ASAH1 HEK293 Cell Transient Overexpression Lysate(Non-Denatured)

Catalog # L146T6

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Size:100 ug
Price: USD $ 247.00
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Contact Info
  • +1-909-264-1399
    +1-909-992-0619
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  • +1-909-992-3401
Images
SDS-PAGE Gel
QC Test

SDS-PAGE Gel

ASAH1 transfected lysate

Western Blot
QC Test

Western Blot

Lane 1: ASAH1 transfected lysate ( 45 KDa).
Lane 2: Non-transfected lysate.

  • Specification

    Transfected Cell Line

    HEK293

    Plasmid

    pCMV-ASAH1 full length

    Host

    Human

    Theoretical MW (kDa)

    45

    Lysis Buffer

    Modified RIPA Lysis Buffer:50 mM Tris-HCl pH 7.4, 150 mM NaCl, 1mM EDTA, 1% Triton X-100, 0.1% SDS, 1% Sodium deoxycholate, 1mM PMSF.

    Concentration

    2 mg/ml

    Quality Control Testing

    Transient overexpression cell lysate was tested with Anti-ASAH1 antibody (H00000427-M01 ) by Western Blots.

    SDS-PAGE Gel

    ASAH1 transfected lysate

    Western Blot

    Lane 1: ASAH1 transfected lysate ( 45 KDa).
    Lane 2: Non-transfected lysate.

    Recommend Usage

    Use it directly for immuno-precipitation, or heat lysate with SDS gel loading buffer to 95°C for 5 minutes followed by rapid cooling for western blot application. If dissociating conditions are required, add reducing agent prior to heating.

    Storage Buffer

    In modified RIPA Lysis Buffer.

    Storage Instruction

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

  • Applications

    Western Blot

    Immunoprecipitation

  • Gene Info — ASAH1

    Entrez GeneID

    427

    GeneBank Accession#

    NM_177924

    Protein Accession#

    NP_808592

    Gene Name

    ASAH1

    Gene Alias

    AC, ASAH, FLJ21558, FLJ22079, PHP, PHP32

    Gene Description

    N-acylsphingosine amidohydrolase (acid ceramidase) 1

    Omim ID

    228000

    Gene Ontology

    Hyperlink

    Gene Summary

    This gene encodes a heterodimeric protein consisting of a nonglycosylated alpha subunit and a glycosylated beta subunit that is cleaved to the mature enzyme posttranslationally. The encoded protein catalyzes the synthesis and degradation of ceramide into sphingosine and fatty acid. Mutations in this gene have been associated with a lysosomal storage disorder known as Farber disease. Multiple transcript variants encoding several distinct isoforms have been identified for this gene. [provided by RefSeq

    Other Designations

    N-acylsphingosine amidohydrolase 1|OTTHUMP00000122482|acylsphingosine deacylase|putative 32 kDa heart protein

  • 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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