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CLN1 Polyclonal Antibody
Datasheet   

  • Catalog Number:

    E20-70975

  • Amount:

    100ul

  • Price:

    225$

  • Purification:

    The antibody was affinity-purified from rabbit antiserum by affinity-chromatography using epitope-specific immunogen.

  • Immunogen:

    The antiserum was produced against synthesized peptide derived from human CLN1. AA range:16-65

  • Source:

    Polyclonal, Rabbit

  • Gene Name:

    PPT1

  • Dilution:

    Immunohistochemistry: 1/100 - 1/300. ELISA: 1/10000. Not yet tested in other applications.

  • Immunohistochemistry analysis of CLN1 antibody in paraffin-embedded human prostate carcinoma tissue.

  • Background:

    palmitoyl-protein thioesterase 1(PPT1) Homo sapiens The protein encoded by this gene is a small glycoprotein involved in the catabolism of lipid-modified proteins during lysosomal degradation. The encoded enzyme removes thioester-linked fatty acyl groups such as palmitate from cysteine residues. Defects in this gene are a cause of infantile neuronal ceroid lipofuscinosis 1 (CLN1, or INCL) and neuronal ceroid lipofuscinosis 4 (CLN4). Two transcript variants encoding different isoforms have been found for this gene.[provided by RefSeq, Dec 2008],

  • Protein Name:

    Palmitoyl-protein thioesterase 1

  • Human Gene Id:

    5538

  • Human Swiss Prot No:

    P50897

  • Mouse Gene Id:

    19063

  • Mouse Swiss Prot No:

    O88531

  • Rat Gene Id:

    29411

  • Rat Swiss Prot No:

    P45479

  • Specificity:

    CLN1 Polyclonal Antibody detects endogenous levels of CLN1 protein.

  • Formulation:

    Liquid in PBS containing 50% glycerol, 0.5% BSA and 0.02% sodium azide.

  • Concentration:

    1 mg/ml

  • Storage Stability:

    -20°C/1 year

  • Other Name:

    PPT1; PPT; Palmitoyl-protein thioesterase 1; PPT-1; Palmitoyl-protein hydrolase 1

  • MolecularWeight(Da):

    34193

  • Observed Band(KD):

    37

  • Function:

    catalytic activity:Palmitoyl-protein + H(2)O = palmitate + protein.,disease:Defects in PPT1 are a cause of neuronal ceroid lipofuscinosis 4 (CLN4) [MIM:204300]; also known as adult type neuronal ceroid lipofuscinosis (NCL) or Kufs disease.,disease:Defects in PPT1 are the cause of infantile neuronal ceroid lipofuscinosis 1 (CLN1) [MIM:256730]; also called infantile neuronal ceroid lipofuscinosis (INCL). The neuronal ceroid lipofuscinosis are a group of progressive neurodegenerative diseases characterized by the intracellular accumulation of autofluorescent lipopigment storage material in different patterns ultrastructurally. The lipopigment pattern seen most often in CLN1 is referred to as granular osmiophilic deposits (GROD). There is a core group of four major clinical forms, the infantile, the late-infantile, the juvenile, and the adult forms. The infantile forms are characterized by p

  • Subcellular Location:

    extracellular region,extracellular space,nucleus,lysosome,Golgi apparatus,cytosol,synaptic vesicle,membrane,axon,dendrite,neuronal cell body,lysosomal lumen,membrane raft,extracellular exosome,

  • Expression:

    Brain,Cerebellum,Liver,Prostate,Testis,

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Catalog Number

  • Amount:100ul
  • Price:225$

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