PIPA581310

Aminoacylase Polyclonal Antibody, Invitrogen™

Manufacturer: Thermo Scientific

Select a Size

Pack Size SKU Availability Price
Each of 1 PIPA581310-Each-of-1 In Stock ₹ 32,307.00

PIPA581310 - Each of 1

₹ 32,307.00

In Stock

Quantity

1

Base Price: ₹ 32,307.00

GST (18%): ₹ 5,815.26

Total Price: ₹ 38,122.26

Antigen

Aminoacylase

Classification

Polyclonal

Formulation

PBS with no preservative

Gene Accession No.

Q99JW2

Gene Symbols

ACY1

Immunogen

Recombinant Mouse Aminoacylase-1/ACY1 Protein (Met1-Ser408)

Quantity

100 μL

Primary or Secondary

Primary

Target Species

Mouse

Product Type

Antibody

Isotype

IgG

Applications

ELISA, Immunohistochemistry (Paraffin), Immunoprecipitation, Western Blot

Conjugate

Unconjugated

Gene

ACY1

Gene Alias

1110014J22Rik; ACY IA; ACY IB; ACY1; ACY-1; Acy1a; ACY-1A; Acy1b; ACY-1B; ACY1D; acylase; aminoacylase 1; aminoacylase I; aminoacylase-1; Aminoacylase-1A; aminoacylase-1B; epididymis secretory protein Li 5; HEL-S-5; N-acylamino acid aminohydrolase (Aminoacylase 1); N-acyl-L-amino-acid amidohydrolase

Host Species

Rabbit

Purification Method

Antigen affinity chromatography, Protein A

Regulatory Status

RUO

Gene ID (Entrez)

109652

Content And Storage

Store at 4°C short term. For long term storage, store at -20°C, avoiding freeze/thaw cycles.

Form

Liquid

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Description

  • This product is preservative free
  • It is recommended to add sodium azide to avoid contamination (final concentration 0.05%-0.1%)
  • This antibody has specificity for Mouse Aminoacylase-1/ACY1
  • 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.