Weight problems is a significant danger issue for sort 2 diabetes (T2D) though the causal hyperlinks stay unclear. A function shared by each circumstances nonetheless is systemic irritation and raised ranges of circulating fatty acids (FFA). It’s broadly believed that in overweight people genetically liable to T2D, elevated ranges of plasma FFA might contribute in the direction of the dying and dysfunction of insulin-producing pancreatic β-cells in a means of (gluco)lipotoxicity.
In assist of this, in vitro research have proven persistently that long-chain saturated fatty acids (LC-SFA) are poisonous to rodent β-cells throughout persistent publicity (> 24 h). Conversely, shorter chain SFA and unsaturated species are nicely tolerated, suggesting that toxicity depends on carbon chain size and/or double bond configuration. Regardless of the wealth of proof implicating lipotoxicity as a method of β-cell dying in rodents, the proof {that a} comparable course of happens in people is far much less substantial. Subsequently, the current examine has evaluated the results of persistent publicity to fatty acids of various chain size and diploma of saturation, on the viability of human β-cells in tradition.
We now have additionally studied the results of a mix of fatty acids and pro-inflammatory cytokines. Strikingly, we discover that LC-FFA don’t readily promote the demise of human β-cells and that they might even supply a measure of safety towards the poisonous results of pro-inflammatory cytokines. Subsequently, these findings indicate {that a} mannequin wherein elevated circulating LC-FFA play a direct function in mediating β-cell dysfunction and dying in people, could also be overly simplistic.
Enriching for human acute myeloid leukemia stem cells utilizing reactive oxygen species-based cell sorting
Isolation of leukemia stem cells presents a problem as a result of heterogeneity of the immunophenotypic markers generally used to establish blood stem cells. A number of research have reported that relative ranges of reactive oxygen species (ROS) can be utilized to complement for stem cell populations, suggesting a possible different to floor antigen-based strategies.
Right here, we describe a protocol to complement for stem cells from human acute myeloid leukemia specimens utilizing relative ranges of ROS. This protocol offers constant enrichment of leukemia stem cells. For full particulars on the use and execution of this protocol, please confer with Lagadinou et al. (2013) and Pei et al. (2018).
Substrate Stiffness, Cell Anisotropy, and Cell–Cell Contact Contribute to Enhanced Structural and Calcium Dealing with Properties of Human Embryonic Stem Cell-Derived Cardiomyocytes
Human pluripotent stem cell-derived cardiomyocytes (hPSC-CMs) will be utilized to know the mechanisms underlying the event and development of coronary heart illness, in addition to to develop higher interventions and coverings for this illness. Nonetheless, these cells are structurally and functionally immature, which undermines a few of their adequacy in modeling grownup coronary heart tissue.
Earlier research with immature cardiomyocytes have proven that altering substrate stiffness, cell anisotropy, and/or cell-cell contact can improve the contractile and structural maturation of hPSC-CMs. On this examine, the structural and calcium dealing with properties of human embryonic stem cell-derived cardiomyocytes (hESC-CMs) have been enhanced by publicity to a downselected mixture of those three maturation stimuli. First, hESC-CMs have been seeded onto substrates composed of two business formulations of polydimethylsiloxane (PDMS), Sylgard 184 and Sylgard 527, whose stiffness ranged from 5 kPa to 101 kPa. Upon analyzing the morphological and calcium transient properties of those cells, it was concluded {that a} 21 kPa substrate yielded cells with the best diploma of maturation.
Subsequent, these PDMS substrates have been microcontact-printed with laminin to pressure the classy cells into rod-shaped geometries utilizing line patterns that have been 12, 18, or 24 μm in width. We discovered that cells on the 18 and 24 μm sample widths had structural and useful properties that have been superior to these on the 12 μm sample.
The hESC-CMs have been then seeded onto these line-stamped surfaces at a density of 500 000 cells per 25-mm-diameter substrate, to allow the formation of cell-cell contacts at their distal ends. We found that this mixture of tradition circumstances resulted in cells that have been extra structurally and functionally mature than those who have been solely uncovered to at least one or two stimuli. Our outcomes recommend that downselecting a mix of mechanobiological stimuli may show to be an efficient technique of maturing hPSC-CMs in vitro.
