FANCM 293T Cell Transient Overexpression Lysate(Denatured)

Catalog # H00057697-T01

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Size:100 uL
Price: USD $ 247.00
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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
SDS-PAGE Gel
QC Test

SDS-PAGE Gel

FANCM transfected lysate.

Western Blot
QC Test

Western Blot

Lane 1: FANCM transfected lysate ( 73.7 KDa)
Lane 2: Non-transfected lysate.

  • Specification

    Transfected Cell Line

    293T

    Plasmid

    pCMV-FANCM full-length

    Host

    Human

    Theoretical MW (kDa)

    73.7

    Interspecies Antigen Sequence

    Mouse (82)

    Quality Control Testing

    Transient overexpression cell lysate was tested with Anti-FANCM antibody (H00057697-B01) by Western Blots.

    SDS-PAGE Gel

    FANCM transfected lysate.

    Western Blot

    Lane 1: FANCM transfected lysate ( 73.7 KDa)
    Lane 2: Non-transfected lysate.

    Storage Buffer

    1X Sample Buffer (50 mM Tris-HCl, 2% SDS, 10% glycerol, 300 mM 2-mercaptoethanol, 0.01% Bromophenol blue)

    Storage Instruction

    Store at -80°C. Aliquot to avoid repeated freezing and thawing.

  • Applications

    Western Blot

  • Gene Info — FANCM

    Entrez GeneID

    57697

    GeneBank Accession#

    BC036056.1

    Protein Accession#

    AAH36056.1

    Gene Name

    FANCM

    Gene Alias

    FAAP250, KIAA1596, MGC176453

    Gene Description

    Fanconi anemia, complementation group M

    Omim ID

    609644

    Gene Ontology

    Hyperlink

    Gene Summary

    The Fanconi anemia complementation group (FANC) currently includes FANCA, FANCB, FANCC, FANCD1 (also called BRCA2), FANCD2, FANCE, FANCF, FANCG, FANCI, FANCJ (also called BRIP1), FANCL, FANCM and FANCN (also called PALB2). The previously defined group FANCH is the same as FANCA. Fanconi anemia is a genetically heterogeneous recessive disorder characterized by cytogenetic instability, hypersensitivity to DNA crosslinking agents, increased chromosomal breakage, and defective DNA repair. The members of the Fanconi anemia complementation group do not share sequence similarity; they are related by their assembly into a common nuclear protein complex. This gene encodes the protein for complementation group M. [provided by RefSeq

    Other Designations

    -

  • Interactome
  • 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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