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4-Ethynyl-1,1'-biphenyl
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4-Ethynyl-1,1'-biphenyl
Supplier:
APOLLO SCIENTIFIC
Description:
5-Bromopicolinic acid 97%
Catalog Number:
(AA40608-04)
Catalog Number:
(75909-086)
Supplier:
Biotium
Description:
CD99 Monoclonal antibody, Clone: HO36-1.1, Host: Mouse, Species reactivity: Human, Rat, Isotype: IgG1, kappa, Conjugate: BSA-free, Immunogen: Purified E-rosette forming cells from human peripheral blood lymphocytes, Synonyms: MIC2, Application: IF, IHC, FC, Size: 50uL
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.
Catalog Number:
(102997-262)
Supplier:
Anaspec Inc
Description:
A hallmark of Alzheimer's disease (AD) is the presence of beta-Amyloid in plaques in the brains of patients. N-terminally truncated pyroglutamate-modified beta-Amyloid forms such as Aß(3-40) and Aß (11- 40) have been described as major compounds in the senile plaques. Pyro-Glu modified beta-Amyloid forms are more resistant to degradation, show higher toxicity and have increased aggregation propensity compared to non-modified beta-Amyloid.
Sequence: Pyr-VHHQKLVFFAEDVGSNKGAIIGLMVGGVV Molecular Weight: 3133.7 Da % Peak Area by HPLC: ≥95 Peptide Content: ≥ 60% Storage condition: -20°C
Supplier:
Sklar
Description:
All Sklar products are industry standard.
Supplier:
AMBEED, INC
Description:
L-Tyrosine benzyl ester p-toluenesulfonate salt, Purity: 98%, CAS number: 53587-11-4, Appearance: White to yellow powder or crystals, Storage: Inert atmosphere, Store in freezer, under -20C, Size: 25G
Catalog Number:
(TCC2268-1G)
Supplier:
TCI America
Description:
CAS Number: 55804-66-5
MDL Number: MFCD00051334 Molecular Formula: C18H19NO4 Molecular Weight: 313.35 Purity/Analysis Method: >98.0% (HPLC,N) Form: Crystal Melting point (°C): 150 Lambda max.: 436 nm (EtOH)
Supplier:
BioCam Communications
Description:
These full-color detailed guides provide you with an incredible classroom tool.
Catalog Number:
(89282-910)
Supplier:
Genetex
Description:
Mouse Monoclonal antibody to Hepatitis C Virus (HCV) Core Antigen Clone: 11-B3 Species Reactivity: Virus Tested Applications: ELISA IHC-Fr WB Pkg Size: 100 ug
Supplier:
Thermo Scientific Chemicals
Description:
MDL: MFCD00008789
Beilstein Registry No.: 1702372
Supplier:
Matrix Scientific
Description:
1-METHYL-1H-PYRAZOLE-4-CARBALDEHYDE MF=C5H6N2O MW=110.12 CAS=25016-11-9 MDL=MFCD00460465
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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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