recombinant mouse fetuin b Search Results


fetuin b protein, mouse, recombinant  (TargetMol)
N/A
   Buy from Supplier
purified recombinant mouse fetuin-b protein  (Invigate GmbH)
90
Invigate GmbH purified recombinant mouse fetuin-b protein
Purified Recombinant Mouse Fetuin B Protein, supplied by Invigate GmbH, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/recombinant+mouse+fetuin+b/purified+recombinant+mouse+fetuin+b+protein/pm27733488-133-6-16
Average 90 stars, based on 1 article reviews
purified recombinant mouse fetuin-b protein - by Bioz Stars, 2026-09
90/100 stars
  Buy from Supplier
recombinant mouse fetuin b (rpb860mu0  (Cloud-Clone corp)
90
Cloud-Clone corp recombinant mouse fetuin b (rpb860mu0
Expression of <t>fetuin</t> <t>B</t> in HepG2 cells and mice. The levels of fetuin B mRNA and protein in HepG2 cells and cell culture supernatants increased with FFAs compared with controls. The levels of fetuin B mRNA and protein in mice increased in the HFD group compared with the SCD group. A: The mRNA levels: Control vs. FFAs (P < 0.001); B: The protein expression of fetuin B in HepG2 cells; C: The protein levels in the culture supernatants of HepG2 cells (P < 0.001); (HepG2 experiment) Results are the mean ± SD of three independent experiments, each repeated in triplicate. D: The hepatic mRNA level: SCD vs. HFD (P < 0.001); E: The hepatic protein expression; F: The serum levels (SCD vs. HFD, P = 0.010); (Mouse experiment) Results are the mean ± SD of three independent experiments (n = 6, each group).
Recombinant Mouse Fetuin B (Rpb860mu0, supplied by Cloud-Clone corp, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/recombinant+mouse+fetuin+b/recombinant+mouse+fetuin+b++rpb860mu0/pmc06456555-142-8-13
Average 90 stars, based on 1 article reviews
recombinant mouse fetuin b (rpb860mu0 - by Bioz Stars, 2026-09
90/100 stars
  Buy from Supplier
recombinant mouse fetuin b protein  (Elabscience Biotechnology)
N/A
Fetuin-B , also known as Fetuin-like protein IRL685 and FETUB , is a secreted protein which belongs to thefetuin family. Fetuin-B / FETUB contains twocystatin domains. Fetuin-B is a member of the fetuin family ,
   Buy from Supplier
recombinant mouse fetuin-b/fetub protein  (Elabscience Biotechnology)
N/A
Fetuin-B, also known as Fetuin-like protein IRL685 and FETUB, is a secreted protein which belongs to thefetuin family. Fetuin-B / FETUB contains twocystatin domains. Fetuin-B is a member of the fetuin family, part of the
   Buy from Supplier
recombinant mouse fetuin b fetub protein  (Elabscience)
N/A
   Buy from Supplier

Image Search Results


Expression of fetuin B in HepG2 cells and mice. The levels of fetuin B mRNA and protein in HepG2 cells and cell culture supernatants increased with FFAs compared with controls. The levels of fetuin B mRNA and protein in mice increased in the HFD group compared with the SCD group. A: The mRNA levels: Control vs. FFAs (P < 0.001); B: The protein expression of fetuin B in HepG2 cells; C: The protein levels in the culture supernatants of HepG2 cells (P < 0.001); (HepG2 experiment) Results are the mean ± SD of three independent experiments, each repeated in triplicate. D: The hepatic mRNA level: SCD vs. HFD (P < 0.001); E: The hepatic protein expression; F: The serum levels (SCD vs. HFD, P = 0.010); (Mouse experiment) Results are the mean ± SD of three independent experiments (n = 6, each group).

