Cripto1 Recombinant Rabbit Monoclonal Antibody [JE33-31]
cat.: HA721587
Product Type: Recombinant Rabbit monoclonal IgG, primary antibodies
Species reactivity: Human
Applications: WB, IF-Cell, FC
Clonality: Monoclonal
Clone number: JE33-31
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: 21 kDa
Isotype: IgG
Immunogen: Synthetic peptide.
Positive control: NCCIT cell lysates, NCCIT.
Subcellular location: Cell membrane, Secreted.
Recommended Dilutions:
  WB
  IF-Cell
  FC

1:1,000
1:100
1:50-1:1,000
Uniprot #: SwissProt: P13385 Human
Alternative names: CR CRGF Cripto 1 Cripto 1 growth factor cripto Cripto-1 growth factor Cripto1 growth factor Epidermal growth factor like cripto protein CR1 Epidermal growth factor-like cripto protein CR1 TDGF 1 TDGF1 TDGF1_HUMAN Teratocarcinoma derived growth factor 1 Teratocarcinoma-derived growth factor 1
Images
HA721587_1.jpg Fig1: Western blot analysis of Cripto1 on NCCIT cell lysates with Rabbit anti-Cripto1 antibody (HA721587) at 1/1,000 dilution.

Lysates/proteins at 20 µg/Lane.

Predicted band size: 21 kDa
Observed band size: 21 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 (HA721587) 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.
HA721587_2.jpg Fig2: Immunocytochemistry analysis of NCCIT cells labeling Cripto1 with Rabbit anti-Cripto1 antibody (HA721587) 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-Cripto1 antibody (HA721587) 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.
HA721587_3.jpg Fig3: Flow cytometric analysis of NCCIT cells labeling Cripto1.

Cells were fixed and permeabilized. Then stained with the primary antibody (HA721587, 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”.