Recombinant Human LILRB2/CD85d/ILT4 His-tag Avi Protein, CF Summary
Additional Information |
Biotinylated (HEK293-expressed) |
Details of Functionality |
Measured by its binding ability in a functional ELISA. When Biotinylated Recombinant Human LILRB2/CD85d/ILT4 His-tag Avi-tag (Catalog # AVI8429) is captured on EvenCoat Streptavidin Coated Plates (Catalog #
CP004) at 2 μg/mL (100 µL/well), the concentration of Recombinant Human Angiopoietin-like 7 Protein
(Catalog #
914-AN) that produces 50% of the binding response is 0.100-0.800 μg/mL. |
Source |
Human embryonic kidney cell, HEK293-derived human LILRB2/CD85d/ILT4 protein Human LILRB2/CD85d/ILT4 (Gln22-His458) Accession # Q8N423.4 | 6-His tag | Avi-tag | N-terminus | | C-terminus | |
|
Accession # |
|
N-terminal Sequence |
Gln22 inferred from enzymatic pyroglutamate treatment revealing Thr23 |
Structure / Form |
|
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 |
|
Theoretical MW |
50 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 |
65-75 kDa, under 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 with Trehalose. |
Purity |
>95%, by SDS-PAGE visualized with Silver Staining and quantitative densitometry by Coomassie® Blue Staining. |
Reconstitution Instructions |
Reconstitute at 500 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 LILRB2/CD85d/ILT4 His-tag Avi Protein, CF
Background
Immunoglobulin-like transcript 4 (ILT4), also
known as Leukocyte immunoglobulin-like receptor subfamily B member 2 (LILRB2) and
LIR2, is a member of a family of activating and inhibitory type immunoreceptors
mainly expressed in myeloid cells. The LILRB family contains five members,
LILRB1–5, with a varying number of Ig‑like domains in their extracellular
domains (ECD) that play roles in human immunity and are considered immune
checkpoint factors (1). Mature human ILT4 consists of an ECD with 4 Ig‑like
domains, a transmembrane segment, and a cytoplasmic domain with
3 inhibitory immunoreceptor tyrosine-based inhibitory motifs (ITIMs). The
ECD of human ILT4 shares 76% amino acid sequence identity with chimpanzee
ILT4. While relatives of ILT4s exist in birds and mammals, ILT4 homologs are
not found in lower organisms (2). ILT4 is primarily expressed by monocytes,
macrophages, and dendritic cells and binds to classical MHC I proteins as
well as the non-classical HLA-G1 and HLA-F molecules (3,4). ILT4 appears to modulate
immune responses during mid- and late-activation phases of the neutrophil
lifecycle. ILT4 activation promotes the development of tolerogenic dendritic
cells and the subsequent induction of regulatory T cells and CD4+ T cell anergy (5). ILT4 is also highly expressed in
various solid tumors and is a potent driver for tumor growth, invasion and
metastasis, and blocking ILT4 in tumor cells might be an effective strategy for
cancer therapy (6). Our Avi-tag Biotinylated ILT4 features biotinylation at a
single site contained within the Avi-tag, a unique 15 amino acid peptide. Protein orientation will be uniform when
bound to streptavidin-coated surface due to the precise control of
biotinylation and the rest of the protein is unchanged so there is no
interference in the protein's bioactivity.
- Kang, X. et al. (2016) Cell cycle 15:25.
- Dennis, G. et al. (2000) Proc. Natl. Acad. Sci. U.S.A. 97:13245.
- Baudhuin, J. et al. (2013) Proc. Natl. Acad. Sci. U.S.A. 110:17957.
- Shiroishi, M. et al. (2003) Proc. Natl. Acad. Sci. U.S.A. 100:8856.
- Wu, J. and Horuzsko, A. (2009) Human immunology 70:353.
- Chen, H.M. et al. (2018) J. Clin. Invest. 128:5647.
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