Laser-Primarily based Hybrid Manufacturing of Endosseous Implants: Optimized Titanium Surfaces for Enhancing Osteogenic Differentiation of Human Mesenchymal Stem Cells
Additive manufacturing (AM) is turning into more and more vital within the orthopedic and dental sectors thanks to 2 main benefits: the potential of customized manufacturing and the combination of advanced buildings. Nonetheless, at smaller scales, floor circumstances of AM merchandise are usually not mastered. Quite a few non-fused powder particles give rise to roughness values (Sa) higher than 10 μm, thus limiting biomedical purposes for the reason that floor roughness of, e.g., metallic implants performs a significant function within the high quality and charge of osseointegration.
On this examine, an progressive hybrid machine combining AM and a femtosecond laser (FS) was used to acquire Ti6Al4V elements with biofunctional surfaces. In the course of the manufacturing course of, the FS laser beam “neatly” ablates the floor, leaving in its path nanostructures created by the laser/matter interplay. This step decreases the Sa from 11 to four μm and will increase the floor wettability.
The conduct of human mesenchymal stem cells was evaluated on these new AM+FS surfaces and in contrast with that on AM surfaces and likewise on polished surfaces. The variety of cells hooked up 24 h after plating is equal on all surfaces, however cell spreading is greater on AM+FS surfaces in contrast with their AM counterparts. In the long term (days 7 and 14), fibronectin and collagen synthesis improve on AM+FS surfaces versus AM alone.
Alkaline phosphatase exercise, osteocalcin manufacturing, and mineralization, markers of osteogenic differentiation, are considerably decrease on uncooked AM surfaces, whereas on the AM+FS specimens they show a degree equal to that on the polished floor. Total, these outcomes point out that utilizing an FS laser beam through the fabrication of AM elements optimizes floor morphology to favor osteoblastic differentiation.
CD1B, NT (CD1B, T-cell surface glycoprotein CD1b, CD1b) (APC) |
MBS6282862-5x02mL |
MyBiosource |
5x0.2mL |
EUR 4250 |
CD1B, NT (CD1B, T-cell surface glycoprotein CD1b, CD1b) (FITC) |
MBS6282864-02mL |
MyBiosource |
0.2mL |
EUR 980 |
CD1B, NT (CD1B, T-cell surface glycoprotein CD1b, CD1b) (FITC) |
MBS6282864-5x02mL |
MyBiosource |
5x0.2mL |
EUR 4250 |
CD1B, NT (CD1B, T-cell surface glycoprotein CD1b, CD1b) (Biotin) |
MBS6282863-02mL |
MyBiosource |
0.2mL |
EUR 980 |
CD1B, NT (CD1B, T-cell surface glycoprotein CD1b, CD1b) (Biotin) |
MBS6282863-5x02mL |
MyBiosource |
5x0.2mL |
EUR 4250 |
CD1B, NT (CD1B, T-cell surface glycoprotein CD1b, CD1b) (MaxLight 405) |
MBS6282866-01mL |
MyBiosource |
0.1mL |
EUR 980 |
CD1B, NT (CD1B, T-cell surface glycoprotein CD1b, CD1b) (MaxLight 405) |
MBS6282866-5x01mL |
MyBiosource |
5x0.1mL |
EUR 4250 |
CD1B, NT (CD1B, T-cell surface glycoprotein CD1b, CD1b) (MaxLight 490) |
MBS6282867-01mL |
MyBiosource |
0.1mL |
EUR 980 |
CD1B, NT (CD1B, T-cell surface glycoprotein CD1b, CD1b) (MaxLight 490) |
