eIF3A Recombinant Rabbit Monoclonal Antibody [JE58-60]
cat.: HA721375
Product Type: Recombinant Rabbit monoclonal IgG, primary antibodies
Species reactivity: Human, Mouse, Rat
Applications: WB, IHC-P, IF-Cell
Clonality: Monoclonal
Clone number: JE58-60
Form: Liquid
Storage condition: Store at +4℃ after thawing. Aliquot store at -20℃. Avoid repeated freeze / thaw cycles.
Storage buffer: 1*TBS (pH7.4), 0.05% BSA, 40% Glycerol. Preservative: 0.05% Sodium Azide.
Concentration: 1ug/ul
Purification: Protein A affinity purified.
Molecular weight: Predicted band size: 167 kDa
Isotype: IgG
Immunogen: Synthetic peptide within Human eIF3A aa 275-324 / 1,382.
Positive control: 293T cell lysate, A431 cell lysate, Jurkat cell lysate, Raji cell lysate, RAW264.7 cell lysate, NIH/3T3 cell lysate, L6 cell lysate, PC-12 cell lysate, mouse brain tissue, rat brain tissue, Hela.
Subcellular location: Cytoplasm.
Recommended Dilutions:
  WB
  IHC-P
  IF-Cell

1:1,000
1:1,000
1:100
Uniprot #: SwissProt: Q14152 Human | P23116 Mouse | Q1JU68 Rat
Alternative names: centrosomin homolog cytoplasmic protein p167 eIF 3 theta eIF-3-theta EIF3 eIF3 p167 eIF3 p170 eIF3 p180 EIF3 p180 subunit eIF3 p185 eIF3 theta eIF3a EIF3A_HUMAN EIF3S10 eukaryotic translation initiation factor 3 subunit 10 (theta 150 170kD) eukaryotic translation initiation factor 3 subunit 10 (theta 170kD) eukaryotic translation initiation factor 3 subunit 10 170kDa Eukaryotic translation initiation factor 3 subunit 10 eukaryotic translation initiation factor 3 subunit 10 theta 150 170kDa Eukaryotic translation initiation factor 3 subunit A OTTHUMP00000020589 P167 p180 p185 TIF32
Images
HA721375_1.jpg Fig1: Western blot analysis of eIF3A on different lysates with Rabbit anti-eIF3A antibody (HA721375) at 1/1,000 dilution.

Lane 1: 293T cell lysate
Lane 2: A431 cell lysate
Lane 3: Jurkat cell lysate
Lane 4: Raji cell lysate
Lane 5: RAW264.7 cell lysate
Lane 6: NIH/3T3 cell lysate
Lane 7: L6 cell lysate
Lane 8: PC-12 cell lysate

Lysates/proteins at 15 µg/Lane.

Predicted band size: 167 kDa
Observed band size: 167 kDa

Exposure time: 7seconds;

4-20% 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 (HA721375) at 1/1,000 dilution was used in 5% NFDM/TBST at room temperature for 2 hours. Goat Anti-Rabbit IgG - HRP Secondary Antibody (HA1001) at 1:100,000 dilution was used for 1 hour at room temperature.
HA721375_2.jpg Fig2: Immunohistochemical analysis of paraffin-embedded mouse brain tissue with Rabbit anti-eIF3A antibody (HA721375) at 1/1,000 dilution.

The section was pre-treated using heat mediated antigen retrieval with Tris-EDTA buffer (pH 9.0) for 20 minutes. The tissues were blocked in 1% BSA for 20 minutes at room temperature, washed with ddH2O and PBS, and then probed with the primary antibody (HA721375) at 1/1,000 dilution for 1 hour 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.
HA721375_3.jpg Fig3: Immunohistochemical analysis of paraffin-embedded rat brain tissue with Rabbit anti-eIF3A antibody (HA721375) at 1/1,000 dilution.

The section was pre-treated using heat mediated antigen retrieval with Tris-EDTA buffer (pH 9.0) for 20 minutes. The tissues were blocked in 1% BSA for 20 minutes at room temperature, washed with ddH2O and PBS, and then probed with the primary antibody (HA721375) at 1/1,000 dilution for 1 hour 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.
HA721375_4.jpg Fig4: Immunocytochemistry analysis of Hela cells labeling eIF3A with Rabbit anti-eIF3A antibody (HA721375) at 1/100 dilution.

Cells were fixed in 4% paraformaldehyde for 10 minutes at 37 ℃, permeabilized with 0.05% Triton X-100 in PBS for 20 minutes, and then blocked with 2% negative goat serum for 30 minutes at room temperature. Cells were then incubated with Rabbit anti-eIF3A antibody (HA721375) at 1/100 dilution in 2% negative goat serum overnight at 4 ℃. Goat Anti-Rabbit IgG H&L (iFluor™ 488, HA1121) was used as the secondary antibody at 1/1,000 dilution. Nuclear DNA was labelled in blue with DAPI.

Beta tubulin (M1305-2, red) was stained at 1/200 dilution overnight at +4℃. Goat Anti-Mouse IgG H&L (iFluor™ 594, HA1126) was used as the secondary antibody at 1/1,000 dilution.
HA721375_5.jpg Fig5: Immunocytochemistry analysis of A431 cells labeling eIF3A with Rabbit anti-eIF3A antibody (HA721375) at 1/100 dilution.

Cells were fixed in 4% paraformaldehyde for 10 minutes at 37 ℃, permeabilized with 0.05% Triton X-100 in PBS for 20 minutes, and then blocked with 2% negative goat serum for 30 minutes at room temperature. Cells were then incubated with Rabbit anti-eIF3A antibody (HA721375) at 1/100 dilution in 2% negative goat serum overnight at 4 ℃. Goat Anti-Rabbit IgG H&L (iFluor™ 488, HA1121) was used as the secondary antibody at 1/1,000 dilution. Nuclear DNA was labelled in blue with DAPI.

Beta tubulin (M1305-2, red) was stained at 1/200 dilution overnight at +4℃. Goat Anti-Mouse IgG H&L (iFluor™ 594, HA1126) was used as the secondary antibody at 1/1,000 dilution.
Note: All products are “FOR RESEARCH USE ONLY AND ARE NOT INTENDED FOR DIAGNOSTIC OR THERAPEUTIC USE”.