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Anti-DVL1 Rabbit Polyclonal Antibody
Anti-DVL1 Rabbit Polyclonal Antibody
Catalog #: 10105-060
Supplier:  Prosci
DVL1 Antibody
Anti-DVL1 Rabbit Polyclonal Antibody
Catalog #: 10105-060
Supplier:  Prosci
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Specifications

  • Antibody type:
    Primary
  • Antigen name:
    dishevelled segment polarity protein 1
  • Clonality:
    Polyclonal
  • Gene ID:
    O14640-2
  • Host:
    Rabbit
  • Reactivity:
    Human
  • Antigen symbol:
    DVL1
  • Conjugation:
    Unconjugated
  • ELISA:
    Yes
  • Size:
    100 ul
  • Western blot:
    Yes
  • Form:
    Liquid
  • Antigen synonyms:
    DVL1
  • Storage buffer:
    Purified antibody supplied in 1x PBS buffer with 0.09% (w/v) sodium azide and 2% sucrose.
  • Molecular weight:
    73 kDa
  • Storage temperature:
    For short periods of storage (days) store at 4 °C. For longer periods of storage, store DVL1 antibody at –20 °C. As with any antibody avoid repeat freeze-thaw cycles.
  • Shipping temperature:
    4 °C
  • Immunogen:
    Antibody produced in rabbits immunized with a synthetic peptide corresponding a region of human DVL1.
  • Purification:
    Antibody is purified by protein A chromatography method.
  • Cat. no.:
    10105-060
  • Supplier No.:
    27-500

Specifications

About this item

DVL1 is a cytoplasmic phosphoprotein that regulates cell proliferation, acting as a transducer molecule for developmental processes, including segmentation and neuroblast specification. DVL1 gene is a candidate for neuroblastomatous transformation. The Schwartz-Jampel syndrome and Charcot-Marie-Tooth disease type 2A have been mapped to the same region as DVL1 gene. The phenotypes of these diseases may be consistent with defects which might be expected from aberrant expression of a DVL gene during development.DVL1, the human homolog of the Drosophila dishevelled gene (dsh) encodes a cytoplasmic phosphoprotein that regulates cell proliferation, acting as a transducer molecule for developmental processes, including segmentation and neuroblast specification. DVL1 is a candidate gene for neuroblastomatous transformation. The Schwartz-Jampel syndrome and Charcot-Marie-Tooth disease type 2A have been mapped to the same region as DVL1. The phenotypes of these diseases may be consistent with defects which might be expected from aberrant expression of a DVL gene during development. Three transcript variants encoding three different isoforms have been found for this gene.

DVL1 antibody can be used for detection of DVL1 by ELISA at 1:62500. DVL1 antibody can be used for detection of DVL1 by western blot at 2.5 ?g/mL, and HRP conjugated secondary antibody should be diluted 1:50,000 - 100,000.

Antibody is purified by protein A chromatography method.

Antibody is lyophilized in PBS buffer with 2% sucrose. Add 100 ?L of distilled water. Final antibody concentration is 1 mg/mL.

Aliquot and store at -20°C or below. Avoid multiple freeze-thaw cycles.

Type: Primary
Antigen: DVL1
Clonality: Polyclonal
Clone:
Conjugation: Unconjugated
Epitope:
Host: Rabbit
Isotype:
Reactivity: Human

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