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4-Ethynyl-1,1'-biphenyl
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4-Ethynyl-1,1'-biphenyl
Catalog Number:
(77124-398)
Supplier:
Prosci
Description:
Anti-H2-D1 Mouse Monoclonal Antibody [clone: [27-11-13S]] (PE (Phycoerythrin))
Supplier:
Ansell Healthcare
Description:
HyFlex® 11-581 industrial gloves feature an ultra-lightweight design, delivering 20% lighter EN ISO Cut F and ANSI/ISEA 105-2024 Cut A6 protection.
Catalog Number:
(100189-736)
Supplier:
Roboz Surgical
Description:
Pennington Forceps; Triangular Jaws; 6" Length
Supplier:
AMBEED, INC
Description:
3,6-Di-tert-butyl-9-mesityl-10-phenylacridin-10-ium tetrafluoroborate, Purity: 97%, CAS Number: 1810004-87-5, Appearance: Form: powder, crystalline Colour: light yellow to yellow, Storage: Keep in dark place, Inert atmosphere, Room temperature, Size: 5g
Catalog Number:
(10479-140)
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:
(10478-920)
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:
(10479-426)
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:
(10479-612)
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:
(ABCA_AB200486-500U)
Supplier:
ABCAM INC.
Description:
Anti-TMEM16A Mouse Monoclonal Antibody [clone: DG1/447 + DOG-1.1]
Supplier:
AOB CHEM USA
Description:
1-(2-(3-fluoro-2-methylphenoxy)ethyl)piperidine ≥97%
Supplier:
AMBEED, INC
Description:
4-Bromo-o-toluonitrile 98%
Catalog Number:
(76293-754)
Supplier:
United Scientific Supplies
Description:
These solid black stoppers are made of solid natural rubber that stays pliable over a long period of time.
Supplier:
AMBEED, INC
Description:
Diphenyl(trifluoromethyl)sulfonium trifluoromethanesulfonate 97%
Catalog Number:
(101935-786)
Supplier:
Matrix Scientific
Description:
MF=C10H17Cl2N3 MW=250.17 250Mg
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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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