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3-[1,1\\\'-Biphenyl]-4-ylacrylic+acid
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3-[1,1\\\'-Biphenyl]-4-ylacrylic+acid
Supplier:
Honeywell Research Chemicals
Description:
Xylenol Orange tetrasodium salt, Analytical, indicator for metal titration, CAS Number: 3618-43-7, Synonym: 3, 3aE raised to 2 -Bis[N, N-bis(carboxymethyl)aminomethyl]-o-cresolsulfonephthalein tetrasodium salt, Complexometric Reagent, Size: 5G
Supplier:
Mettler Toledo
Description:
Combined glass pH electrodes for direct pH measurement and acid/base titrations in aqueous or non-aqueous media.
Supplier:
BeanTown Chemical
Description:
CAS: 134412-18-3; MDL No: MFCD12828121
Powder; Molecular Formula: C20H22F2; MW: 300.39
Melting Point: 68-69°
Supplier:
Bel-Art Products
Description:
Epoxy-coated steel wire baskets hold up under the most severe laboratory conditions and are handy for transporting and batch dipping glassware.
Catalog Number:
(77437-912)
Supplier:
Bioss
Description:
FIBIN (Fin bud initiation factor homolog) is a 211 amino acid protein involved in fin initiation in zebrafish. The human homolog is encoded by a gene that maps to chromosome 11, which makes up around 4% of human genomic DNA and is considered a gene and disease association dense chromosome. The chromosome 11 encoded Atm gene is important for regulation of cell cycle arrest and apoptosis following double strand DNA breaks. Atm mutation leads to the disorder known as ataxia-telangiectasia. The blood disorders Sickle cell anemia and _ thalassemia are caused by HBB gene mutations. Wilms' tumors, WAGR syndrome and Denys-Drash syndrome are associated with mutations of the WT1 gene. Jervell and Lange-Nielsen syndrome, Jacobsen syndrome, Niemann-Pick disease, hereditary angioedema and Smith-Lemli-Opitz syndrome are also associated with defects in chromosome 11.
Supplier:
BeanTown Chemical
Description:
CAS: 81477-94-3; MDL No: MFCD00134280
Powder; Linear Formula: (C6H5)2C=NCH2COOC(CH3)3; Molecular Formula: C19H21NO2 ; MW: 295.38
Melting Point: 114-115°
Catalog Number:
(10453-634)
Supplier:
Bioss
Description:
Mtvr1 is a 176 amino acid protein that exists as two alternatively spliced isoforms. Belonging to the FAM89 family, Mtvr1 is encoded by a gene that maps to human chromosome 11, which comprises approximately 4% of human genomic DNA and is considered a gene and disease association dense chromosome. The chromosome 11 encoded Atm gene is important for regulation of cell cycle arrest and apoptosis following double strand DNA breaks. Atm mutation leads to the disorder known as ataxia-telangiectasia. The blood disorders Sickle cell anemia and thalassemia are caused by HBB gene mutations, while Wilms' tumors, WAGR syndrome and Denys-Drash syndrome are associated with mutations of the WT1 gene. Jervell and Lange-Nielsen syndrome, Jacobsen syndrome, Niemann-Pick disease, hereditary angioedema and Smith-Lemli-Opitz syndrome are also associated with defects in chromosome 11-encoded genes.
Catalog Number:
(10453-630)
Supplier:
Bioss
Description:
Mtvr1 is a 176 amino acid protein that exists as two alternatively spliced isoforms. Belonging to the FAM89 family, Mtvr1 is encoded by a gene that maps to human chromosome 11, which comprises approximately 4% of human genomic DNA and is considered a gene and disease association dense chromosome. The chromosome 11 encoded Atm gene is important for regulation of cell cycle arrest and apoptosis following double strand DNA breaks. Atm mutation leads to the disorder known as ataxia-telangiectasia. The blood disorders Sickle cell anemia and thalassemia are caused by HBB gene mutations, while Wilms' tumors, WAGR syndrome and Denys-Drash syndrome are associated with mutations of the WT1 gene. Jervell and Lange-Nielsen syndrome, Jacobsen syndrome, Niemann-Pick disease, hereditary angioedema and Smith-Lemli-Opitz syndrome are also associated with defects in chromosome 11-encoded genes.
