Rab9 Recombinant Rabbit Monoclonal Antibody [SR45-05]
cat.: ET1602-29
Product Type: Recombinant Rabbit monoclonal IgG, primary antibodies
Species reactivity: Human, Mouse, Rat
Applications: WB, IF-Cell, IF-Tissue, IHC-P
Clonality: Monoclonal
Clone number: SR45-05
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: 1ug/ul
Purification: Protein A affinity purified.
Molecular weight: Predicted band size: 23 kDa
Isotype: IgG
Immunogen: Synthetic peptide within Human Rab9 aa 31-80 / 201.
Positive control: HepG2 cell lysate, K562 cell lysate, Hela, HepG2, human breast tissue.
Subcellular location: Cell membrane, Endoplasmic reticulum membrane, Golgi apparatus membrane.
Recommended Dilutions:
  WB
  IF-Cell
  IF-Tissue
  IHC-P

1:500
1:50
1:50
1:50
Uniprot #: SwissProt: P51151 Human | Q9R0M6 Mouse | Q99P75 Rat
Alternative names: 2410064E05Rik AI195561 DmRab9 Rab 9 RAB 9A RAB9 member RAS oncogene family RAB9A RAB9A member RAS oncogene family RAB9A_HUMAN RAS ASSOCIATED PROTEIN RAB9 Ras related protein Rab 9A Ras-related protein Rab-9A Sid6061p Sid99
Images
ET1602-29_1.jpg Fig1: Western blot analysis of Rab9 on different lysates with Rabbit anti-Rab9 antibody (ET1602-29) at 1/500 dilution.

Lane 1: HepG2 cell lysate
Lane 2: K562 cell lysate

Lysates/proteins at 10 µg/Lane.

Predicted band size: 23 kDa
Observed band size: 23 kDa

Exposure time: 2 minutes;

15% SDS-PAGE gel.

Proteins were transferred to a PVDF membrane and blocked with 5% NFDM/TBST for 1 hour at room temperature. The primary antibody (ET1602-29) at 1/500 dilution was used in 5% NFDM/TBST at room temperature for 2 hours. Goat Anti-Rabbit IgG - HRP Secondary Antibody (HA1001) at 1:300,000 dilution was used for 1 hour at room temperature.
ET1602-29_2.jpg Fig2: ICC staining of Rab9 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 (ET1602-29, 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).
ET1602-29_3.jpg Fig3: ICC staining of Rab9 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 (ET1602-29, 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).
ET1602-29_4.jpg Fig4: Immunohistochemical analysis of paraffin-embedded human breast tissue using anti-Rab9 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 (ET1602-29, 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”.