2-Amino-2-(3-bromophenyl)acetic+acid
Supplier:
TCI America
Description:
CAS Number: 27164-46-1
MDL Number: MFCD00056883 Molecular Formula: C14H14N8O4S3 Molecular Weight: 476.48 Purity/Analysis Method: >98.0% (HPLC,T) Form: Crystal Melting point (°C): 190 Specific rotation [a]20/D: -20 deg (C=10, H2O) Storage Temperature: 0-10°C
Supplier:
AMBEED, INC
Description:
4-Chloropicolinic acid, Purity: 98%, CAS number: 5470-22-4, Appearance: White to yellow powder or crystals, Storage: Keep in dark place, Sealed in dry, Room Temperature, Size: 100G
Supplier:
Matrix Scientific
Description:
MF=C6H4F3Ns MW=179.16 Cas=76041-72-0 MDL=MFCD00128893 25G
Catalog Number:
(BDH83625.400)
Supplier:
VWR International
Description:
Toluene ≥99.8%, HiPerSolv CHROMANORM® for HPLC, VWR Chemicals BDH®
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Supplier:
TCI America
Description:
CAS Number: 10351-19-6
MDL Number: MFCD00006424 Molecular Formula: C7H7NO2S Molecular Weight: 169.20 Purity/Analysis Method: >98.0% (T) Form: Crystal Color: White
Supplier:
Matrix Scientific
Description:
Matrix Scientific Part Number: 059130-1G , MDL Number: MFCD00489772
Catalog Number:
(11001-664)
Supplier:
Wako Life Sciences
Description:
The Autokit 3-Hb R1 Set is an in vitro assay for the quantitative determination of 3-hydroxybutyrate (3-HB) in serum or plasma.
Supplier:
TCI America
Description:
CAS Number: 3179-31-5
MDL Number: MFCD00005229 Molecular Formula: C2H3N3S Molecular Weight: 101.13 Purity/Analysis Method: >98.0% (GC,T) Form: Crystal Melting point (°C): 218
Supplier:
Diagnostic Biosystems
Description:
Complement 4d (C4d) is the most clinically used marker for humoral rejection. It is a degradation product of the activated complement factor C4b. Complement 4d is typically initiated by binding of antibodies to specific target molecules. Following activation and degradation of the C4 molecule, thio-ester groups are exposed, which allow transient, covalent binding of the degradation product Complement 4d to endothelial cell surfaces and extracellular matrix components of vascular basement membranes near the sites of C4 activation. Complement 4d is also found in intracytoplasmic vacuoles of endothelial cells. Covalent binding renders C4d a stable molecule that can easily be detected by immunohistochemistry.
Catalog Number:
(10665-060)
Supplier:
Bioss
Description:
The G protein-coupled receptor TGR5 is a 330-amino acid protein that is almost universally expressed in human tissues including heart, skeletal muscle, spleen, kidney, liver, small intestine, placenta, and leukocytes, but not in brain, colon (without mucosa), thymus, or lung. TGR5 is sensitive to bile acids and responds through a significant mechanism that coordinates energy homeostasis. Bile acids activate mitogen-activated protein (MAP) kinase pathways, specifically induce TGR5 internalization, promote an increase of guanosine 5'-O-3-thio-triphosphate binding in membrane fractions, and cause rapid intracellular cAMP production. Bile acids also provoke TGR5 to suppress macrophage functions. TGR5-controlled signaling pathways may be good candidates for drug targets to treat common metabolic diseases, such as obesity, type II diabetes, hyperlipidemia, and atherosclerosis.
Catalog Number:
(10665-126)
Supplier:
Bioss
Description:
The G protein-coupled receptor TGR5 is a 330-amino acid protein that is almost universally expressed in human tissues including heart, skeletal muscle, spleen, kidney, liver, small intestine, placenta, and leukocytes, but not in brain, colon (without mucosa), thymus, or lung. TGR5 is sensitive to bile acids and responds through a significant mechanism that coordinates energy homeostasis. Bile acids activate mitogen-activated protein (MAP) kinase pathways, specifically induce TGR5 internalization, promote an increase of guanosine 5'-O-3-thio-triphosphate binding in membrane fractions, and cause rapid intracellular cAMP production. Bile acids also provoke TGR5 to suppress macrophage functions. TGR5-controlled signaling pathways may be good candidates for drug targets to treat common metabolic diseases, such as obesity, type II diabetes, hyperlipidemia, and atherosclerosis.
Supplier:
TCI America
Description:
CAS Number: 2487-40-3
MDL Number: MFCD00031505 Molecular Formula: C5H4N4OS Molecular Weight: 168.17 Purity/Analysis Method: >80.0% (HPLC) Form: Crystal Color: Very Pale Yellow
Catalog Number:
(10665-044)
Supplier:
Bioss
Description:
The G protein-coupled receptor TGR5 is a 330-amino acid protein that is almost universally expressed in human tissues including heart, skeletal muscle, spleen, kidney, liver, small intestine, placenta, and leukocytes, but not in brain, colon (without mucosa), thymus, or lung. TGR5 is sensitive to bile acids and responds through a significant mechanism that coordinates energy homeostasis. Bile acids activate mitogen-activated protein (MAP) kinase pathways, specifically induce TGR5 internalization, promote an increase of guanosine 5'-O-3-thio-triphosphate binding in membrane fractions, and cause rapid intracellular cAMP production. Bile acids also provoke TGR5 to suppress macrophage functions. TGR5-controlled signaling pathways may be good candidates for drug targets to treat common metabolic diseases, such as obesity, type II diabetes, hyperlipidemia, and atherosclerosis.
Catalog Number:
(10665-058)
Supplier:
Bioss
Description:
The G protein-coupled receptor TGR5 is a 330-amino acid protein that is almost universally expressed in human tissues including heart, skeletal muscle, spleen, kidney, liver, small intestine, placenta, and leukocytes, but not in brain, colon (without mucosa), thymus, or lung. TGR5 is sensitive to bile acids and responds through a significant mechanism that coordinates energy homeostasis. Bile acids activate mitogen-activated protein (MAP) kinase pathways, specifically induce TGR5 internalization, promote an increase of guanosine 5'-O-3-thio-triphosphate binding in membrane fractions, and cause rapid intracellular cAMP production. Bile acids also provoke TGR5 to suppress macrophage functions. TGR5-controlled signaling pathways may be good candidates for drug targets to treat common metabolic diseases, such as obesity, type II diabetes, hyperlipidemia, and atherosclerosis.
Supplier:
Cambridge Isotope Labs Inc
Description:
Benzene-[D₆] (99.5% D) (Isotopic)
Catalog Number:
(10665-056)
Supplier:
Bioss
Description:
The G protein-coupled receptor TGR5 is a 330-amino acid protein that is almost universally expressed in human tissues including heart, skeletal muscle, spleen, kidney, liver, small intestine, placenta, and leukocytes, but not in brain, colon (without mucosa), thymus, or lung. TGR5 is sensitive to bile acids and responds through a significant mechanism that coordinates energy homeostasis. Bile acids activate mitogen-activated protein (MAP) kinase pathways, specifically induce TGR5 internalization, promote an increase of guanosine 5'-O-3-thio-triphosphate binding in membrane fractions, and cause rapid intracellular cAMP production. Bile acids also provoke TGR5 to suppress macrophage functions. TGR5-controlled signaling pathways may be good candidates for drug targets to treat common metabolic diseases, such as obesity, type II diabetes, hyperlipidemia, and atherosclerosis.
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