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Anti-ZIP13 Rabbit Polyclonal Antibody
Anti-ZIP13 Rabbit Polyclonal Antibody
Catalog #: 89417-706
Supplier:  Prosci
Antibody ZIP13 0.1MG
Anti-ZIP13 Rabbit Polyclonal Antibody
Catalog #: 89417-706
Supplier:  Prosci
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Specifications

  • Antibody type:
    Primary
  • Antigen name:
    solute carrier family 39 (zinc transporter), member 13
  • Clonality:
    Polyclonal
  • Gene ID:
    Q96H72
  • Host:
    Rabbit
  • Isotype:
    IgG
  • Reactivity:
    Human
  • Antigen symbol:
    Slc39a13
  • Conjugation:
    Unconjugated
  • ELISA:
    Yes
  • ImmunoChemistry:
    Yes
  • ImmunoFluorescence:
    Yes
  • Size:
    0.1 mg
  • Western blot:
    Yes
  • Form:
    Liquid
  • Antigen synonyms:
    Slc39a13
  • Storage buffer:
    ZIP13 Antibody is supplied in PBS containing 0.02% sodium azide.
  • Storage temperature:
    ZIP13 antibody can be stored at 4 °C for three months and –20 °C, stable for up to one year. As with all antibodies care should be taken to avoid repeated freeze thaw cycles. Antibodies should not be exposed to prolonged high temperatures.
  • Concentration:
    1 mg/mL
  • Shipping temperature:
    4 °C
  • Immunogen:
    ZIP13 antibody was raised against a 14 amino acid synthetic peptide near the amino terminus of human ZIP13. The immunogen is located within amino acids 150 - 200 of ZIP13.
  • Tested applications:
    E, WB, IHC, IF
  • Purification:
    ZIP13 Antibody is affinity chromatography purified via peptide column.
  • Cat. no.:
    89417-706
  • Supplier No.:
    6103

Specifications

About this item

ZIP13 Antibody: The zinc transporter ZIP13, also known as SLC39A13, is a member of a family of divalent ion transporters. Zinc is an essential ion for cells and plays significant roles in the growth, development, and differentiation. The zinc transporter family is divided into four subfamilies (I, II, LIV-1 and gufA). ZIP13 is a multipass membrane protein that belongs to the ZIP transporter subfamily LIV-1. Mutations in ZIP13 have recently been shown to cause a spondylocheiro dysplastic form of Ehlers-Danlos syndrome (SCD-EDS), a generalized skeletal dysplasia involving mainly the spine with clinical abnormalities of the hands in addition to EDS-like features. Other experiments have shown that ZIP13 is required for proper connective tissue development and is involved in BMP/TGF- signaling pathways.

Type: Primary
Antigen: Slc39a13
Clonality: Polyclonal
Clone:
Conjugation: Unconjugated
Epitope:
Host: Rabbit
Isotype: IgG
Reactivity: Human

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