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Thermo Fisher Scientific Aminoacylase Monoclonal Antibody (15G2)
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Thermo Fisher Scientific Aminoacylase Monoclonal Antibody (15G2)

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Aminoacylase 단백질을 인식하는 Mouse monoclonal antibody(15G2)로, Human, Mouse, Rat 시료에 반응. Western blot, IHC, Flow Cytometry 등에 사용 가능. Protein A 정제, 2 mg/mL 농도, PBS/BSA/glycerol buffer에 보관. 연구용 전용.

카탈로그번호
MA537803
판매단위
pk
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마지막 업데이트 2025. 08. 04. 오후 09:10
Thermo Fisher Scientific MA537803 Aminoacylase Monoclonal Antibody (15G2) 100 ul pk판매 단위 pk ·
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655,000원VAT 포함 720,500원

Thermo Fisher Scientific · Thermo Fisher Scientific Aminoacylase Monoclonal Antibody (15G2)

Applications and Tested Dilutions

Application Tested Dilution
Western Blot (WB) 1:500–1:1,000
Immunohistochemistry (Paraffin) (IHC (P)) 1:50–1:200
Flow Cytometry (Flow) 1:50–1:100

Product Specifications

항목 내용
Species Reactivity Human, Mouse, Rat
Host / Isotype Mouse / IgG2a
Class Monoclonal
Type Antibody
Clone 15G2
Immunogen Recombinant protein within Human ACY1 aa 55–256
Conjugate Unconjugated
Form Liquid
Concentration 2 mg/mL
Purification Protein A
Storage buffer PBS, pH 7.4, with 0.2% BSA, 50% glycerol
Contains 0.05% sodium azide
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_2897727

Product Specific Information

Positive controls:
Rat kidney tissue lysate, human liver tissue lysate, rat liver tissue, human liver tissue, human kidney tissue, mouse small intestine tissue, SHSY5Y.

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 often showing loss of heterozygosity in small-cell lung cancer (SCLC), where its expression is 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 cause aminoacylase-1 deficiency, a metabolic disorder with CNS defects and increased urinary N-acetylated amino acids. Alternative splicing generates multiple transcript variants, and read-through transcription occurs with the upstream ABHD14A gene. 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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