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1,3,5-Tri(1-naphthyl)benzene
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1,3,5-Tri(1-naphthyl)benzene
Catalog Number:
(101785-568)
Supplier:
Matrix Scientific
Description:
MF=C8H7F3 MW=160.14 Cas=6140-17-6 MDL=MFCD00075476 5G
Supplier:
THERMO FISHER SCIENTIFIC CHEMICALS
Description:
Triacetin (glycerol triacetate) 99%
Supplier:
AMBEED, INC
Description:
1-Bromo-2,3-difluorobenzene 97%
Supplier:
Matrix Scientific
Description:
MF=C7H3Brf3No2 MW=270.01 Cas=344-38-7 MDL=MFCD00014706 25G
Catalog Number:
(76120-184)
Supplier:
Bioss
Description:
C10orf140, also known as DLN-1, is an 827 amino acid protein that belongs to the DACH/dachshund family. C10orf140 contains a poly-Alanine region that is highly polymorphic. The gene encoding C10orf140 maps to human chromosome 10, which spans nearly 135 million base pairs, makes up approximately 4.5% of total DNA in cells and encodes nearly 1200 genes. Several protein-coding genes, including those that encode for chemokines, cadherins, excision repair proteins, early growth response factors (Egrs) and fibroblast growth receptors (FGFRs), are located on chromosome 10. Defects in some of the genes that map to chromosome 10 are associated with Charcot-Marie Tooth disease, Jackson-Weiss syndrome, Usher syndrome, nonsyndromatic deafness, Wolman's syndrome, Cowden syndrome, multiple endocrine neoplasia type 2 and porphyria.
Supplier:
AMBEED, INC
Description:
4-Isopropylbenzyl alcohol 98%
Catalog Number:
(76111-008)
Supplier:
Bioss
Description:
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. 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 FAM76B gene product has been provisionally designated FAM76B pending further characterization.
Supplier:
Spectrum Chemicals
Description:
Terephthalonitrile, Purity: 98%, Cas number: 623-26-7, Molecular Formula: C8H4N2, Molecular Weight: 128.13, Color/Form: White Solid Crystalline powder, Synonym: 1,4-Dicyanobenzene, Size: 25GM
Supplier:
Matrix Scientific
Description:
Matrix Scientific Part Number: 051270-500MG , MDL Number: MFCD10686579
Supplier:
BeanTown Chemical
Description:
CAS: 162046-61-9; MDL No: MFCD00052330
UN No: UN3265; Haz Class: 8; Packing Group: II
Liquid; Molecular Formula: C8H4ClF3O2 ; MW: 224.56
Density (g/mL): 1.435
Moisture Sensitive
Supplier:
MP Biomedicals
Description:
Soluble in water (20 mg/mL) or ethanol (5 mg/mL). Creates a bluish-red solution with a yellow fluorescence.
Catalog Number:
(ABCA_AB270162-100U)
Supplier:
ABCAM INC.
Description:
Anti-Histone H3 (tri methyl K27) Rabbit Monoclonal Antibody [clone: EPR18607] (Alexa Fluor® 488)
Catalog Number:
(ABCA_AB318648-100U)
Supplier:
ABCAM INC.
Description:
Anti-Histone H4 (tri methyl K20) Rabbit Monoclonal Antibody [clone: EPR17001(2)] (Alexa Fluor® 647)
Catalog Number:
(ABCA_AB284635-100U)
Supplier:
ABCAM INC.
Description:
Anti-Histone H3 (tri methyl K9) Rabbit Monoclonal Antibody [clone: EPR16601] (Alexa Fluor® 488)
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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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