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

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Aminoacylase 1 단백질을 인식하는 Thermo Fisher Scientific의 Rabbit Polyclonal Antibody. Western blot, IHC, ICC/IF에 사용 가능하며, 1 mg/mL 농도의 액상 제품. 인체 반응성, 항원 친화 크로마토그래피로 정제, 연구용 전용.

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마지막 업데이트 2025. 08. 04. 오전 04:50
Thermo Fisher Scientific PA522107 Aminoacylase Polyclonal Antibody 100 ul pk판매 단위 pk ·
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699,000원VAT 포함 768,900원

Thermo Fisher Scientific · Thermo Fisher Scientific Aminoacylase Polyclonal Antibody

Thermo Fisher Scientific Aminoacylase Polyclonal Antibody

Applications and Tested Dilution

Application Tested Dilution
Western Blot (WB) 1:500–1:3,000
Immunohistochemistry (Paraffin) (IHC (P)) 1:100–1:1,000
Immunocytochemistry (ICC/IF) 1:100–1:1,000

Product Specifications

항목 내용
Species Reactivity Human
Host / Isotype Rabbit / IgG
Class Polyclonal
Type Antibody
Immunogen Recombinant fragment corresponding to amino acids 89–366 of Aminoacylase 1 (Uniprot ID# Q03154)
Conjugate Unconjugated
Form Liquid
Concentration 1 mg/mL
Purification Antigen affinity chromatography
Storage Buffer 0.1M Tris glycine, pH 7, with 10% glycerol
Contains 0.01% thimerosal
Storage Conditions Store at 4°C short term. For long term storage, store at -20°C, avoiding freeze/thaw cycles.
Shipping Conditions Wet ice
RRID AB_11151981

Product Specific Information

  • Recommended positive controls: 293T, A431, H1299, HeLa, HepG2, Molt-4, Raji
  • Predicted reactivity: Mouse (85%), Rat (86%), Pig (86%), Bovine (87%)
  • Store product as a concentrated solution. Centrifuge briefly before opening the vial.

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 reduced to homozygosity in small-cell lung cancer (SCLC), where expression is often reduced or undetectable.
Mutations in ACY1 cause aminoacylase-1 deficiency, a metabolic disorder characterized by central nervous system defects and increased urinary excretion of N-acetylated amino acids.
Alternative splicing results in multiple transcript variants; read-through transcription also occurs with the upstream ABHD14A gene. A related pseudogene exists on chromosome 18.

Safety and Regulatory Information

WARNING: This product can expose you to chemicals including mercury, which is known to the State of California to cause birth defects or other reproductive harm.
For more information, visit www.P65Warnings.ca.gov.

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

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