Neurabin 1 Rabbit Polyclonal Antibody
cat.: HA500169
Product Type: Rabbit polyclonal IgG, primary antibodies
Species reactivity: Human, Mouse, Rat
Applications: WB, IF-Cell, IHC-P, FC
Clonality: Polyclonal
Form: Liquid
Storage condition: Store at +4℃ after thawing. Aliquot store at -20℃. Avoid repeated freeze / thaw cycles.
Storage buffer: 1*TBS (pH7.4), 0.2% BSA, 50% Glycerol. Preservative: 0.05% Sodium Azide.
Concentration: 1ug/ul
Purification: Immunogen affinity purified.
Molecular weight: Predicted band sizes: 123/140/145/154 kDa
Isotype: IgG
Immunogen: Recombinant protein within human Neurabin 1 aa 1-200.
Positive control: Rat brain tissue, SH-SY5Y, human liver carcinoma tissue, mouse brain tissue.
Subcellular location: Cell junction, Cytoplasm, Cytoskeleton, Synapse, Synaptosome.
Recommended Dilutions:
  WB
  IF-Cell
  IHC-P
  FC
1:500-1:1,000
1:50-1:100
1:100-1:500
1:50-1:100
Uniprot #: SwissProt: Q9ULJ8 Human | O35867 Rat | Q7TN74 Mouse
Alternative names: FLJ20068 KIAA1222 NEB1_HUMAN Neurabin I Neurabin-1 Neurabin-I Neurabin1 NeurabinI Neural tissue specific F actin binding protein I Neural tissue-specific F-actin-binding protein I NRB 1 NRB I NRB1 NRBI Ppp1r9a Protein phosphatase 1 regulatory (inhibitor) subunit 9A Protein phosphatase 1 regulatory subunit 9A
Images
HA500169_1.jpg Fig1: Western blot analysis of Neurabin 1 on rat brain tissue lysates. Proteins were transferred to a PVDF membrane and blocked with 5% BSA in PBS for 1 hour at room temperature. The primary antibody (HA500169, 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.
HA500169_2.jpg Fig2: ICC staining of Neurabin 1 in SH-SY5Y cells (green). Formalin fixed cells were permeabilized with 0.1% Triton X-100 in TBS for 10 minutes at room temperature and blocked with 10% negative goat serum for 15 minutes at room temperature. Cells were probed with the primary antibody (HA500169, 1/50) for 1 hour at room temperature, washed with PBS. Alexa Fluor®488 conjugate-Goat anti-Rabbit IgG was used as the secondary antibody at 1/1,000 dilution. The nuclear counter stain is DAPI (blue).
HA500169_3.jpg Fig3: Immunohistochemical analysis of paraffin-embedded rat brain tissue using anti-Neurabin 1 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 (HA500169, 1/400) 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.
HA500169_4.jpg Fig4: Immunohistochemical analysis of paraffin-embedded human liver carcinoma tissue using anti-Neurabin 1 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 (HA500169, 1/400) 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.
HA500169_5.jpg Fig5: Immunohistochemical analysis of paraffin-embedded mouse brain tissue using anti-Neurabin 1 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 (HA500169, 1/400) 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.
HA500169_6.jpg Fig6: Flow cytometric analysis of Neurabin 1 was done on SHSY5Y cells. The cells were fixed, permeabilized and stained with the primary antibody (HA500169, 1/50) (red). After incubation of the primary antibody at room temperature for an hour, the cells were stained with a Alexa Fluor 488-conjugated Goat anti-Rabbit IgG Secondary antibody at 1/1000 dilution for 30 minutes.Unlabelled sample was used as a control (cells without incubation with primary antibody; black).
Note: All products are “FOR RESEARCH USE ONLY AND ARE NOT INTENDED FOR DIAGNOSTIC OR THERAPEUTIC USE”.