Thermo Fisher Scientific Aminoacylase Recombinant Rabbit Monoclonal Antibody (006), FITC
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카탈로그 번호 | CAS 번호 | 설명 | 상태 | 단위 | 판매가 | 할인가 | 가격(VAT포함) | 수량 / 장바구니 / 찜 |
MA540914 | - | Thermo Fisher Scientific MA540914 Aminoacylase Recombinant Rabbit Monoclonal Antibody (006), FITC 100 tests pk | 재고문의 | pk | 0원 | - | 0원 |
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Applications
Tested Dilution
Publications
Flow Cytometry (Flow)
Assay-Dependent
Product Specifications
Host/Isotype
Rabbit / IgG
Class
Recombinant Monoclonal
Type
Antibody
Clone
006
Immunogen
Recombinant Human ACY1/Aminoacylase-1 protein
Conjugate
FITC FITC FITC
View additional formats
Excitation/Emission Max
498/517 nm View spectra
Form
Liquid
Concentration
0.1 mg/mL
Storage conditions
4° C, store in dark, DO NOT FREEZE!
Shipping conditions
Wet ice
Product Specific Information
May be stored for twelve months without detectable loss of activity. Protect from prolonged exposure to light and do not freeze. Sodium azide is toxic to cells and should be disposed of properly so flush with large volumes of water during disposal.
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, and has been postulated to function 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 has been reported to be 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 this enzyme is the first member of a new family of zinc-binding enzymes. Mutations in this gene cause aminoacylase-1 deficiency, a metabolic disorder characterized by central nervous system defects and increased urinary excretion of N-acetylated amino acids. Alternative splicing of this gene results in multiple transcript variants. Read-through transcription also exists between this gene and the upstream ABHD14A (abhydrolase domain containing 14A) gene. A related pseudogene has been identified on chromosome 18.
For Research Use Only. Not for use in diagnostic procedures. Not for resale without express authorization.
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