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Human PDIA3 / ERp57 Recombinant (His) Protein LS-G13918


Wt. Vol. Conc. Price
10 µg - - $265
50 µg - - $365
100 µg - - $475
Inquire for larger quantities
LSBio (Direct) LSBio (Direct)

Most Popular PDIA3 / ERp57 Proteins

Human PDIA3 / ERp57 Recombinant (His) Protein - LS-G687
E. coli Expression System
Unpurified / Lyophilized
Sodium Dodecyl Sulfate - Polyacrylamide Gel Electrophoresis Image
Human PDIA3 / ERp57 Recombinant (His) Protein - LS-G17693
E. coli Expression System
Unpurified / Lyophilized
Human PDIA3 / ERp57 Recombinant (6His,C-terminus) Protein - LS-G39432
Human Human Cells
Unpurified / Lyophilized

100% Guaranteed 100% Guaranteed
Recombinant Protein
PDIA3 / ERp57
30.8 kDa
aa 162-416
E. coli
E. coli
Greater than 95%
Lyophilized from PBS, pH 7.4, 5% trehalose, 0.01% sarcosyl
Reconstitute in sterile PBS, pH 7.2-7.4.
Store at +4°C for up to 1 month, or aliquot and store at -80°C for up to 12 months. Avoid repeat freeze-thaw cycles.
For research use only.

About PDIA3 / ERp57

P30101 NM_005313 NP_005304.3

PDIA3 Protein, 58 kDa microsomal protein Protein, ER protein 57 Protein, ERp60 Protein, ERp61 Protein, Disulfide isomerase ER-60 Protein, Endoplasmic reticulum P58 Protein, GRP58 Protein, HsT17083 Protein, p58 Protein, Phospholipase C-alpha Protein, PI-PLC Protein, ER protein 60 Protein, ER60 Protein, ERp57 Protein, GRP57 Protein, Protein disulfide-isomerase A3 Protein

PDIA3 / ERp57 encodes a protein of the endoplasmic reticulum that interacts with lectin chaperones calreticulin and calnexin to modulate folding of newly synthesized glycoproteins. The protein was once thought to be a phospholipase; however, it has been demonstrated that the protein actually has protein disulfide isomerase activity. It is thought that complexes of lectins and this protein mediate protein folding by promoting formation of disulfide bonds in their glycoprotein substrates.

Sodium Dodecyl Sulfate - Polyacrylamide Gel Electrophoresis

Sodium Dodecyl Sulfate - Polyacrylamide Gel Electrophoresis

Requested From: United States
Date Requested: 10/24/2016

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