Render Target: STATIC
Render Timestamp: 2024-11-14T10:36:00.575Z
Commit: 3c1f305a63297e594ac8d7bb5424007d592d68be
XML generation date: 2024-09-30 01:58:51.207
Product last modified at: 2024-09-30T08:00:52.292Z
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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.

DYNLL1/LC8 (E6W7R) Rabbit mAb #82007

Filter:
  • WB

    Supporting Data

    REACTIVITY H M R
    SENSITIVITY Endogenous
    MW (kDa) 10
    Source/Isotype Rabbit IgG
    Application Key:
    • WB-Western Blotting 
    Species Cross-Reactivity Key:
    • H-Human 
    • M-Mouse 
    • R-Rat 

    Product Information

    Product Usage Information

    Application Dilution
    Western Blotting 1:1000

    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

    DYNLL1/LC8 (E6W7R) Rabbit mAb recognizes endogenous levels of total DYNLL1/LC8 protein. This antibody cross-reacts with DYNLL2.

    Species Reactivity:

    Human, Mouse, Rat

    Source / Purification

    Monoclonal antibody is produced by immunizing animals with a synthetic peptide corresponding to residues surrounding Ala28 of human DYNLL1/LC8 protein.

    Background

    Hub proteins are important components of protein interaction networks, binding to a wide variety of proteins, and often driving dimerization (1). The dynein light chain LC8 family members, DYNLL1 and DYNLL2, are conserved, ubiquitously expressed hub proteins that interact with a diverse group of proteins, including molecular motor proteins. LC8 family member protein interactions regulate multiple cellular processes (2).
    Loss of DYNLL1 in BRCA1-mutant cancer cells restores homologous recombination by allowing DNA end resection, conferring resistance to platinum and PARP inhibitor therapies (3).  DYNLL1 regulation of DNA repair pathways likely occurs through its interaction with end resection machinery and 53BP1 (3,4). Upregulation of DYNLL1 has been associated with chemoresistance and progression of human cancer (5-7).
    For Research Use Only. Not For Use In Diagnostic Procedures.
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