Journal: American Journal of Translational Research

Article Title: Fetuin B aggravates liver X receptor-mediated hepatic steatosis through AMPK in HepG2 cells and mice

doi:

Figure Lengend Snippet: Expression of fetuin B in HepG2 cells and mice. The levels of fetuin B mRNA and protein in HepG2 cells and cell culture supernatants increased with FFAs compared with controls. The levels of fetuin B mRNA and protein in mice increased in the HFD group compared with the SCD group. A: The mRNA levels: Control vs. FFAs (P < 0.001); B: The protein expression of fetuin B in HepG2 cells; C: The protein levels in the culture supernatants of HepG2 cells (P < 0.001); (HepG2 experiment) Results are the mean ± SD of three independent experiments, each repeated in triplicate. D: The hepatic mRNA level: SCD vs. HFD (P < 0.001); E: The hepatic protein expression; F: The serum levels (SCD vs. HFD, P = 0.010); (Mouse experiment) Results are the mean ± SD of three independent experiments (n = 6, each group).

Article Snippet: Vehicle (20 mM Tris-HCL, Invitrogen, Carlsbad, CA) or recombinant mouse fetuin B (RPB860Mu0, Cloud-Clone Corp., Houston, TX) was infused using s.c. implanted osmotic pumps (Alzet #1002, Durect Corp., CA) for the 10-day duration.

Techniques: Expressing, Cell Culture

Recombinant fetuin B aggravated hepatic lipid accumulation in HepG2 cells. Hepatocellular lipid accumulation and AMPK-/LXR-pathways were evaluated after the administration of recombinant fetuin B in HepG2 cells exposed to FFAs. A: Oil Red O staining: FFA vs. FFA + Rec FetB (200 × and 400 ×); B: Intercellular TG content (FFA vs. FFA + Rec FetB, P = 0.001); C: The expression of key proteins in the AMPK and LXR pathways; D: The mRNA levels of lipid metabolic enzymes; Rec FetB, Recombinant fetuin B. Results are the mean ± SD of three independent experiments, each repeated in triplicate.

Journal: American Journal of Translational Research

Article Title: Fetuin B aggravates liver X receptor-mediated hepatic steatosis through AMPK in HepG2 cells and mice

doi:

Figure Lengend Snippet: Recombinant fetuin B aggravated hepatic lipid accumulation in HepG2 cells. Hepatocellular lipid accumulation and AMPK-/LXR-pathways were evaluated after the administration of recombinant fetuin B in HepG2 cells exposed to FFAs. A: Oil Red O staining: FFA vs. FFA + Rec FetB (200 × and 400 ×); B: Intercellular TG content (FFA vs. FFA + Rec FetB, P = 0.001); C: The expression of key proteins in the AMPK and LXR pathways; D: The mRNA levels of lipid metabolic enzymes; Rec FetB, Recombinant fetuin B. Results are the mean ± SD of three independent experiments, each repeated in triplicate.

Article Snippet: Vehicle (20 mM Tris-HCL, Invitrogen, Carlsbad, CA) or recombinant mouse fetuin B (RPB860Mu0, Cloud-Clone Corp., Houston, TX) was infused using s.c. implanted osmotic pumps (Alzet #1002, Durect Corp., CA) for the 10-day duration.

Techniques: Recombinant, Staining, Expressing

LXR is a downstream target of AMPK. To clarify the relation between AMPK and LXR, pretreatment with LXR siRNA was applied in HepG2 cells exposed to FFA + recombinant fetuin B. Pretreatment with AMPK agonist (AICAR, 1 mM) was applied to HepG2 cells exposed to FFA + recombinant fetuin B. A: Intercellular TG content: FFA + Rec vs. FFA + Rec + siLXR (P = 0.003); B: The expression of key proteins in the AMPK and LXR pathways; C: The mRNA levels of lipid metabolic enzymes; D: Intercellular TG content: FFA + Rec FetB vs. FFA + Rec FetB + AICAR (P < 0.001); E: The expression of key proteins in the AMPK AND LXR pathways; F: The mRNA levels of lipid metabolic enzymes; Rec, Recombinant fetuin B; siLXR, siRNA LXR. Results are the mean ± SD of three independent experiments, each repeated in triplicate.

