WNT8A Recombinant Rabbit Monoclonal Antibody [PSH0-39]
cat.: HA721341
Product Type: Recombinant Rabbit monoclonal IgG, primary antibodies
Species reactivity: Human, Mouse, Rat
Applications: WB, IF-Cell, FC
Clonality: Monoclonal
Clone number: PSH0-39
Form: Liquid
Storage condition: Store at +4℃ after thawing. Aliquot store at -20℃. Avoid repeated freeze / thaw cycles.
Storage buffer: PBS (pH7.4), 0.1% BSA, 40% Glycerol. Preservative: 0.05% Sodium Azide.
Concentration: 1ug/ul
Purification: Protein A affinity purified.
Molecular weight: Predicted band size: 38.8 kDa
Isotype: IgG
Immunogen: Recombinant protein within human WNT8A aa 100-300 / 351.
Positive control: HeLa cell lysate, HepG2 cell lysate, SW480 cell lysate, Jurkat cell lysate, Raji cell lysate, NIH/3T3 cell lysate, mouse brain tissue lysate, mouse embryo tissue lysate, rat brain tissue lysate, NIH/3T3, HeLa.
Subcellular location: Secreted, extracellular space, extracellular matrix.
Recommended Dilutions:
  WB
  IF-Cell
  FC

1:1,000
1:50
1:500-1:1,000
Uniprot #: SwissProt: Q9H1J5 Human | Q64527 Mouse
Entrez Gene: 291678 Rat
Alternative names: Protein Wnt-8a Protein Wnt-8d wingless type MMTV integration site family, member 8A WNT 8A Wnt 8d wnt8a WNT8A_HUMAN WNT8D
Images
HA721341_1.jpg Fig1: Western blot analysis of WNT8A on different lysates with Rabbit anti-WNT8A antibody (HA721341) at 1/1,000 dilution.

Lane 1: HeLa cell lysate (30 µg/Lane)
Lane 2: HepG2 cell lysate (30 µg/Lane)
Lane 3: SW480 cell lysate (30 µg/Lane)
Lane 4: Jurkat cell lysate (30 µg/Lane)
Lane 5: Raji cell lysate (30 µg/Lane)
Lane 6: NIH/3T3 cell lysate (30 µg/Lane)
Lane 7: Mouse brain tissue lysate (40 µg/Lane)
Lane 8: Mouse embryo tissue lysate (40 µg/Lane)
Lane 9: Rat brain tissue lysate (40 µg/Lane)

Predicted band size: 38.8 kDa
Observed band size: 55 kDa

Exposure time: 1 minute;

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 (HA721341) 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 1:200,000 dilution was used for 1 hour at room temperature.
HA721341_2.jpg Fig2: Immunocytochemistry analysis of NIH/3T3 cells labeling WNT8A with Rabbit anti-WNT8A antibody (HA721341) at 1/50 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-WNT8A antibody (HA721341) at 1/50 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 1/100 dilution overnight at +4℃. Goat Anti-Mouse IgG H&L (iFluor™ 594, HA1126) was used as the secondary antibody at 1/1,000 dilution.
HA721341_3.jpg Fig3: Flow cytometric analysis of HeLa cells labeling WNT8A.

Cells were fixed and permeabilized. Then stained with the primary antibody (HA721341, 1ug/ml) (red) compared with Rabbit IgG Isotype Control (green). After incubation of the primary antibody at +4℃ for an hour, the cells were stained with a iFluor™ 488 conjugate-Goat anti-Rabbit IgG Secondary antibody (HA1121) at 1/1,000 dilution for 30 minutes at +4℃. Unlabelled sample was used as a control (cells without incubation with primary antibody; black).
HA721341_4.jpg Fig4: Flow cytometric analysis of NIH/3T3 cells labeling WNT8A.

Cells were fixed and permeabilized. Then stained with the primary antibody (HA721341, 1ug/ml) (red) compared with Rabbit IgG Isotype Control (green). After incubation of the primary antibody at +4℃ for an hour, the cells were stained with a iFluor™ 488 conjugate-Goat anti-Rabbit IgG Secondary antibody (HA1121) at 1/1,000 dilution for 30 minutes at +4℃. 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”.