MBS6282867-5x01mL |
MyBiosource |
5x0.1mL |
EUR 4250 |
CD1B, NT (CD1B, T-cell surface glycoprotein CD1b, CD1b) (MaxLight 550) |
MBS6282868-01mL |
MyBiosource |
0.1mL |
EUR 980 |
CD1B, NT (CD1B, T-cell surface glycoprotein CD1b, CD1b) (MaxLight 550) |
MBS6282868-5x01mL |
MyBiosource |
5x0.1mL |
EUR 4250 |
CD1B, NT (CD1B, T-cell surface glycoprotein CD1b, CD1b) (MaxLight 650) |
MBS6282869-01mL |
MyBiosource |
0.1mL |
EUR 980 |
CD1B, NT (CD1B, T-cell surface glycoprotein CD1b, CD1b) (MaxLight 650) |
MBS6282869-5x01mL |
MyBiosource |
5x0.1mL |
EUR 4250 |
CD1B, NT (CD1B, T-cell surface glycoprotein CD1b, CD1b) (MaxLight 750) |
MBS6282870-01mL |
MyBiosource |
0.1mL |
EUR 980 |
CD1B, NT (CD1B, T-cell surface glycoprotein CD1b, CD1b) (MaxLight 750) |
MBS6282870-5x01mL |
MyBiosource |
5x0.1mL |
EUR 4250 |
CD1B (T-cell Surface Glycoprotein CD1b, CD1b) (AP) |
MBS6130433-01mL |
MyBiosource |
0.1(mL |
EUR 875 |
CD1B (T-cell Surface Glycoprotein CD1b, CD1b) (AP) |
MBS6130433-5x01mL |
MyBiosource |
5x0.1mL |
EUR 3800 |
CD1B (T-cell Surface Glycoprotein CD1b, CD1b) (AP) |
MBS6372872-01mL |
MyBiosource |
0.1mL |
EUR 920 |
CD1B (T-cell Surface Glycoprotein CD1b, CD1b) (AP) |
MBS6372872-5x01mL |
MyBiosource |
5x0.1mL |
EUR 3990 |
CD1B (T-cell Surface Glycoprotein CD1b, CD1b) (PE) |
MBS6372882-01mL |
MyBiosource |
0.1mL |
EUR 920 |
CD1B (T-cell Surface Glycoprotein CD1b, CD1b) (PE) |
MBS6372882-5x01mL |
MyBiosource |
5x0.1mL |
EUR 3990 |
CD1B (T-cell Surface Glycoprotein CD1b, CD1b) (PE) |
MBS6156948-01mL |
MyBiosource |
0.1(mL |
EUR 875 |
CD1B (T-cell Surface Glycoprotein CD1b, CD1b) (PE) |
MBS6156948-5x01mL |
MyBiosource |
5x0.1mL |
EUR 3800 |
CD1B (T-cell Surface Glycoprotein CD1b, CD1b) APC |
MBS6135736-01mL |
MyBiosource |
0.1(mL |
EUR 875 |
CD1B (T-cell Surface Glycoprotein CD1b, CD1b) APC |
MBS6135736-5x01mL |
MyBiosource |
5x0.1mL |
EUR 3800 |
CD1B (T-cell Surface Glycoprotein CD1b, CD1b) APC |
MBS6372873-01mL |
MyBiosource |
0.1mL |
EUR 920 |
CD1B (T-cell Surface Glycoprotein CD1b, CD1b) APC |
MBS6372873-5x01mL |
MyBiosource |
5x0.1mL |
EUR 3990 |
CD1B (T-cell Surface Glycoprotein CD1b, CD1b) (HRP) |
MBS6372876-01mL |
MyBiosource |
0.1mL |
EUR 920 |
CD1B (T-cell Surface Glycoprotein CD1b, CD1b) (HRP) |
MBS6372876-5x01mL |
MyBiosource |
5x0.1mL |
EUR 3990 |
CD1B (T-cell Surface Glycoprotein CD1b, CD1b) (HRP) |
MBS6151645-01mL |
MyBiosource |
0.1(mL |
EUR 875 |
CD1B (T-cell Surface Glycoprotein CD1b, CD1b) (HRP) |
MBS6151645-5x01mL |
MyBiosource |
5x0.1mL |
EUR 3800 |
CD1B (T-cell Surface Glycoprotein CD1b, CD1b) (FITC) |
MBS6372875-01mL |
MyBiosource |
0.1mL |
EUR 920 |
CD1B (T-cell Surface Glycoprotein CD1b, CD1b) (FITC) |
MBS6372875-5x01mL |
MyBiosource |
5x0.1mL |
EUR 3990 |
CD1B (T-cell Surface Glycoprotein CD1b, CD1b) (FITC) |
MBS6146342-01mL |
MyBiosource |
0.1(mL |
EUR 875 |
CD1B (T-cell Surface Glycoprotein CD1b, CD1b) (FITC) |
MBS6146342-5x01mL |
MyBiosource |
5x0.1mL |
EUR 3800 |
CD1B, NT (CD1B, T-cell surface glycoprotein CD1b, CD1b) (Azide free) (HRP) |
