Calreticulin Mouse Monoclonal Antibody [7B1]
cat.: EM1701-60
Product Type: Mouse monoclonal IgG1, primary antibodies
Species reactivity: Human
Applications: WB, IHC-P, IF-Cell, FC
Clonality: Monoclonal
Clone number: 7B1
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: Protein G affinity purified.
Molecular weight: Predicted band size: 48 kDa
Isotype: IgG1
Immunogen: Recombinant full length protein corresponding to Human Calretinin aa 1 to the C-terminus.
Positive control: HepG2 cell lysate, HeLa cell lysate, HL-60 cell lysate, HepG2, human prostate cancer tissue, Jurkat.
Subcellular location: Endoplasmic reticulum. Secreted. Cytosol.
Recommended Dilutions:
  WB
  IF-Cell
  IHC-P
  FC

1:5,000
1:50-1:200
1:50-1:200
1:50-1:100
Uniprot #: SwissProt: P27797 Human
Alternative names: Autoantigen RO CALR CALR protein CALR_HUMAN Calregulin Calreticulin cC1qR CRP55 CRT CRTC Endoplasmic reticulum resident protein 60 Epididymis secretory sperm binding protein Li 99n ERp60 FLJ26680 grp60 HACBP HEL S 99n RO Sicca syndrome antigen A (autoantigen Ro; calreticulin) Sicca syndrome antigen A SSA
Images
EM1701-60_1.jpg Fig1: Western blot analysis of Calreticulin on different lysates with Mouse anti-Calreticulin antibody (EM1701-60) at 1/5,000 dilution.

Lane 1: HepG2 cell lysate (20 µg/Lane)
Lane 2: HeLa cell lysate (20 µg/Lane)
Lane 3: HL-60 cell lysate (20 µg/Lane)

Predicted band size: 48 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 (EM1701-60) at 1/5,000 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.
EM1701-60_2.jpg Fig2: Western blot analysis of Calreticulin on different lysates with Mouse anti-Calreticulin antibody (EM1701-60) at 1/500 dilution.

Lane 1: Hela-si NT cell lysate (10 µg/Lane)
Lane 2: Hela-si Calreticulin cell lysate (10 µg/Lane)

Predicted band size: 48 kDa
Observed band size: 55 kDa

Exposure time: 5 seconds;

4-20% SDS-PAGE gel.

EM1701-60 was shown to specifically react with Calreticulin in Hela-si NT cells. Weakened band was observed when Hela-si Calreticulin sample was tested. Hela-si NT and Hela-si Calreticulin samples were subjected to SDS-PAGE. Proteins were transferred to a PVDF membrane and blocked with 5% NFDM in TBST for 1 hour at room temperature. The primary antibody (EM1701-60, 1/500) and Loading control antibody (Rabbit anti-GAPDH, ET1601-4, 1/10,000) were used in 5% BSA at room temperature for 2 hours. Goat Anti-mouse IgG-HRP Secondary Antibody (HA1006) at 1:150,000 dilution was used for 1 hour at room temperature.
EM1701-60_3.jpg Fig3: ICC staining Calreticulin (green) in HepG2 cells. The nuclear counter stain is DAPI (blue). Cells were fixed in paraformaldehyde, permeabilised with 0.25% Triton X100/PBS.
EM1701-60_4.jpg Fig4: Immunohistochemical analysis of paraffin-embedded human prostate cancer tissue using anti-Calreticulin antibody. Counter stained with hematoxylin.
EM1701-60_5.jpg Fig5: Flow cytometric analysis of Jurkat cells with Calreticulin antibody at 1/100 dilution (red) compared with an unlabelled control (cells without incubation with primary antibody; black). 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”.