SLC9A3R1 293T Cell Transient Overexpression Lysate(Denatured)

Catalog # H00009368-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

SLC9A3R1 transfected lysate.

Western Blot
QC Test

Western Blot

Lane 1: SLC9A3R1 transfected lysate ( 38.9 KDa)
Lane 2: Non-transfected lysate.

  • Specification

    Transfected Cell Line

    293T

    Plasmid

    pCMV-SLC9A3R1 full-length

    Host

    Human

    Theoretical MW (kDa)

    38.9

    Interspecies Antigen Sequence

    Mouse (86); Rat (87)

    Quality Control Testing

    Transient overexpression cell lysate was tested with Anti-SLC9A3R1 antibody (H00009368-B01) by Western Blots.

    SDS-PAGE Gel

    SLC9A3R1 transfected lysate.

    Western Blot

    Lane 1: SLC9A3R1 transfected lysate ( 38.9 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 — SLC9A3R1

    Entrez GeneID

    9368

    GeneBank Accession#

    NM_004252

    Protein Accession#

    NP_004243

    Gene Name

    SLC9A3R1

    Gene Alias

    EBP50, NHERF, NHERF1, NPHLOP2

    Gene Description

    solute carrier family 9 (sodium/hydrogen exchanger), member 3 regulator 1

    Omim ID

    604990

    Gene Ontology

    Hyperlink

    Gene Summary

    This gene encodes a sodium/hydrogen exchanger regulatory cofactor. The protein interacts with and regulates various proteins including the cystic fibrosis transmembrane conductance regulator and G-protein coupled receptors such as the beta2-adrenergic receptor and the parathyroid hormone 1 receptor. The protein also interacts with proteins that function as linkers between integral membrane and cytoskeletal proteins. The protein localizes to actin-rich structures including membrane ruffles, microvilli, and filopodia. Mutations in this gene result in hypophosphatemic nephrolithiasis/osteoporosis type 2, and loss of heterozygosity of this gene is implicated in breast cancer

    Other Designations

    sodium/hydrogen exchanger regulatory factor 1|solute carrier family 9 (sodium/hydrogen exchanger), isoform 3 regulatory factor 1

  • 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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