MBS6282865-02mL |
MyBiosource |
0.2mL |
EUR 980 |
CD1B, NT (CD1B, T-cell surface glycoprotein CD1b, CD1b) (Azide free) (HRP) |
MBS6282865-5x02mL |
MyBiosource |
5x0.2mL |
EUR 4250 |
CD1B (T-cell Surface Glycoprotein CD1b, CD1b) (Biotin) |
MBS6141039-01mL |
MyBiosource |
0.1(mL |
EUR 875 |
CD1B (T-cell Surface Glycoprotein CD1b, CD1b) (Biotin) |
MBS6141039-5x01mL |
MyBiosource |
5x0.1mL |
EUR 3800 |
CD1B (T-cell Surface Glycoprotein CD1b, CD1b) (Biotin) |
MBS6372874-01mL |
MyBiosource |
0.1mL |
EUR 920 |
CD1B (T-cell Surface Glycoprotein CD1b, CD1b) (Biotin) |
MBS6372874-5x01mL |
MyBiosource |
5x0.1mL |
EUR 3990 |
CD1B (T-cell Surface Glycoprotein CD1b, CD1b) (MaxLight 405) |
MBS6372877-01mL |
MyBiosource |
0.1mL |
EUR 920 |
CD1B (T-cell Surface Glycoprotein CD1b, CD1b) (MaxLight 405) |
MBS6372877-5x01mL |
MyBiosource |
5x0.1mL |
EUR 3990 |
CD1B (T-cell Surface Glycoprotein CD1b, CD1b) (MaxLight 490) |
MBS6372878-01mL |
MyBiosource |
0.1mL |
EUR 920 |
CD1B (T-cell Surface Glycoprotein CD1b, CD1b) (MaxLight 490) |
MBS6372878-5x01mL |
MyBiosource |
5x0.1mL |
EUR 3990 |
CD1B (T-cell Surface Glycoprotein CD1b, CD1b) (MaxLight 550) |
MBS6372879-01mL |
MyBiosource |
0.1mL |
EUR 920 |
CD1B (T-cell Surface Glycoprotein CD1b, CD1b) (MaxLight 550) |
MBS6372879-5x01mL |
MyBiosource |
5x0.1mL |
EUR 3990 |
CD1B (T-cell Surface Glycoprotein CD1b, CD1b) (MaxLight 650) |
MBS6372880-01mL |
MyBiosource |
0.1mL |
EUR 920 |
CD1B (T-cell Surface Glycoprotein CD1b, CD1b) (MaxLight 650) |
MBS6372880-5x01mL |
MyBiosource |
5x0.1mL |
EUR 3990 |
CD1B (T-cell Surface Glycoprotein CD1b, CD1b) (MaxLight 750) |
MBS6372881-01mL |
MyBiosource |
0.1mL |
EUR 920 |
CD1B (T-cell Surface Glycoprotein CD1b, CD1b) (MaxLight 750) |
MBS6372881-5x01mL |
MyBiosource |
5x0.1mL |
EUR 3990 |
CD1B (T-cell Surface Glycoprotein CD1b, CD1b) (MaxLight 490) |
MBS6199971-01mL |
MyBiosource |
0.1(mL |
EUR 875 |
CD1B (T-cell Surface Glycoprotein CD1b, CD1b) (MaxLight 490) |
MBS6199971-5x01mL |
MyBiosource |
5x0.1mL |
EUR 3800 |
CD1B (T-cell Surface Glycoprotein CD1b, CD1b) (MaxLight 550) |
MBS6210646-01mL |
MyBiosource |
0.1(mL |
EUR 875 |
CD1B (T-cell Surface Glycoprotein CD1b, CD1b) (MaxLight 550) |
MBS6210646-5x01mL |
MyBiosource |
5x0.1mL |
EUR 3800 |
CD1B (T-cell Surface Glycoprotein CD1b, CD1b) (MaxLight 405) |
MBS6189296-01mL |
MyBiosource |
0.1(mL |
EUR 875 |
CD1B (T-cell Surface Glycoprotein CD1b, CD1b) (MaxLight 405) |
MBS6189296-5x01mL |
MyBiosource |
5x0.1mL |
EUR 3800 |
CD1B (T-cell Surface Glycoprotein CD1b, CD1b) (MaxLight 650) |
MBS6221321-01mL |
MyBiosource |
0.1(mL |
EUR 875 |
CD1B (T-cell Surface Glycoprotein CD1b, CD1b) (MaxLight 650) |
MBS6221321-5x01mL |
MyBiosource |
5x0.1mL |
EUR 3800 |
CD1B (T-cell Surface Glycoprotein CD1b, CD1b) (MaxLight 750) |
MBS6231996-01mL |
MyBiosource |
0.1(mL |
EUR 875 |
CD1B (T-cell Surface Glycoprotein CD1b, CD1b) (MaxLight 750) |
MBS6231996-5x01mL |
MyBiosource |
5x0.1mL |
EUR 3800 |
CD1B |
CSB-CL004890HU |
Cusabio |
10 μg plasmid + 200μl Glycerol |
Ask for price |
CD1B |
pro-1267 |
ProSpec Tany |
