FAT tumor suppressor homolog 4 Rabbit Polyclonal Antibody
cat.: 0905-1
Product Type: Rabbit polyclonal IgG, primary antibodies
Species reactivity: Human
Applications: WB, IF-Cell
Clonality: Polyclonal
Form: Liquid
Storage condition: Store at +4℃ after thawing. Aliquot store at -20℃ or -80℃. Avoid repeated freeze / thaw cycles.
Storage buffer: 1*PBS (pH7.4), 0.2% BSA, 40% Glycerol. Preservative: 0.05% Sodium Azide.
Concentration: 1ug/ul
Purification: Immunogen affinity purified.
Molecular weight: Predicted band size: 543 kDa
Isotype: IgG
Immunogen: Synthetic peptide within Human FAT tumor suppressor homolog 4 aa 2,264-2,313 / 4,981.
Positive control: HepG2, Lovo.
Subcellular location: Membrane
Recommended Dilutions:
  WB
  IF-Cell

1:500~1:1,000
1:50-1:100
Uniprot #: SwissProt: Q6V0I7 Human
Alternative names: Cadherin family member 14 Cadherin related family member 11 CDHF14 CDHR11 FAT atypical cadherin 4 FAT J FAT tumor suppressor homolog 4 Fat-like cadherin protein FAT-J FAT4 FAT4_HUMAN FATJ hFat4 HKLLS2 Nbla00548 Protocadherin Fat 4 Putative protein product of Nbla00548 VMLDS2
Images
0905-1_1.jpg Fig1: Western blot analysis on recombinant FAT4 using anti-FAT4 polyclonal antibody.
0905-1_2.png Fig2: Immunocytochemistry analysis of HepG2 cells labeling FAT tumor suppressor homolog 4 with Rabbit anti-FAT tumor suppressor homolog 4 antibody (0905-1) at 1/200 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-FAT tumor suppressor homolog 4 antibody (0905-1) at 1/200 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. PBS instead of the primary antibody was used as the secondary antibody only control. Nuclear DNA was labelled in blue with DAPI.
0905-1_3.png Fig3: Immunocytochemistry analysis of Lovo cells labeling FAT tumor suppressor homolog 4 with Rabbit anti-FAT tumor suppressor homolog 4 antibody (0905-1) 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-FAT tumor suppressor homolog 4 antibody (0905-1) 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. PBS instead of the primary antibody was used as the secondary antibody only control. Nuclear DNA was labelled in blue with DAPI.
Note: All products are “FOR RESEARCH USE ONLY AND ARE NOT INTENDED FOR DIAGNOSTIC OR THERAPEUTIC USE”.