ABS1671

Anti-Calreticulin Antibody, arginylated (Nt-Glu18)

from rabbit, purified by affinity chromatography

• Synonym(s): Calreticulin, Nt-Glu18 arginylated, Calregulin, Nt-Glu18 arginylated, CRP55, Nt-Glu18 arginylated, CRT, Nt-Glu18 arginylated, Endoplasmic reticulum resident protein 60, Nt-Glu18 arginylated, ERp60, Nt-Glu18 arginylated, grp60, Nt-Glu18 arginylated, HACBP
• UNSPSC Code: 12352203
• eCl@ss: 32160702

Properties

• biological source: rabbit
• Quality Level: 100
• antibody form: affinity isolated antibody
• antibody product type: primary antibodies
• clone: polyclonal
• purified by: affinity chromatography
• species reactivity: human
• technique(s): ELISA: suitable; immunocytochemistry: suitable; western blot: suitable
• NCBI accession no.: NP_004334
• UniProt accession no.: P27797
• shipped in: ambient
• target post-translational modification: unmodified
• Gene Information: human ... CALR(811)

Description

General description

Calreticulin (UniProt P27797; also known as Calregulin, CRP55, CRT, Endoplasmic reticulum resident protein 60, ERp60, grp60, HACBP) is encoded by the CALR (also known as CRTC) gene (Gene ID 811) in human. Calreticulin (CRT), BiP (GRP78 or heat shock 70 kDa protein 5), and protein disulphide isomerase (PDI) are ER lumen folding factors that, together with other PTM enzymes, assist the process of newly synthesized proteins before their release from ER. CRT, BiP, and PDI themselves are subject to posttranslational signal peptide removal after their synthesis, exposing E18, E19, and D18 at the newly formed N-terminus, respectively. The N-terminus D and E residues of the mature proteins are permissive to arginine-tRNA-protein transferase 1/ATE1-catalyzed arginylation, forming arginylated mature proteins (R-CRT, R-BiP, R-PDI) with altered cellular localization to allow their participation in non-ER functions. Although only the basal levels of R-CRT and R-PDI, but not R-BiP, are generally detectible in non-stimulated cells, upregulated N-terminal arginylation of all three proteins is observed upon cytosolic dsDNA exposure and proteasomal inhibition, indicating a shared role in innate immune responses to invading microbes. In addition, ER stress induction by thapsigargin treatment synergistically boosts proteasomal inhibition-induced upregulation of cellular levels of R-CRT, R-BiP, and R-PDI, suggesting that ER stress accelerates the supply of ER lumenal CRT, BiP, and DPI for N-terminal arginylation.

Specificity

This rabbit polyclonal antibody specifically detected the immunogen peptide, but not the control peptide without arginylation at the N-terminal Glu18 (Cha-Molstad, H., et al. (2015). Nat. Cell Biol. 17(7):917-929).

Immunogen

Epitope: N-terminus

Linear peptide corresponding to the N-terminal sequence of arginylated mature human Calreticulin.

Application

Detect arginylated mature calreticulin using this rabbit polyclonal Anti-Calreticulin, arginylated (Nt-Glu18), Cat. No. ABS1671, validated for use in ELISA, Immunocytochemistry, and Western Blotting.

Immunocytochemistry Analysis: A 1:100 dilution from a representative lot detected Calreticulin Nt-Glu18 arginylation induction in (18-hr 3 µM MG132 and 200 nM thapsigargin) treated HeLa cells (Courtesy of Yong Tae Kwon, Ph.D. , Seoul National University, Korea).

Western Blotting Analysis: 0.2 µg/mL from a representative lot detected Calreticulin Nt-Glu18 arginylation induction in (18-hr 3 µM MG132 and 200 nM thapsigargin) treated HeLa cells (Courtesy of Yong Tae Kwon, Ph.D. , Seoul National University, Korea).

ELISA Analysis: A representative lot detected the immunogen peptide, but not the control peptide without arginylation at the N-terminal Glu18 (Cha-Molstad, H., et al. (2015). Nat. Cell Biol. 17(7):917-929).

Western Blotting Analysis: A representative lot detected Calreticulin Nt-Glu18 arginylation induction upon arginine-tRNA-protein transferase 1 (ATE1) 1A7A isoform overexpression or transfection of various dsDNAs, including poly(dA:dT), in HeLa cells. Combined proteasome inhibition and ER stress induction by an 18-hr 10 µM MG132 and 100 nM thapsigargin treatment synergized the two drugs′ efficacy toward cellular Calreticulin Nt-Glu18 arginylation induction (Cha-Molstad, H., et al. (2015). Nat. Cell Biol. 17(7):917-929).

Research Category
Signaling

Quality

Evaluated by Western Blotting in HEK293 cell lysate.

Western Blotting Analysis: 1 µg/mL of this antibody detected Calreticulin Nt-Glu18 arginylation induction in 7.5 µg of lysate from (17-hr 3 µM MG132 and 200 nM thapsigargin) treated HEK293 cells.

Target description

~55 kDa observed. 46.6 kDa calculated. Uncharacterized bands may be observed in some lysate(s).

Physical form

Affinity purified.

Purified rabbit polyclonal antibody in buffer containing PBS with 0.05% sodium azide.

Storage and Stability

Stable for 1 year at 2-8°C from date of receipt.

Other Notes

Concentration: Please refer to lot specific datasheet.

Disclaimer

Unless otherwise stated in our catalog or other company documentation accompanying the product(s), our products are intended for research use only and are not to be used for any other purpose, which includes but is not limited to, unauthorized commercial uses, in vitro diagnostic uses, ex vivo or in vivo therapeutic uses or any type of consumption or application to humans or animals.

Safety Information

• Storage Class: 12 - Non Combustible Liquids
• wgk_germany: WGK 2
• flash_point_f: Not applicable
• flash_point_c: Not applicable