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3-[1,1'-Biphenyl]-4-ylacrylic+acid
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3-[1,1'-Biphenyl]-4-ylacrylic+acid
Catalog Number:
(TCH0866-005G)
Supplier:
TCI America
Description:
CAS Number: 3562-73-0
MDL Number: MFCD00016859 Molecular Formula: C14H14O Molecular Weight: 198.27 Purity/Analysis Method: >98.0% (GC) Form: Crystal Melting point (°C): 96
Catalog Number:
(89158-728)
Supplier:
Enzo Life Sciences
Description:
Immunization and blocking peptide for Glutamic Acid Decarboxylase (GAD) antibody (BML-GC3208). The tetradecapeptide corresponds to the N-terminal residues 4-17 of rat GAD65. The sequence is wholly conserved human GAD65.
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.
Catalog Number:
(10268-874)
Supplier:
Bioss
Description:
The leucine-rich (LRR) repeat is a 20-30 amino acid motif that forms a hydrophobic å/∫ horseshoe fold, allowing it to accommodate several leucine residues within a tightly packed core. All LRR repeats contain a variable segment and a highly conserved segment, the latter of which accounts for 11 or 12 residues of the entire LRR motif. SLITRK5 (SLIT and NTRK-like family, member 5), also known as LRRC11 (leucine-rich repeat-containing protein 11), is a 958 amino acid single-pass type I membrane protein that contains 16 LRR repeats and belongs to the SLITRK family. Expressed at high levels in the cerebral cortex, but also present in areas of the spinal cord and medulla, SLITRK5 functions to suppress neurite outgrowth, thereby playing a regulatory role in neuronal function. The gene encoding SLITRK5 maps to human chromosome 13, which houses over 400 genes, such as BRCA2 and RB1, and comprises nearly 4% of the human genome. Trisomy 13, also known as Patau syndrome, is deadly and the few who survive past one year suffer from permanent neurologic defects, difficulty eating and vulnerability to serious respiratory infections.
Catalog Number:
(10282-406)
Supplier:
Bioss
Description:
TMEM16C is a 981 amino acid multi-pass membrane protein that is encoded by a gene which maps to chromosome 11. With approximately 135 million base pairs and 1,400 genes, chromosome 11 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, 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.
Catalog Number:
(10282-414)
Supplier:
Bioss
Description:
TMEM16C is a 981 amino acid multi-pass membrane protein that is encoded by a gene which maps to chromosome 11. With approximately 135 million base pairs and 1,400 genes, chromosome 11 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, 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.
Catalog Number:
(10282-412)
Supplier:
Bioss
Description:
TMEM16C is a 981 amino acid multi-pass membrane protein that is encoded by a gene which maps to chromosome 11. With approximately 135 million base pairs and 1,400 genes, chromosome 11 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, 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.
Supplier:
Matrix Scientific
Description:
Matrix Scientific Part Number: 051044-500MG , MDL Number: MFCD13561414
Catalog Number:
(103008-620)
Supplier:
Anaspec Inc
Description:
This peptide is histone H3 amino acid residues 1 to 21. It is phosphorylated at Thr-11 with a C-terminal GG linker, followed by a biotinylated lysine. The modification of Thr-11 via phosphorylation is processed by a number of enzymes, including protein kinase C-related kinase 1 (PRK1) and Serine/threonine-protein kinase Chk1. This has many important functions, such as the establishment of a novel chromatin marker for transcriptional regulation, and the regulation of DNA-damage induced transcriptional repression. Provided at >95% peptide purity, this peptide was dissolved in distilled water at 1 mg/ml and re-lyophilized to powder form.
Sequence:ARTKQTARKS-pT-GGKAPRKQLA-GGK(Biotin)-NH2 MW:2802.2 Da % peak area by HPLC:95 Storage condition:-20° C
Supplier:
Matrix Scientific
Description:
[2-(Biphenyl-4-yloxy)-1-cyclopropylethyl]amine hydrochloride
Supplier:
AMBEED, INC
Description:
t-Boc-N-Amido-PEG7-Amine ≥98%
Supplier:
Mettler Toledo
Description:
Combined glass pH electrodes for direct pH measurement and acid/base titrations in aqueous or non-aqueous media.
Catalog Number:
(101850-228)
Supplier:
Matrix Scientific
Description:
Matrix Scientific Part Number: 040814-500MG , MDL Number: MFCD05239177
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°
Supplier:
THERMO FISHER SCIENTIFIC CHEMICALS
Description:
Cesium acetate 99%, pure
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.
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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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