FLT4/CEN5q FISH Probe

Catalog # FG0265

Size

Price

Stock

Quantity

Size:100 uL
Price: USD $ 1,288.00
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Contact Info
  • +1-909-264-1399
    +1-909-992-0619
    Toll Free : +1-877-853-6098
  • +1-909-992-3401
Images
QC Test

Hybridization position of the probes on the chromosome.
Note

Hybridization position of the probes on the chromosome.

Hybridization position of the probes on the chromosome.

  • Specification

    Product Description

    Labeled FISH probes for identification of gene amplification using Fluorescent In Situ Hybridization Technique. (Technology).

    Probe 1

    Name: FLT4
    Size: Approximately 160kb
    Fluorophore: Texas Red
    Location: 5q35.3

    Probe 2

    Name: CEN11p
    Size: Approximately 700kb
    Fluorophore: FITC
    Location: 5q11.2

    Origin

    Human

    Source

    Genomic DNA

    Reactivity

    Human

    Form

    Liquid

    Notice

    We strongly recommend the customer to use FFPE FISH PreTreatment Kit 1 (Catalog #: KA2375 or KA2691) for the pretreatment of Formalin-Fixed Paraffin-Embedded (FFPE) tissue sections.

    Regulatory Status

    For research use only (RUO)

    Quality Control Testing

    Representative images of normal human cell (lymphocyte) stain with the dual color FISH probe. The left image is chromosomes at metaphase, and the right image is an interphase nucleus.

    Supplied Product

    DAPI Counterstain (1500 ng/mL ) 125 uL for each 100 uL FISH Probe

    Storage Instruction

    Store at 4°C in the dark.

    Note

    Hybridization position of the probes on the chromosome.

  • Applications

    Fluorescent In Situ Hybridization (Cell)

  • Gene Info — FLT4

    Entrez GeneID

    2324

    Gene Name

    FLT4

    Gene Alias

    FLT41, LMPH1A, PCL, VEGFR3

    Gene Description

    fms-related tyrosine kinase 4

    Omim ID

    136352 153100 602089

    Gene Ontology

    Hyperlink

    Gene Summary

    This gene encodes a tyrosine kinase receptor for vascular endothelial growth factors C and D. The protein is thought to be involved in lymphangiogenesis and maintenance of the lymphatic endothelium. Mutations in this gene cause hereditary lymphedema type IA. [provided by RefSeq

    Other Designations

    soluble VEGFR3 variant 1|soluble VEGFR3 variant 2|soluble VEGFR3 variant 3|vascular endothelial growth factor receptor 3

  • Interactome
  • Pathway
  • Disease
Contact Info
  • +1-909-264-1399
    +1-909-992-0619
    Toll Free : +1-877-853-6098
  • +1-909-992-3401
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