Supplier >
6-Bromothiazolo[4,5-b]pyrazin-2-amine
Print…
You Searched For:
22,220 results were found
6-Bromothiazolo[4,5-b]pyrazin-2-amine
Catalog Number:
(10453-634)
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:
(10453-630)
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:
(76121-106)
Supplier:
Bioss
Description:
C11orf21 is a 132 amino acid cytoplasmic protein that is expressed exclusively in heart and is encoded by a gene located on human chromosome 11. Diseases associated with C11orf21 include Beckwith-Wiedemann Syndrome.
Supplier:
APOLLO SCIENTIFIC
Description:
Benzhydrylamine
Catalog Number:
(103007-748)
Supplier:
Anaspec Inc
Description:
This is a short fragment of the b-Amyloid peptide containing Histidine 13 and 14. Alzheimer’s beta amyloid peptides form A? ion channels in lipid bilayers. It is postulated that ion channel activity of A? is related to cytotoxic activity of A?. Small peptides that contain the amino acid sequence of the predicted mouth region of the A? channel pore can inhibit A? ion channel activity. And, Histidines 13 and 14 have been shown to be essential for the peptide to inhibit Alzheimer’s disease A? ion channel and cytotoxicity.
Sequence: EVHHQKL Molecular Weight: 890 Da % Peak Area by HPLC: ≥95 Peptide Content: ≥ 60% Storage condition: -20°C
Supplier:
BeanTown Chemical
Description:
CAS: 10026-11-6; EC No: 233-058-2; MDL No: MFCD00011306; RTECS: ZH7175000
UN No: UN2503; Haz Class: 8; Packing Group: III
Powder; Linear Formula: ZrCl4; MW: 233.03
Melting Point: 331° (sublimes)
Density (g/mL): 2.803
Moisture Sensitive
Supplier:
ABCAM INC.
Description:
Anti-Sialoadhesin/CD169 Rabbit Monoclonal Antibody [clone: EPR27102-11] (Alexa Fluor® 568)
Catalog Number:
(76502-876)
Supplier:
SCAT AMERICAS, INC.
Description:
Dovetail the SymLine® system to suit specific requirements. This product selection includes several useful ancillaries.
Catalog Number:
(10195-784)
Supplier:
Sklar
Description:
Foss Intestinal Forceps are industry standard.
Catalog Number:
(76436-500)
Supplier:
Janitorial Supplies
Description:
Light-duty freestanding plastic T-frame sign holder allows signs to be displayed where needed most.
Catalog Number:
(103327-318)
Supplier:
Novus Biologicals
Description:
The GNA11 Antibody from Novus Biologicals is a rabbit polyclonal antibody to GNA11. This antibody reacts with human. The GNA11 Antibody has been validated for the following applications: Western Blot.
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.
Supplier:
Honeywell Research Chemicals
Description:
Potassium iodide, Purity: greater than or equal to 99.0%, Grade: ACS reagent, Cas number: 7681-11-0, Molecular Formula: KI, Molar mass: 166 g/mol, Synonym: Laboratory Chemical, ACS Grade Salt, Container: Poly bottle, Appearance: White crystal, Size: 2.5kg
Catalog Number:
(10483-878)
Supplier:
Bioss
Description:
GLB1L3 is a 653 amino acid protein belonging to the glycosyl hydrolase 35 family. GLB1L3 exists as three alternatively spliced isoforms and is encoded by a gene that maps to human chromosome 11q25. 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. 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:
TCI America
Description:
CAS Number: 13166-10-4
MDL Number: MFCD00082572 Molecular Formula: C6H6N2 Molecular Weight: 106.13 Purity/Analysis Method: >98.0% (GC) Form: Clear Liquid Boiling point (°C): 112 Flash Point (°C): 101 Specific Gravity (20/20): 0.96 Storage Temperature: 0-10°C
Inquire for Price
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.
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
-Additional Documentation May be needed to purchase this item. A VWR representative will contact you if needed.
This product has been blocked by your organization. Please contact your purchasing department for more information.
The original product is no longer available. The replacement shown is available.
This product is no longer available. Alternatives may be available by searching with the VWR Catalog Number listed above. If you need further assistance, please call VWR Customer Service at 1-800-932-5000.
|
|||||||||
List View
