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Recombinant Mouse RELT/TNFRSF19L Fc Chimera Protein, CF  50 UG图1

Recombinant Mouse RELT/TNFRSF19L Fc Chimera Protein, CF 50 UG

2024-11-24 18:48IP属地 广东省东莞市 电信00留言

7465-RT

 

Formulation Lyophilized from a 0.2 μm filtered solution in PBS.


Reconstitution Reconstitute at 500 μg/mL in PBS.



Shipping The product is shipped at ambient temperature. Upon receipt, store it immediately at the temperature recommended below.


Stability & Storage:       Use a manual defrost freezer and avoid repeated freeze-thaw cycles.      

  • 12 months from date of receipt, -20 to -70 °C as supplied.

  • 1 month, 2 to 8 °C under sterile conditions after reconstitution.

  • 3 months, -20 to -70 °C under sterile conditions after reconstitution.


Background: RELT/TNFRSF19L

RELT (Receptor Expressed in Lymphoid Tissues) is a 46 kDa (predicted) type I transmembrane glycoprotein belonging to the tumor necrosis factor receptor superfamily and designated TNFRSF19‑like (TNFRSF19L) (1, 2). It is primarily expressed in hematopoietic tissues and peripheral blood leukocytes (2, 3). Mouse RELT cDNA encodes 436 amino acids (aa), including a 31 aa signal peptide, a 138 aa extracellular domain (ECD) containing a TNF receptor cysteine‑rich domain and a potential N‑linked glycosylation site, a 21 aa transmembrane domain, and a 246 aa cytoplasmic region that lacks a death domain (2). Within the ECD, mouse RELT shares 78%, 89%, 70%, 70% and 67% aa sequence homology with human, rat, canine, porcine and bovine RELT, respectively. Among TNFRSF members, the RELT extracellular domain is most closely related to that of TROY/TNFRSF19 and OX40 (2). Neither human nor mouse RELT bind any of the ~19 TNF superfamily ligands that have been tested (1). Two related transmembrane proteins, RELL1 and RELL2, have been identified in both human and mouse (3). RELL1 and 2 are coexpressed with and can interact with RELT, and are thought to modulate its signaling (3‑5). Intracellularly, RELT has been shown to bind the adaptor protein TRAF‑1 and activate the NF‑ kappa B pathway, the phospholipid scramblase PLSCR1, and the oxidative stress responsive protein OSR1 (2‑5). Another investigator notes association and signaling through SPAK, but not TRAF or NF kappa B (6). When overexpressed in HEK‑293 cells, RELT induces p38 and JNK signaling and activates apoptosis (4‑6).

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