2µg |
EUR 60 |
Description: Recombinant Human CD1B |
CD1b |
MBS438097-002mgWithBSAAzideat02mgmL |
MyBiosource |
0.02mg(WithBSA&Azideat0.2mg/mL) |
EUR 230 |
CD1b |
MBS438097-01mgWithBSAAzideat02mgmL |
MyBiosource |
0.1mg(WithBSA&Azideat0.2mg/mL) |
EUR 405 |
CD1b |
MBS438097-01mgWithoutBSAAzideat1mgmL |
MyBiosource |
0.1mg(WithoutBSA&Azideat1mg/mL) |
EUR 405 |
CD1b |
MBS438097-5x01mgWithBSAAzideat02mgmL |
MyBiosource |
5x0.1mg(WithBSA&Azideat0.2mg/mL) |
EUR 1725 |
CD1b |
MBS438097-5x01mgWithoutBSAAzideat1mgmL |
MyBiosource |
5x0.1mg(WithoutBSA&Azideat1mg/mL) |
EUR 1725 |
CD1B siRNA |
20-abx910943 |
Abbexa |
-
Ask for price
-
Ask for price
|
|
|
T-Cell Surface Glycoprotein CD1b (CD1B) Protein |
20-abx263315 |
Abbexa |
-
Ask for price
-
Ask for price
-
Ask for price
|
|
|
T-Cell Surface Glycoprotein CD1b (CD1B) Protein |
abx263315-10mg |
Abbexa |
10 mg |
EUR 325 |
T-Cell Surface Glycoprotein CD1b (CD1B) Protein |
abx263315-25mg |
Abbexa |
25 mg |
EUR 1600 |
T-Cell Surface Glycoprotein CD1b (CD1B) Protein |
abx263315-5mg |
Abbexa |
5 mg |
EUR 225 |
T-cell Surface Glycoprotein CD1b (CD1B) Antibody |
abx139084-01mg |
Abbexa |
0.1 mg |
EUR 427.2 |
|
T-cell Surface Glycoprotein CD1b (CD1B) Antibody |
20-abx006357 |
Abbexa |
-
Ask for price
-
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-
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-
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|
- 100 ul
- 200 ul
- 20 ul
- 50 ul
|
|
T-cell Surface Glycoprotein CD1b (CD1B) Antibody |
abx030324-400ul |
Abbexa |
400 ul |
EUR 627.6 |
|
T-cell Surface Glycoprotein CD1b (CD1B) Antibody |
abx030324-80l |
Abbexa |
80 µl |
EUR 343.2 |
|
T-cell Surface Glycoprotein CD1b (CD1B) Antibody |
20-abx009480 |
Abbexa |
-
Ask for price
-
Ask for price
-
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|
|
|
T-cell Surface Glycoprotein CD1b (CD1B) Antibody |
20-abx320708 |
Abbexa |
-
Ask for price
-
Ask for price
|
|
|
T-cell Surface Glycoprotein CD1b (CD1B) Antibody |
abx030324-400l |
Abbexa |
400 µl |
EUR 518.75 |
T-cell Surface Glycoprotein CD1b (CD1B) Antibody |
abx139084-100l |
Abbexa |
100 µl |
EUR 275 |
T-cell Surface Glycoprotein CD1b (CD1B) Antibody |
abx139084-500l |
Abbexa |
500 µl |
Ask for price |
T-cell Surface Glycoprotein CD1b (CD1B) Antibody |
abx320708-100l |
Abbexa |
100 µl |
EUR 350 |
T-cell Surface Glycoprotein CD1b (CD1B) Antibody |
abx320708-50l |
Abbexa |
50 µl |
EUR 250 |
T-cell Surface Glycoprotein CD1b (CD1B) Antibody |
abx006357-100g |
Abbexa |
100 µg |
EUR 275 |
T-cell Surface Glycoprotein CD1b (CD1B) Antibody |
abx006357-10g |
Abbexa |
10 µg |
EUR 175 |
T-cell Surface Glycoprotein CD1b (CD1B) Antibody |
abx006357-200g |
Abbexa |
200 µg |
EUR 400 |
CD1b antibody |
10R-6324 |
Fitzgerald |
100 ug |
EUR 260 |
|
Description: Mouse monoclonal CD1b antibody |
CD1B antibody |
22413 |
SAB |
100ul |
EUR 479 |
CD1B antibody |
22413-100ul |
SAB |
100ul |
EUR 468 |
CD1B Antibody |
46433 |
SAB |
100ul |
EUR 319 |
CD1B Antibody |
46433-100ul |
SAB |
100ul |
EUR 302.4 |
CD1B Antibody |