Catalog Number:
(10479-440)
Supplier:
Bioss
Description:
FAM168A is a 244 amino acid protein that exists as three alternatively spliced isoforms and is encoded by a gene that maps to human chromosome 11, which makes up around 4% of human genomic DNA and is considered a gene and disease association dense chromosome. The chromosome 11 encoded Atm gene is important for regulation of cell cycle arrest and apoptosis following double strand DNA breaks. Atm mutation leads to the disorder known as ataxia-telangiectasia. The blood disorders Sickle cell anemia and ∫ thalassemia are caused by HBB gene mutations. Wilms' tumors, WAGR syndrome and Denys-Drash syndrome are associated with mutations of the WT1 gene. Jervell and Lange-Nielsen syndrome, Jacobsen syndrome, Niemann-Pick disease, hereditary angioedema and Smith-Lemli-Opitz syndrome are also associated with defects in chromosome 11.
Catalog Number:
(10479-142)
Supplier:
Bioss
Description:
FAM168A is a 244 amino acid protein that exists as three alternatively spliced isoforms and is encoded by a gene that maps to human chromosome 11, which makes up around 4% of human genomic DNA and is considered a gene and disease association dense chromosome. The chromosome 11 encoded Atm gene is important for regulation of cell cycle arrest and apoptosis following double strand DNA breaks. Atm mutation leads to the disorder known as ataxia-telangiectasia. The blood disorders Sickle cell anemia and ∫ thalassemia are caused by HBB gene mutations. Wilms' tumors, WAGR syndrome and Denys-Drash syndrome are associated with mutations of the WT1 gene. Jervell and Lange-Nielsen syndrome, Jacobsen syndrome, Niemann-Pick disease, hereditary angioedema and Smith-Lemli-Opitz syndrome are also associated with defects in chromosome 11.
Catalog Number:
(80053-822)
Supplier:
MilliporeSigma
Description:
Major uterine luteolytic prostaglandin. A pulmonary vasoconstrictor. Inhibits nitric oxide production by the uterine tissue and increases uterine contractility.
Supplier:
TCI America
Description:
3,4-Difluoro-4'-(trans-4-ethylcyclohexyl)biphenyl, Purity: >98.0%(GC), CAS Number: 134412-18-3, Molecular Formula: C20H22F2, Molecular Weight: 300.39, Form: Crystal-Powder, Solid, Color: White - Almost white, Size: 5G
Catalog Number:
(103007-128)
Supplier:
Anaspec Inc
Description:
This peptide is b-Amyloid 17 to 24 amino acids fragment. Several lines of evidence indicate that a region centering around positions 17 to 20 amino acids is important for b-Amyloid fibril formation. Destabilization of a helix covering residues 11–24, in particular residues 17–24, is critical for alpha-helix to b-strand conversion and fibril formation.
Sequence: LVFFAEDV Molecular Weight: 939.1 Da % Peak Area by HPLC: ≥95 Peptide Content: ≥ 60% Storage condition: -20°C
Catalog Number:
(76118-698)
Supplier:
Bioss
Description:
Mtvr1 is a 176 amino acid protein that exists as two alternatively spliced isoforms. Belonging to the FAM89 family, Mtvr1 is encoded by a gene that maps to human chromosome 11, which comprises approximately 4% of human genomic DNA and is considered a gene and disease association dense chromosome. The chromosome 11 encoded Atm gene is important for regulation of cell cycle arrest and apoptosis following double strand DNA breaks. Atm mutation leads to the disorder known as ataxia-telangiectasia. The blood disorders Sickle cell anemia and thalassemia are caused by HBB gene mutations, while Wilms' tumors, WAGR syndrome and Denys-Drash syndrome are associated with mutations of the WT1 gene. Jervell and Lange-Nielsen syndrome, Jacobsen syndrome, Niemann-Pick disease, hereditary angioedema and Smith-Lemli-Opitz syndrome are also associated with defects in chromosome 11-encoded genes.
Supplier:
Ergomat
Description:
ERGOMAT Nitro mats are specifically designed to provide superior traction in excessively wet or oily working environments without sacrificing ergonomic comfort
Catalog Number:
(101933-694)
Supplier:
Matrix Scientific
Description:
3-Biphenyl-2-ylmethyl-1-ethylpiperazin-2-one
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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
is still displayed and you need assistance, please call us at 1-800-932-5000.
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