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

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Human ACY1 단백질을 인식하는 Rabbit Polyclonal Antibody로, Western Blot 및 Immunohistochemistry에 적합. 항원 친화 크로마토그래피로 정제되었으며, PBS 기반 저장용액에 40% 글리세롤 포함. 연구용으로만 사용 가능.

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마지막 업데이트 2025. 08. 05. 오후 09:48
Thermo Fisher Scientific PA583314 Aminoacylase Polyclonal Antibody 100 ul pk판매 단위 pk ·
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740,000원VAT 포함 814,000원

Thermo Fisher Scientific · Thermo Fisher Scientific Aminoacylase Polyclonal Antibody

Applications

Western Blot (WB)

  • Tested Dilution: 0.04–0.4 µg/mL

Immunohistochemistry (Paraffin) (IHC (P))

  • Tested Dilution: 1:1,000–1:2,500

Product Specifications

항목 내용
Species Reactivity Human
Host / Isotype Rabbit / IgG
Class Polyclonal
Type Antibody
Immunogen Recombinant protein corresponding to Human ACY1. Recombinant protein control fragment (Product #RP-96318).
Conjugate Unconjugated
Form Liquid
Concentration 0.7 mg/mL
Purification Antigen affinity chromatography
Storage Buffer PBS, pH 7.2, with 40% glycerol
Contains 0.02% sodium azide
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_2790470

Product Specific Information

Immunogen sequence:
QGMELFVQRP EFHALRAGFA LDEGIANPTD AFTVFYSERS PWWVRVTSTG RPGHASRFME DTAAEKLHKV VNSILAFRE


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), and its expression is often reduced or undetectable in SCLC cell lines and tumors.
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 this gene 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 exists between this gene and the upstream ABHD14A gene. A related 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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