E046433 |
EnoGene |
100μg/100μl |
EUR 255 |
Description: Available in various conjugation types. |
CD1B Antibody |
E10-31418 |
EnoGene |
100ul |
EUR 225 |
Description: Available in various conjugation types. |
CD1B Antibody |
E10-31419 |
EnoGene |
100ul |
EUR 225 |
Description: Available in various conjugation types. |
CD1B Antibody |
E19-10150-1 |
EnoGene |
50ug/50ul |
EUR 145 |
Description: Available in various conjugation types. |
CD1B Antibody |
E19-10150-2 |
EnoGene |
100ug/100ul |
EUR 225 |
Description: Available in various conjugation types. |
CD1B Antibody |
E309888 |
EnoGene |
100ug/200ul |
EUR 295 |
Description: Available in various conjugation types. |
CD1B antibody |
70R-13508 |
Fitzgerald |
100 ul |
EUR 550 |
|
Description: Affinity purified Rabbit polyclonal CD1B antibody |
CD1b antibody |
70R-49494 |
Fitzgerald |
100 ul |
EUR 242 |
|
Description: Purified Polyclonal CD1b antibody |
CD1B Antibody |
1-CSB-PA004890ESR2HU |
Cusabio |
-
Ask for price
-
Ask for price
|
|
|
Description: A polyclonal antibody against CD1B. Recognizes CD1B from Human. This antibody is Unconjugated. Tested in the following application: ELISA, IHC; Recommended dilution: IHC:1:20-1:200 |
CD1b Antibody |
F46544-0.08ML |
NSJ Bioreagents |
0.08 ml |
EUR 140.25 |
|
Description: This gene encodes a member of the CD1 family of transmembrane glycoproteins, which are structurally related to the major histocompatibility complex (MHC) proteins and form heterodimers with beta-2-microglobulin. The CD1 proteins mediate the presentation of primarily lipid and glycolipid antigens of self or microbial origin to T cells. The human genome contains five CD1 family genes organized in a cluster on chromosome 1. The CD1 family members are thought to differ in their cellular localization and specificity for particular lipid ligands. The protein encoded by this gene localizes to late endosomes and lysosomes via a tyrosine-based motif in the cytoplasmic tail, and requires vesicular acidification to bind lipid antigens. [provided by RefSeq]. |
CD1b Antibody |
F46544-0.4ML |
NSJ Bioreagents |
0.4 ml |
EUR 322.15 |
|
Description: This gene encodes a member of the CD1 family of transmembrane glycoproteins, which are structurally related to the major histocompatibility complex (MHC) proteins and form heterodimers with beta-2-microglobulin. The CD1 proteins mediate the presentation of primarily lipid and glycolipid antigens of self or microbial origin to T cells. The human genome contains five CD1 family genes organized in a cluster on chromosome 1. The CD1 family members are thought to differ in their cellular localization and specificity for particular lipid ligands. The protein encoded by this gene localizes to late endosomes and lysosomes via a tyrosine-based motif in the cytoplasmic tail, and requires vesicular acidification to bind lipid antigens. [provided by RefSeq]. |
This new hybrid machine may make it attainable to provide AM implants with useful surfaces straight on the finish of AM, thereby limiting their post-treatments.