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TAC1 Protein (Fc Tag)

TAC1 Origin: Human Host: HEK-293 Cells Recombinant
Catalog No. ABIN6964372
  • Target See all TAC1 Proteins
    TAC1 (Tachykinin, Precursor 1 (TAC1))
    Protein Type
    Recombinant
    Origin
    Human
    Source
    • 2
    • 1
    HEK-293 Cells
    Purification tag / Conjugate
    This TAC1 protein is labelled with Fc Tag.
    Sequence
    PPT (Arg58-Met107)+hFc(GLU99-ALA330)
    Characteristics
    Tagged Protein: C-Human Fc tag
    Purification
    affinity purification
    Top Product
    Discover our top product TAC1 Protein
  • Application Notes
    Optimal working dilution should be determined by the investigator.
    Restrictions
    For Research Use only
  • Format
    Lyophilized
    Reconstitution
    Reconstitute with deionized water
    Buffer
    Lyophilized from sterile PBS, pH 7.4. Normally 5 % - 8 % trehalose is added as protectants before lyophilization.
    Preservative
    Without preservative
    Storage
    -80 °C
    Storage Comment
    Store at -80°C for 12 months (Avoid repeated freezing and thawing)
    Expiry Date
    12 months
  • Target
    TAC1 (Tachykinin, Precursor 1 (TAC1))
    Alternative Name
    PPT (TAC1 Products)
    Synonyms
    Hs.2563 Protein, NK2 Protein, NKNA Protein, NPK Protein, TAC2 Protein, PPTA3 Protein, Ppt5fl Protein, RATPPTA3 Protein, TAC Protein, TAC1 Protein, 4930528L02Rik Protein, NK-1 Protein, NK1 Protein, Nkna Protein, PPT-A Protein, PPTA Protein, SP Protein, PPT Protein, beta-PPT-A Protein, NKA Protein, nk2 Protein, nkna Protein, npk Protein, tac1 Protein, tac2 Protein, tachykinin Protein, tachykinin precursor 1 Protein, tachykinin, precursor 1 Protein, tachykinin 1 Protein, tachykinin precursor 1 L homeolog Protein, TAC1 Protein, Tac1 Protein, tac1 Protein, tac1.L Protein
    Background
    Synonymes: CLN1, INCL, PPT
    Description: 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]
    Molecular Weight
    30.69 kDa
    UniProt
    P20366
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