CYFIP1 Recombinant Rabbit Monoclonal Antibody [JE64-11]
cat.: HA721095
Product Type: Recombinant Rabbit monoclonal IgG, primary antibodies
Species reactivity: Human, Mouse, Rat
Applications: WB, IHC-P
Clonality: Monoclonal
Clone number: JE64-11
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: 145 kDa
Isotype: IgG
Immunogen: Synthetic peptide within human CYFIP1 aa 51-100/1,253.
Positive control: SW480 cell lysate, RAW264.7 cell lysate, rat lung tissue lysate, NIH/3T3 cell lysate, rat lung tissue lysates, rat esophagus tissue, rat stomach tissue.
Subcellular location: Cytoplasm, perinuclear region, lamellipodium, ruffle, synaptosome.
Recommended Dilutions:
  WB
  IHC-P

1:500
1:100-1:400
Uniprot #: SwissProt: Q7L576 Human | Q7TMB8 Mouse
Entrez Gene: 308666 Rat
Alternative names: CY CYFIP 1 CYFIP1 CYFP1_HUMAN Cytoplasmic FMR1 interacting protein 1 Cytoplasmic FMR1-interacting protein 1 FLJ45151 KIAA0068 p140sra 1 p140sra-1 P140SRA1 Selective hybridizing clone SHYC Specifically Rac1 associated protein 1 Specifically Rac1-associated protein 1 SRA 1 Sra-1 SRA1
Images
HA721095_1.jpg Fig1: Western blot analysis of CYFIP1 on different lysates with Rabbit anti-CYFIP1 antibody (HA721095) at 1/500 dilution.

Lane 1: SW480 cell lysate
Lane 2: RAW264.7 cell lysate

Lysates/proteins at 10 µg/Lane.

Predicted band size: 145 kDa
Observed band size: 130 kDa

Exposure time: 2 minutes;

6% 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 (HA721095) 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.
HA721095_2.jpg Fig2: Western blot analysis of CYFIP1 on different lysates with Rabbit anti-CYFIP1 antibody (HA721095) at 1/500 dilution.

Lane 1: Rat lung tissue lysate (20 µg/Lane)
Lane 2: NIH/3T3 cell lysate (10 µg/Lane)

Lysates/proteins at 10 µg/Lane.

Predicted band size: 145 kDa
Observed band size: 130 kDa

Exposure time: 2 minutes;

6% 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 (HA721095) 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.
HA721095_3.jpg Fig3: Western blot analysis of CYFIP1 on rat lung tissue lysates with Rabbit anti-CYFIP1 antibody (HA721095) at 1/500 dilution.

Lysates/proteins at 20 µg/Lane.

Predicted band size: 145 kDa
Observed band size: 130 kDa

Exposure time: 30 minutes;

6% 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 (HA721095) 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.
HA721095_4.jpg Fig4: Immunohistochemical analysis of paraffin-embedded rat esophagus tissue with Rabbit anti-CYFIP1 antibody (HA721095) at 1/100 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 (HA721095) at 1/100 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.
HA721095_5.jpg Fig5: Immunohistochemical analysis of paraffin-embedded rat stomach tissue with Rabbit anti-CYFIP1 antibody (HA721095) at 1/400 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 (HA721095) at 1/400 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.
Note: All products are “FOR RESEARCH USE ONLY AND ARE NOT INTENDED FOR DIAGNOSTIC OR THERAPEUTIC USE”.