AdipoGen Life Sciences

Calreticulin (human) (rec.) (His)

CHF 230.00
In stock
AG-40A-0132-C01010 µgCHF 230.00
AG-40A-0132-C05050 µgCHF 590.00
More Information
Product Details
Synonyms CRP55; Calregulin; Endoplasmic Reticulum Resident Protein 60; ERp60; grp60
Product Type Protein
Properties
Source/Host E. coli
Sequence

Human calreticulin (aa18-417) is fused at the C-terminus to a His-tag.

Crossreactivity Human
MW ~55kDa (SDS-PAGE)
Purity ≥90% (SDS-PAGE)
Purity Detail Purified using Ni-NTA column and FPLC.
Endotoxin Content <1EU/μg purified protein (LAL test; Lonza).
Concentration 0.2mg/ml
Formulation Liquid. 0.2μm-filtered solution in 55mM TRIS-HCl, pH 8.2, containing 150mM NaCl.
Other Product Data

UniProt link P27797: Calreticulin (human)

Shipping and Handling
Shipping BLUE ICE
Short Term Storage +4°C
Long Term Storage -20°C
Handling Advice After opening, prepare aliquots and store at -20°C.
Avoid freeze/thaw cycles.
For maximum product recovery after thawing, centrifuge the vial before opening the cap.
Use/Stability Stable for at least 6 months after receipt when stored at -20°C.
Working aliquots are stable for up to 3 months when stored at -20°C.
Documents
MSDS Download PDF
Product Specification Sheet
Datasheet Download PDF
Description

Calreticulin is involved in regulation of intracellular Ca2+ homoeostasis and ER Ca2+ capacity. It constitutes together with calnexin and ERp57 the 'calreticulin/calnexin cycle' that is responsible for folding and quality control of newly synthesized glycoproteins. Calreticulin has been implicated to play a role in many biological systems, including functions inside and outside the ER, indicating that the protein is a multi-process molecule. Calreticulin was shown to enhance the merger of macrophages and tumor cells, increasing phagocytosis. Recently, calreticulin has been identified as an endogenous ligand of the NK cell receptor NKp46. NKp46 recognizes externalized calreticulin (ecto-CRT), which translocates from the endoplasmic reticulum (ER) to the cell membrane during ER stress. ER stress and ecto-CRT are hallmarks of chemotherapy-induced immunogenic cell death, favivirus infection and senescence. NKp46-mediated killing is inhibited by knockout or knockdown of CALR, the gene encoding CRT, or CRT antibodies, and is enhanced by ectopic expression of glycosylphosphatidylinositol-anchored CRT. NKp46 recognition of ecto-CRT as a danger-associated molecular pattern eliminates ER-stressed cells.

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