Journal: American Journal of Translational Research

Article Title: Fetuin B aggravates liver X receptor-mediated hepatic steatosis through AMPK in HepG2 cells and mice

doi:

Figure Lengend Snippet: LXR is a downstream target of AMPK. To clarify the relation between AMPK and LXR, pretreatment with LXR siRNA was applied in HepG2 cells exposed to FFA + recombinant fetuin B. Pretreatment with AMPK agonist (AICAR, 1 mM) was applied to HepG2 cells exposed to FFA + recombinant fetuin B. A: Intercellular TG content: FFA + Rec vs. FFA + Rec + siLXR (P = 0.003); B: The expression of key proteins in the AMPK and LXR pathways; C: The mRNA levels of lipid metabolic enzymes; D: Intercellular TG content: FFA + Rec FetB vs. FFA + Rec FetB + AICAR (P < 0.001); E: The expression of key proteins in the AMPK AND LXR pathways; F: The mRNA levels of lipid metabolic enzymes; Rec, Recombinant fetuin B; siLXR, siRNA LXR. Results are the mean ± SD of three independent experiments, each repeated in triplicate.

Article Snippet: Vehicle (20 mM Tris-HCL, Invitrogen, Carlsbad, CA) or recombinant mouse fetuin B (RPB860Mu0, Cloud-Clone Corp., Houston, TX) was infused using s.c. implanted osmotic pumps (Alzet #1002, Durect Corp., CA) for the 10-day duration.

Techniques: Recombinant, Expressing

Fetuin B knockdown attenuated hepatic lipid accumulation in HepG2 cells. Hepatocellular lipid accumulation and the AMPK-/LXR-pathways were evaluated after fetuin B knockdown in HepG2 cells exposed to FFAs. A: Oil Red O staining: FFA vs. FFA + siFetB (200 × and 400 ×); B: Intercellular TG content (P = 0.004); C: The expression of key proteins in the AMPK and LXR pathways; D: The mRNA levels of lipid metabolic enzymes; siFetB, siRNA fetuin B. Results are the mean ± SD of three independent experiments, each repeated in triplicate.

Journal: American Journal of Translational Research

Article Title: Fetuin B aggravates liver X receptor-mediated hepatic steatosis through AMPK in HepG2 cells and mice

doi:

Figure Lengend Snippet: Fetuin B knockdown attenuated hepatic lipid accumulation in HepG2 cells. Hepatocellular lipid accumulation and the AMPK-/LXR-pathways were evaluated after fetuin B knockdown in HepG2 cells exposed to FFAs. A: Oil Red O staining: FFA vs. FFA + siFetB (200 × and 400 ×); B: Intercellular TG content (P = 0.004); C: The expression of key proteins in the AMPK and LXR pathways; D: The mRNA levels of lipid metabolic enzymes; siFetB, siRNA fetuin B. Results are the mean ± SD of three independent experiments, each repeated in triplicate.

Article Snippet: Vehicle (20 mM Tris-HCL, Invitrogen, Carlsbad, CA) or recombinant mouse fetuin B (RPB860Mu0, Cloud-Clone Corp., Houston, TX) was infused using s.c. implanted osmotic pumps (Alzet #1002, Durect Corp., CA) for the 10-day duration.

Techniques: Staining, Expressing

LXR is a downstream target of AMPK. To confirm that LXR is a downstream target of AMPK, pretreatment with LXR agonist (GW3965, 5 μM) was applied to HepG2 cells exposed to FFA + Fetuin B siRNA. A: Intercellular TG content: FFA + Rec FetB vs. FFA + siFetB + GW3965 (P = 0.005); B: The expression of key proteins in the AMPK and LXR pathways; C: The mRNA levels of lipid metabolic enzymes; siFetB, siRNA fetuin B. Results are the mean ± SD of three independent experiments, each repeated in triplicate.

Journal: American Journal of Translational Research

Article Title: Fetuin B aggravates liver X receptor-mediated hepatic steatosis through AMPK in HepG2 cells and mice

doi:

Figure Lengend Snippet: LXR is a downstream target of AMPK. To confirm that LXR is a downstream target of AMPK, pretreatment with LXR agonist (GW3965, 5 μM) was applied to HepG2 cells exposed to FFA + Fetuin B siRNA. A: Intercellular TG content: FFA + Rec FetB vs. FFA + siFetB + GW3965 (P = 0.005); B: The expression of key proteins in the AMPK and LXR pathways; C: The mRNA levels of lipid metabolic enzymes; siFetB, siRNA fetuin B. Results are the mean ± SD of three independent experiments, each repeated in triplicate.

