Recombinant humaan SSSCA1/ZNRD2-eiwit

SSSCA1 is recognized by a subset of anti-centromere antibodies from patients with scleroderma and/or Sjogren's syndrome. Subcellular localization has not yet been established. Recombinant human SSSCA1 protein, fused to His-tag at N-terminus, was expressed in E. coli.

Sjoegren syndrome/scleroderma autoantigen 1, Zinc ribbon domain containing 2

E.coli

Human

His-Tag

SDS-PAGE, Denatured

0.5 mg/mL (determined by Bradford assay)

> 90% by SDS-PAGE

23.9 kDa (222aa)

Zinc ribbon domain containing 2, SSSCA1, Sjoegren syndrome/scleroderma autoantigen 1, p27, ATGP2396-10 µg, ATGP2396-20 µg, ATGP2396-50 µg, ATGP2396-100 µg, ATGP2396-250 µg, ATGP2396-500 µg, ATGP2396-1 mg, ATGP2396-010, ATGP2396-020, ATGP2396-050, ATGP2396-100, ATGP2396-250, ATGP2396-500, ATGP2396-01M

Ananthanarayanan, V., et al. (2011) Hum. Pathol. 42 (6), 873-881; ; Lango Allen, H., et al. (2010) Nature 467 (7317), 832-838;

Can be stored at 2°C to 8°C for 1 week. For long term storage, aliquot and store at -20C to -80C. Avoid repeated freezing and thawing cycles.

Liquid in. 20 mM Tris-HCl buffer (pH 8.0) containing 10% glycerol 0.4M urea

Immunology

NP_006387

O60232

Human

MALNGAE VDDFSWEPPT EAETKVLQAR RERQDRISRL MGDYLLRGYR MLGETCADCG TILLQDKQRK IYCVACQELD SDVDKDNPAL NAQAALSQAR EHQLASASEL PLGSRPAPQP PVPRPEHCEG AAAGLKAAQG PPAPAVPPNT DVMACTQTAL LQKLTWASAE LGSSTSLETS IQLCGLIRAC AEALRSLQQL QH