1,000

Product Specifications

항목 내용
Species Reactivity Human, Mouse, Rat
Host / Isotype Rabbit / IgG
Class Polyclonal
Type Antibody
Immunogen KLH conjugated synthetic peptide derived from human ACY1/Aminoacylase 1, amino acids 201–300
Conjugate Unconjugated
Form Liquid
Concentration 1 mg/mL
Purification Protein A
Storage Buffer 0.01M TBS, pH 7.4, with 50% glycerol, 1% BSA
Contains 0.02% ProClin 300
Storage Conditions -20°C
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 is involved in the catabolism and salvage of acylated amino acids. The gene is located on chromosome 3p21.1, a region associated with small-cell lung cancer (SCLC), where its expression is often reduced or undetectable. The human aminoacylase-1 sequence is highly homologous to the porcine enzyme and represents the first member of a zinc-binding enzyme family. Mutations in this gene cause aminoacylase-1 deficiency, a metabolic disorder with central nervous system defects and increased urinary excretion of N-acetylated amino acids. Alternative splicing and read-through transcription with ABHD14A are known, and a pseudogene exists on chromosome 18.


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

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