Article Snippet: Vehicle (20 mM Tris-HCL, Invitrogen, Carlsbad, CA) or recombinant mouse fetuin B (RPB860Mu0, Cloud-Clone Corp., Houston, TX) was infused using s.c. implanted osmotic pumps (Alzet #1002, Durect Corp., CA) for the 10-day duration.

Techniques: Expressing

Fetuin B knockdown attenuated hepatic lipogenesis in mice fed a HFD. Hepatic lipid accumulation and the AMPK-/LXR-pathways were evaluated after fetuin B knockdown in mice exposed to a HFD. A: H&E staining and Oil Red O staining: HFD vs. HFD + shRNA (400 ×); B: Intrahepatic TG content (P < 0.001); C: Serum TG (P = 0.003); D: Liver enzymes; E: Key protein expression of the AMPK and LXR pathways in mouse liver; F: The mRNA levels of lipid metabolic enzymes; ALT, alanine transaminase; AST, aspartate transaminase. Results are the mean ± SD of three independent experiments (n = 6, each group).

Journal: American Journal of Translational Research

Article Title: Fetuin B aggravates liver X receptor-mediated hepatic steatosis through AMPK in HepG2 cells and mice

doi:

Figure Lengend Snippet: Fetuin B knockdown attenuated hepatic lipogenesis in mice fed a HFD. Hepatic lipid accumulation and the AMPK-/LXR-pathways were evaluated after fetuin B knockdown in mice exposed to a HFD. A: H&E staining and Oil Red O staining: HFD vs. HFD + shRNA (400 ×); B: Intrahepatic TG content (P < 0.001); C: Serum TG (P = 0.003); D: Liver enzymes; E: Key protein expression of the AMPK and LXR pathways in mouse liver; F: The mRNA levels of lipid metabolic enzymes; ALT, alanine transaminase; AST, aspartate transaminase. Results are the mean ± SD of three independent experiments (n = 6, each group).

Article Snippet: Vehicle (20 mM Tris-HCL, Invitrogen, Carlsbad, CA) or recombinant mouse fetuin B (RPB860Mu0, Cloud-Clone Corp., Houston, TX) was infused using s.c. implanted osmotic pumps (Alzet #1002, Durect Corp., CA) for the 10-day duration.

Techniques: Staining, shRNA, Expressing

Recombinant fetuin B aggravated hepatic lipogenesis in HFD-fed mice. Hepatic lipid accumulation and the AMPK-/LXR-pathways were evaluated after the administration of recombinant fetuin B in mice exposed to a HFD. A: H&E staining and Oil Red O staining: HFD vs. HFD + Rec (400 ×); B: Intrahepatic TG content (P = 0.026); C: Serum TG (P = 0.011); D: Liver enzymes; E: Key protein expression of the AMPK and LXR pathways in mouse liver; F: The mRNA levels of lipid metabolic enzymes; ALT, alanine transaminase; AST, aspartate transaminase; Rec, Recombinant fetuin B. Results are the mean ± SD of three independent experiments (n = 6, each group).

Journal: American Journal of Translational Research

Article Title: Fetuin B aggravates liver X receptor-mediated hepatic steatosis through AMPK in HepG2 cells and mice

doi:

Figure Lengend Snippet: Recombinant fetuin B aggravated hepatic lipogenesis in HFD-fed mice. Hepatic lipid accumulation and the AMPK-/LXR-pathways were evaluated after the administration of recombinant fetuin B in mice exposed to a HFD. A: H&E staining and Oil Red O staining: HFD vs. HFD + Rec (400 ×); B: Intrahepatic TG content (P = 0.026); C: Serum TG (P = 0.011); D: Liver enzymes; E: Key protein expression of the AMPK and LXR pathways in mouse liver; F: The mRNA levels of lipid metabolic enzymes; ALT, alanine transaminase; AST, aspartate transaminase; Rec, Recombinant fetuin B. Results are the mean ± SD of three independent experiments (n = 6, each group).

Article Snippet: Vehicle (20 mM Tris-HCL, Invitrogen, Carlsbad, CA) or recombinant mouse fetuin B (RPB860Mu0, Cloud-Clone Corp., Houston, TX) was infused using s.c. implanted osmotic pumps (Alzet #1002, Durect Corp., CA) for the 10-day duration.

Techniques: Recombinant, Staining, Expressing