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Recombinant Human CD300b/LMIR5 Fc Chimera Protein, CF

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When Recombinant Human CD300b/LMIR5 Fc Chimera(Catalog # 1522-LM) is immobilized at 2 µg/mL (100 µL/well), Recombinant Human LMIR2/CD300C Fc Chimera (Catalog # 3256-LM) binds with an ED50 of 1.5‑9 μg/mL.
2 μg/lane of Recombinant Human CD300b/LMIR5 Fc Chimera (Catalog # 1522-LM) was resolved with SDS-PAGE underreducing (R) and non-reducing (NR) conditions and visualized by Coomassie® Bluestaining, showing bands at ...read more

Product Details

Summary
Reactivity HuSpecies Glossary
Applications Bioactivity
Format
Carrier-Free

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Recombinant Human CD300b/LMIR5 Fc Chimera Protein, CF Summary

Details of Functionality
Measured by its binding ability in a functional ELISA. When Recombinant Human CD300b/LMIR5 Fc Chimera is immobilized at 2 µg/mL, 100 µL/well, Recombinant Human LMIR2/CD300C Fc Chimera (Catalog # 3256-LM) binds with an ED50 of 1.5-9 μg/mL.
Source
Mouse myeloma cell line, NS0-derived human CD300b/LMIR5 protein
Human CD300b
(Ile55-His187)
Accession # AAH28091
IEGRMD Human IgG1
(Pro100-Lys330)
N-terminusC-terminus
Accession #
N-terminal Sequence
Ile55
Structure / Form
Disulfide-linked homodimer
Protein/Peptide Type
Recombinant Proteins
Purity
>95%, by SDS-PAGE visualized with Silver Staining and quantitative densitometry by Coomassie® Blue Staining.
Endotoxin Note
<0.10 EU per 1 μg of the protein by the LAL method.

Applications/Dilutions

Dilutions
  • Bioactivity
Theoretical MW
42 kDa.
Disclaimer note: The observed molecular weight of the protein may vary from the listed predicted molecular weight due to post translational modifications, post translation cleavages, relative charges, and other experimental factors.
SDS-PAGE
46-59 kDa, reducing conditions

Packaging, Storage & Formulations

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.
Buffer
Lyophilized from a 0.2 μm filtered solution in PBS.
Purity
>95%, by SDS-PAGE visualized with Silver Staining and quantitative densitometry by Coomassie® Blue Staining.
Reconstitution Instructions
Reconstitute at 200 μg/mL in PBS.

Notes

This product is produced by and ships from R&D Systems, Inc., a Bio-Techne brand.

Alternate Names for Recombinant Human CD300b/LMIR5 Fc Chimera Protein, CF

  • CD300 antigen like family member B
  • CD300 antigen-like family member B
  • CD300 molecule-like family member b
  • CD300b antigen
  • CD300b
  • CD300LB
  • CLM7
  • CLM-7
  • CLM7IREM3CD300 molecule like family member b
  • CMRF35A2
  • CMRF35-A2
  • CMRF35-like molecule 7
  • EC 1.13.11.6
  • EC 6.3.4.3
  • Gm253
  • Immune receptor expressed on myeloid cells 3
  • IREM-3
  • Leukocyte mono-Ig-like receptor 5
  • LMIR5
  • TREM-5
  • TREM5CD300b
  • Triggering receptor expressed on myeloid cells 5

Background

LMIR5, also known as CD300b, CD300LB, CLM-7, and IREM‑3, is a glycoprotein member of the immunoglobulin superfamily (1). Human LMIR5 consists of a 134 amino acid (aa) extracellular domain (ECD) with one Ig-like V-type domain, a 21 amino acid (aa) transmembrane segment, and a 29 aa cytoplasmic domain (2). Within the ECD, human LMIR5 shares 51 % sequence identity with mouse and 57% aa sequence identity with rat LMIR5. The transmembrane segment contains a positively charged lysine which enables the association of LMIR5 with DAP12, DAP10, and potentially other adaptor proteins (2, 3). The cytoplasmic domain of human LMIR5 contains a phosphorylatable tyrosine motif, while that of mouse LMIR5 does not (2). LMIR5 is expressed on the surface of myeloid lineage cells (2-4). It forms noncovalent cis‑homodimers and cis-heterodimers with other CD300 family proteins, and the composition of these dimers affects the cellular response (2, 5). Antibody cross‑linking of LMIR5 induces mast cell granule release and cytokine production as well as its tyrosine phosphorylation of LMIR5 (in human) (2, 3). LMIR5 interacts with TIM1 and TIM4 which regulate T cell activation and are themselves binding partners (6). TIM1 interactions with LMIR5 mediate mast cell activation and the accumulation of neutrophils at sites of TIM1 up‑regulation on damaged renal tubule epithelial cells (6).
  1. Clark, G.J. et al. (2009) Trends Immunol. 30:209.
  2. Martinez-Barriocanal, A. et al. (2006) J. Immunol. 177:2819.
  3. Yamanishi, Y. et al. (2008) Blood 111:688.
  4. Wu, Y. et al. (2011) Cell. Immunol. 268:68.
  5. Martinez-Barriocanal, A. et al. (2010) J. Biol. Chem. 285:41781.
  6. Yamanishi, Y. et al. (2010) J. Exp. Med. 207:1501.

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