DYNLL1 Recombinant Rabbit Monoclonal Antibody [SD08-04]
cat.: ET1612-64
Product Type: Recombinant Rabbit monoclonal IgG, primary antibodies
Species reactivity: Human, Mouse, Rat
Applications: WB, ICC/IF, IHC-P, IP
Clonality: Monoclonal
Clone number: SD08-04
Form: Liquid
Storage condition: Store at +4℃ after thawing. Aliquot store at -20℃ or -80℃. Avoid repeated freeze / thaw cycles.
Storage buffer: 1*TBS (pH7.4), 0.05% BSA, 40% Glycerol. Preservative: 0.05% Sodium Azide.
Concentration: 1 mg/mL.
Purification: Protein A affinity purified.
Molecular weight: 10 kDa
Isotype: IgG
Immunogen: Synthetic peptide within Human DYNLL1 aa 1-50 / 89.
Positive control: MCF-7 cell lysates, Hela, HepG2, 293T, mouse liver tissue, rat esophagus tissue.
Subcellular location: Mitochondrion, Nucleus, centrosome, cytoskeleton.
Recommended Dilutions:
  WB
  ICC/IF
  IHC-P
  IP

1:500-1:2,000
1:50-1:200
1:50-1:200
Use at an assay dependent concentration.
Uniprot #: SwissProt: P63167 Human | P63168 Mouse | P63170 Rat
Alternative names: 8 kDa dynein light chain 8kDLC Cytoplasmic dynein light polypeptide DLC1 DLC8 DNCL1 DNCLC1 DYL1_HUMAN Dynein , cytoplasmic, light chain 1 Dynein light chain 1 cytoplasmic Dynein light chain 1, cytoplasmic Dynein light chain LC8 type 1 Dynein light chain LC8-type 1 Dynein, cytoplasmic, light polypeptide 1 Dynein, light chain, LC8-type 1 DYNLL1 HDLC1 LC8 LC8a MGC126137 MGC126138 MGC72986 PIN Protein inhibitor of neuronal nitric oxide synthase Protein inhibitor of neuronal NOS
Images
ET1612-64_1.jpg Fig1: Western blot analysis of DYNLL1 on MCF-7 cell lysates. Proteins were transferred to a PVDF membrane and blocked with 5% BSA in PBS for 1 hour at room temperature. The primary antibody (ET1612-64, 1/500) was used in 5% BSA at room temperature for 2 hours. Goat Anti-Rabbit IgG - HRP Secondary Antibody (HA1001) at 1:5,000 dilution was used for 1 hour at room temperature.
ET1612-64_2.jpg Fig2: ICC staining of DYNLL1 in Hela cells (green). Formalin fixed cells were permeabilized with 0.1% Triton X-100 in TBS for 10 minutes at room temperature and blocked with 1% Blocker BSA for 15 minutes at room temperature. Cells were probed with the primary antibody (ET1612-64, 1/50) for 1 hour at room temperature, washed with PBS. Alexa Fluor®488 Goat anti-Rabbit IgG was used as the secondary antibody at 1/1,000 dilution. The nuclear counter stain is DAPI (blue).
ET1612-64_3.jpg Fig3: ICC staining of DYNLL1 in HepG2 cells (green). Formalin fixed cells were permeabilized with 0.1% Triton X-100 in TBS for 10 minutes at room temperature and blocked with 1% Blocker BSA for 15 minutes at room temperature. Cells were probed with the primary antibody (ET1612-64, 1/50) for 1 hour at room temperature, washed with PBS. Alexa Fluor®488 Goat anti-Rabbit IgG was used as the secondary antibody at 1/1,000 dilution. The nuclear counter stain is DAPI (blue).
ET1612-64_4.jpg Fig4: ICC staining of DYNLL1 in 293T cells (green). Formalin fixed cells were permeabilized with 0.1% Triton X-100 in TBS for 10 minutes at room temperature and blocked with 1% Blocker BSA for 15 minutes at room temperature. Cells were probed with the primary antibody (ET1612-64, 1/50) for 1 hour at room temperature, washed with PBS. Alexa Fluor®488 Goat anti-Rabbit IgG was used as the secondary antibody at 1/1,000 dilution. The nuclear counter stain is DAPI (blue).
ET1612-64_5.jpg Fig5: Immunohistochemical analysis of paraffin-embedded mouse liver tissue using anti-DYNLL1 antibody. The section was pre-treated using heat mediated antigen retrieval with Tris-EDTA buffer (pH 8.0-8.4) for 20 minutes.The tissues were blocked in 5% BSA for 30 minutes at room temperature, washed with ddH2O and PBS, and then probed with the primary antibody (ET1612-64, 1/50) for 30 minutes at room temperature. The detection was performed using an HRP conjugated compact polymer system. DAB was used as the chromogen. Tissues were counterstained with hematoxylin and mounted with DPX.
ET1612-64_6.jpg Fig6: Immunohistochemical analysis of paraffin-embedded rat esophagus tissue using anti-DYNLL1 antibody. The section was pre-treated using heat mediated antigen retrieval with Tris-EDTA buffer (pH 8.0-8.4) for 20 minutes.The tissues were blocked in 5% BSA for 30 minutes at room temperature, washed with ddH2O and PBS, and then probed with the primary antibody (ET1612-64, 1/50) for 30 minutes at room temperature. The detection was performed using an HRP conjugated compact polymer system. DAB was used as the chromogen. Tissues were counterstained with hematoxylin and mounted with DPX.
Note: All products are “FOR RESEARCH USE ONLY AND ARE NOT INTENDED FOR DIAGNOSTIC OR THERAPEUTIC USE”.