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1,2-Dichloropropane
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1,2-Dichloropropane
Supplier:
AMBEED, INC
Description:
4'-Propyl-biphenyl-4-amine, Purity: 97%, CAS Number: 60040-12-2, Appearance: Solid, Storage: Keep in dark place, Inert atmosphere, Room temperature, Size: 1G
Catalog Number:
(76121-098)
Supplier:
Bioss
Description:
PTD015 is a 122 amino acid protein that belongs to the UPF0366 family. Existing as three alternatively spliced isoforms, the PTD015 gene is conserved in dog, cow, mouse, rat, chicken and zebrafish, and maps to human chromosome 11q14.1. With approximately 135 million base pairs and 1400 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. 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. The PTD015 gene product has been provisionally designated PTD015 pending further characterization.
Catalog Number:
(76121-100)
Supplier:
Bioss
Description:
PTD015 is a 122 amino acid protein that belongs to the UPF0366 family. Existing as three alternatively spliced isoforms, the PTD015 gene is conserved in dog, cow, mouse, rat, chicken and zebrafish, and maps to human chromosome 11q14.1. With approximately 135 million base pairs and 1400 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. 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. The PTD015 gene product has been provisionally designated PTD015 pending further characterization.
Catalog Number:
(10298-132)
Supplier:
Bioss
Description:
GLYATL1 is a 302 amino acid mitochondrial acyltransferase that transfers the acyl group to the N-terminus of glycine. GLYATL1 can also conjugate a multitude of substrates to form a variety of N-acylglycines. A member of the glycine N-acyltransferase family, GLYATL1 exists as two alternatively spliced isoforms and is encoded by a gene that maps to human chromosome 11q12.1. Chromosome 11 houses over 1,400 genes and comprises nearly 4% of the human genome. Jervell and Lange-Nielsen syndrome, Jacobsen syndrome, Niemann-Pick disease, hereditary angioedema and Smith-Lemli-Opitz syndrome are associated with defects in genes that maps to chromosome 11.
Catalog Number:
(100503-664)
Supplier:
Electron Microscopy Sciences
Description:
Used in connective tissue staining procedures to stain collagen. Used in differential staining (Snodgress el al., Lab Invest. 26:329, 1972).
Supplier:
TCI America
Description:
CAS Number: 1623-93-4
MDL Number: MFCD00078658
Molecular Formula: C12H9ClO2S
Molecular Weight: 252.71
Purity/Analysis Method: <gt/>98.0% (GC)
Form: Crystal
Melting point (°C): 114
Supplier:
AMBEED, INC
Description:
Potassium cyclohexyltrifluoroborate 96%
Catalog Number:
(EM1.04593.0025)
Catalog Number:
(10476-512)
Supplier:
Bioss
Description:
The coiled-coil domain is a structural motif found in proteins that are involved in a diverse array of biological functions such as the regulation of gene expression, cell division, membrane fusion, and drug extrusion and delivery. CCDC83 (coiled-coil domain-containing protein 83), also known as HSD9, is 413 amino acid protein that exists as three alternatively spliced isoforms. The gene encoding CCDC83 maps to human chromosome 11, which houses over 1,400 genes and comprises nearly 4% of the human genome. Jervell and Lange-Nielsen syndrome, Jacobsen syndrome, Niemann-Pick disease, hereditary angioedema and Smith-Lemli-Opitz syndrome are associated with defects in genes that maps to chromosome 11.
Catalog Number:
(10072-876)
Supplier:
Prosci
Description:
CT-1 is a member of the IL-6 family of cytokines which also includes LIF, CNTF, OSM (Oncostatin M), IL-11, IL-6 and possibly NT-1/ BSF-3. CT-1 is a pleiotropic cytokine which is expressed in various tissues including the adult heart, skeletal muscle, ovary, colon, prostate and fetal lung and signals through the LIF receptor and the gp130 receptor subunit. CT-1 has the ability to induce cardiac myocyte hypertrophy, and enhances the survival of cardiomyocyte and different neuronal populations. Biologically active human CT-1 is synthesized as a 201 amino acid polypeptide lacking a hydrophobic N-terminal secretion signal sequence. Recombinant Human CT-1 is a 21.5 kDa protein consisting of 201 amino acid residues.
Supplier:
Thermo Scientific Chemicals
Description:
1g CAS: 114772-40-6, MDL: MFCD06657561
Supplier:
BeanTown Chemical
Description:
CAS: 13885-09-1
Solid; Molecular Formula: C24H19P; MW: 338.38
Catalog Number:
(103007-246)
Supplier:
Anaspec Inc
Description:
This is a scrambled TAT-NSF222scr fusion polypeptide. It is composed of 11 amino acids from the cell permeable human immunodeficiency virus TAT polypeptide, 3 glycines as a linker, followed by scrambled N-Ethyl-maleimide-sensitive factor (NSF) D1 domain. This peptide is used as a control for the TAT-NSF222 peptide.
Sequence: YGRKKRRQRRR-GGG-ENSFRFLADIFPAKAFPVRFE MW: 4214.9 Da % Peak area by HPLC: 95 Storage condition: -20°C
Catalog Number:
(103633-286)
Supplier:
Sino Biological
Description:
A DNA sequence encoding the Influenza A virus (A/duck/Eastern China/11/2009(H6N6)) hemagglutinin (AEF59343.1) (Met1-Arg344), termed as HA1, was expressed with a polyhistidine tag at the C-terminus.
Supplier:
BeanTown Chemical
Description:
CAS: 406-95-1; MDL No: MFCD00198018
UN No: UN3272; Haz Class: 3; Packing Group: II
Liquid; Linear Formula: CH3COOCH2CF3; Molecular Formula: C4H5F3O2; MW: 142.08
Flash point: 11°C (51°F)
Density (g/mL): 1.258
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 is still displayed and you need assistance, please call us at 1-800-932-5000.
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.
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
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