Render Target: STATIC
Render Timestamp: 2024-12-20T11:39:29.006Z
Commit: f2d32940205a64f990b886d724ccee2c9935daff
XML generation date: 2024-10-01 12:01:06.313
Product last modified at: 2024-10-02T07:00:57.311Z
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PDP - Template Name: Monoclonal Antibody
PDP - Template ID: *******c5e4b77
R Recombinant
Recombinant: Superior lot-to-lot consistency, continuous supply, and animal-free manufacturing.

SPTLC1 (F7Y7S) Rabbit mAb #76977

Filter:
  • WB
  • IP

    Supporting Data

    REACTIVITY H
    SENSITIVITY Endogenous
    MW (kDa) 50
    Source/Isotype Rabbit IgG
    Application Key:
    • WB-Western Blotting 
    • IP-Immunoprecipitation 
    Species Cross-Reactivity Key:
    • H-Human 

    Product Information

    Product Usage Information

    Application Dilution
    Western Blotting 1:1000
    Simple Western™ 1:50 - 1:250
    Immunoprecipitation 1:50

    Storage

    Supplied in 10 mM sodium HEPES (pH 7.5), 150 mM NaCl, 100 µg/mL BSA, 50% glycerol, and less than 0.02% sodium azide. Store at –20°C. Do not aliquot the antibody.

    Protocol

    Specificity / Sensitivity

    SPTLC1 (F7Y7S) Rabbit mAb recognizes endogenous levels of total SPTLC1 protein. This antibody does not cross-react with SPTLC2 or SPTLC3 protein.

    Species Reactivity:

    Human

    Source / Purification

    Monoclonal antibody is produced by immunizing animals with a synthetic peptide corresponding to residues surrounding Lys207 of human SPTLC1 protein.

    Background

    The serine palmitoyltransferase (SPT) complex catalyzes the initial and rate-limiting step of de novo sphingolipid biosynthesis. This protein complex consists of an SPTLC1/SPTLC2 heterodimer or an SPTLC1/SPTLC3 heterodimer as the catalytic core (1-3). Studies show that SPTLC1 mutations leading to unregulated SPT activity and increased sphingolipid synthesis cause amyotrophic lateral sclerosis (ALS), a progressive neurodegenerative disease (4). In addition, mutations in SPTLC1 that change the substrate of SPT from serine to alanine drive the accumulation of deoxysphingolipids and cause neuropathy. Furthermore, dietary restriction of serine and glycine also leads to the accumulation of deoxysphingolipids in tumors and reduces tumor growth in mouse xenograft models (5).
    For Research Use Only. Not For Use In Diagnostic Procedures.
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