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The image on the left is immunohistochemistry of paraffin-embedded Human gastic cancer tissue using CSB-PA196351(ACP6 Antibody) at dilution 1/50, on the right is treated with fusion protein. (Original magnification: x200)
The image on the left is immunohistochemistry of paraffin-embedded Human gastic cancer tissue using CSB-PA196351(ACP6 Antibody) at dilution 1/50, on the right is treated with fusion protein. (Original magnification: x200)
The image on the left is immunohistochemistry of paraffin-embedded Human gastic cancer tissue using CSB-PA196351(ACP6 Antibody) at dilution 1/50, on the right is treated with fusion protein. (Original magnification: x200)

ACP6 Antibody

CSB-PA196351
Cusabio
ApplicationsELISA, ImmunoHistoChemistry
Product group Antibodies
TargetACP6
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Overview

  • Supplier
    Cusabio
  • Product Name
    ACP6 Antibody
  • Delivery Days Customer
    20
  • Applications
    ELISA, ImmunoHistoChemistry
  • Certification
    Research Use Only
  • Clonality
    Polyclonal
  • Conjugate
    Unconjugated
  • Gene ID51205
  • Target name
    ACP6
  • Target description
    acid phosphatase 6, lysophosphatidic
  • Target synonyms
    acid phosphatase-like protein 1; ACPL1; LPAP; lysophosphatidic acid phosphatase type 6; PACPL1
  • Host
    Rabbit
  • Isotype
    IgG
  • Protein IDQ9NPH0
  • Protein Name
    Lysophosphatidic acid phosphatase type 6
  • Scientific Description
    Lysophosphatidic acid phosphatase type 6 (ACP6), also designated acid phosphatase-like protein 1 (ACPL1) or lysophosphatidic acid phosphatase (LPAP), is a 428 amino acid secreted protein that hydrolyzes lysophosphatidic acid to monoacylglycerol. ACP6 is highly expressed in kidney, heart, small intestine, muscle, liver, prostate, testis, ovary and exists as two isoforms as a result of alternative splicing events. The gene encoding ACP6 maps to human chromosome 1, the largest human chromosome spanning about 260 million base pairs and making up 8% of the human genome. Notably, the rare aging disease Hutchinson-Gilford progeria is associated with the LMNA gene of human chromosome 1, which encodes lamin A. Stickler syndrome, Parkinsons, Gaucher disease, familial adenomatous polyposis and Usher syndrome are also associated with chromosome 1. Aberrations in chromosome 1 are found in a variety of cancers including head and neck cancer, malignant melanoma and multiple myeloma.
  • Storage Instruction
    -20°C or -80°C
  • UNSPSC
    12352203

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