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2-Amino-2-(3-bromophenyl)acetic+acid


141,897  results were found

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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
MSDS SDS
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
Supplier:  VWR International
Description:   Toluene ≥99.8%, HiPerSolv CHROMANORM® for HPLC, VWR Chemicals BDH®
MSDS SDS
Product available on GSA Advantage®
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
MSDS SDS
Supplier:  Matrix Scientific
Description:   Matrix Scientific Part Number: 059130-1G , MDL Number: MFCD00489772

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.
MSDS SDS
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
MSDS SDS
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.

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:  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
MSDS SDS
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.

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)

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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Stock for this item is limited, but may be available in a warehouse close to you. Please make sure that you are logged in to the site so that available stock can be displayed. If the call is still displayed and you need assistance, please call us at 1-800-932-5000.
This product is marked as restricted and can only be purchased by approved Shipping Accounts. If you need further assistance, email VWR Regulatory Department at Regulatory_Affairs@vwr.com
-Additional Documentation May be needed to purchase this item. A VWR representative will contact you if needed.
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The original product is no longer available. The replacement shown is available.
This product is no longer available. Alternatives may be available by searching with the VWR Catalog Number listed above. If you need further assistance, please call VWR Customer Service at 1-800-932-5000.
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