ASS1 Mouse Monoclonal Antibody [11F1]
cat.: EM1701-87
Product Type: Mouse monoclonal IgG2b, primary antibodies
Species reactivity: Human, Mouse
Applications: WB, IHC-P, IF-Cell, FC
Clonality: Monoclonal
Clone number: 11F1
Form: Liquid
Storage condition: Store at +4℃ after thawing. Aliquot store at -20℃. Avoid repeated freeze / thaw cycles.
Storage buffer: 1*PBS (pH7.4), 0.2% BSA, 50% Glycerol. Preservative: 0.05% Sodium Azide.
Concentration: 2ug/ul
Purification: Immunogen affinity purified.
Molecular weight: Predicted band size: 47 kDa
Isotype: IgG2b
Immunogen: Recombinant protein within Human ASS1 aa 1-412 / 412.
Positive control: HepG2, MCF-7, SiHa, human colon cancer tissue, mouse testis tissue.
Subcellular location: Cytosol.
Recommended Dilutions:
  WB
  IF-Cell
  IHC-P
  FC

1:500-1:5,000
1:50-1:200
1:50-1:200
1:50-1:100
Uniprot #: SwissProt: P00966 Human | P16460 Mouse
Alternative names: Argininosuccinate synthase 1 Argininosuccinate synthase Argininosuccinate synthetase 1 ASS Ass-1 ass1 ASSA ASSY_HUMAN Citrulline aspartate ligase Citrulline--aspartate ligase CTLN1
Images
EM1701-87_1.jpg Fig1: Western blot analysis of ASS1 on different lysates with Mouse anti-ASS1 antibody (EM1701-87) at 1/5,000 dilution.

Lane 1: HepG2 cell lysate
Lane 2: SiHa cell lysate

Lysates/proteins at 10 µg/Lane.

Predicted band size: 47 kDa
Observed band size: 47 kDa

Exposure time: 30 seconds;

10% 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 (EM1701-87) at 1/5,000 dilution was used in 5% NFDM/TBST at room temperature for 2 hours. Goat Anti-Mouse IgG - HRP Secondary Antibody (HA1006) at 1:100,000 dilution was used for 1 hour at room temperature.
EM1701-87_2.jpg Fig2: Western blot analysis of ASS1 on different lysates with Mouse anti-ASS1 antibody (EM1701-87) at 1/2,000 dilution.

Lane 1: A549-WT cell lysate
Lane 2: A549-KD ASS1 cell lysate

Lysates/proteins at 10 µg/Lane.

Predicted band size: 47 kDa
Observed band size: 45 kDa

Exposure time: 40 seconds; ECL: K1802;

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 (EM1701-87) at 1/2,000 dilution was used in 5% NFDM/TBST at 4℃ overnight. Goat Anti-Mouse IgG - HRP Secondary Antibody (HA1006) at 1/50,000 dilution was used for 1 hour at room temperature.
EM1701-87_3.jpg Fig3: ICC staining ASS1 (green) in MCF-7 cells. The nuclear counter stain is DAPI (blue). Cells were fixed in paraformaldehyde, permeabilised with 0.25% Triton X100/PBS.
EM1701-87_4.jpg Fig4: ICC staining ASS1 (green) in SiHa cells. The nuclear counter stain is DAPI (blue). Cells were fixed in paraformaldehyde, permeabilised with 0.25% Triton X100/PBS.
EM1701-87_5.jpg Fig5: ICC staining ASS1 (green) in HepG2 cells. The nuclear counter stain is DAPI (blue). Cells were fixed in paraformaldehyde, permeabilised with 0.25% Triton X100/PBS.
EM1701-87_6.jpg Fig6: Immunohistochemical analysis of paraffin-embedded human colon cancer tissue using anti-ASS1 antibody. Counter stained with hematoxylin.
EM1701-87_7.jpg Fig7: Immunohistochemical analysis of paraffin-embedded mouse testis tissue using anti-ASS1 antibody. Counter stained with hematoxylin.
EM1701-87_8.jpg Fig8: Flow cytometric analysis of HepG2 cells with ASS1 antibody at 1/100 dilution (purple) compared with an unlabelled control (cells without incubation with primary antibody; yellow). Alexa Fluor 488-conjugated goat anti-mouse IgG was used as the secondary antibody.
Note: All products are “FOR RESEARCH USE ONLY AND ARE NOT INTENDED FOR DIAGNOSTIC OR THERAPEUTIC USE”.