HFE2 293T Cell Transient Overexpression Lysate(Denatured)

Catalog # H00148738-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

HFE2 transfected lysate.

Western Blot
QC Test

Western Blot

Lane 1: HFE2 transfected lysate ( 33.7 KDa)
Lane 2: Non-transfected lysate.

  • Specification

    Transfected Cell Line

    293T

    Plasmid

    pCMV-HFE2 full-length

    Host

    Human

    Theoretical MW (kDa)

    33.7

    Quality Control Testing

    Transient overexpression cell lysate was tested with Anti-HFE2 antibody (H00148738-B01) by Western Blots.

    SDS-PAGE Gel

    HFE2 transfected lysate.

    Western Blot

    Lane 1: HFE2 transfected lysate ( 33.7 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 — HFE2

    Entrez GeneID

    148738

    GeneBank Accession#

    NM_145277.3

    Protein Accession#

    -

    Gene Name

    HFE2

    Gene Alias

    HFE2A, HJV, JH, MGC23953, RGMC

    Gene Description

    hemochromatosis type 2 (juvenile)

    Omim ID

    602390 608374

    Gene Ontology

    Hyperlink

    Gene Summary

    The product of this gene is involved in iron metabolism. It may be a component of the signaling pathway which activates hepcidin or it may act as a modulator of hepcidin expression. It could also represent the cellular receptor for hepcidin. Alternatively spliced transcript variants encoding different isoforms have been identified for this gene. Defects in this gene are the cause of hemochromatosis type 2A, also called juvenile hemochromatosis (JH). JH is an early-onset autosomal recessive disorder due to severe iron overload resulting in hypogonadotrophic hypogonadism, hepatic fibrosis or cirrhosis and cardiomyopathy, occurring typically before age of 30. [provided by RefSeq

    Other Designations

    OTTHUMP00000015582|OTTHUMP00000015583|OTTHUMP00000059680|RGM domain family, member C|hemochromatosis type 2 protein|hemojuvelin

  • 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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