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KIF4A antibody [N1N2], N-term

GTX115759
GeneTex
ApplicationsImmunoFluorescence, Western Blot, ImmunoCytoChemistry, ImmunoHistoChemistry, ImmunoHistoChemistry Paraffin
Product group Antibodies
ReactivityHuman
TargetKIF4A
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Overview

  • Supplier
    GeneTex
  • Product Name
    KIF4A antibody [N1N2], N-term
  • Delivery Days Customer
    9
  • Application Supplier Note
    WB: 1:500-1:3000. ICC/IF: 1:100-1:1000. IHC-P: 1:100-1:1000. *Optimal dilutions/concentrations should be determined by the researcher.Not tested in other applications.
  • Applications
    ImmunoFluorescence, Western Blot, ImmunoCytoChemistry, ImmunoHistoChemistry, ImmunoHistoChemistry Paraffin
  • Certification
    Research Use Only
  • Clonality
    Polyclonal
  • Concentration
    1 mg/ml
  • Conjugate
    Unconjugated
  • Gene ID24137
  • Target name
    KIF4A
  • Target description
    kinesin family member 4A
  • Target synonyms
    chromokinesin-A; chromosome-associated kinesin KIF4A; KIF4; KIF4G1; MRX100; XLID100
  • Host
    Rabbit
  • Isotype
    IgG
  • Protein IDO95239
  • Protein Name
    Chromosome-associated kinesin KIF4A
  • Scientific Description
    Kinesins, such as KIF4A, are microtubule-based motor proteins that generate directional movement along microtubules. They are involved in many crucial cellular processes, including cell division (Zhu and Jiang, 2005 [PubMed 15625105]).[supplied by OMIM]
  • Reactivity
    Human
  • Storage Instruction
    -20°C or -80°C,2°C to 8°C
  • UNSPSC
    12352203

References

  • KIF4A promotes tumor progression of bladder cancer via CXCL5 dependent myeloid-derived suppressor cells recruitment. Lin N et al., 2022 Apr 10, Sci Rep
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  • PRR14L mutations are associated with chromosome 22 acquired uniparental disomy, age-related clonal hematopoiesis and myeloid neoplasia. Chase A et al., 2019 May, Leukemia
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  • Kif4A mediate the accumulation and reeducation of THP-1 derived macrophages via regulation of CCL2-CCR2 expression in crosstalking with OSCC. Zhang Y et al., 2017 May 22, Sci Rep
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  • Fucoidan reduced the invasion of oral squamous cell carcinoma cells and modified their effects to macrophages. Lin J et al., 2017 Jan, Med Oncol
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