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FLUO+3\/AM
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FLUO+3\/AM
Catalog Number:
(TS20103-1000)
Supplier:
THERMO FISHER SCIENTIFIC CHEMICALS
Description:
Diisobutylaluminium hydride 1.1 M in cyclohexane, AcroSealâ„¢
Catalog Number:
(102844-896)
Supplier:
Matrix Scientific
Description:
5-Amino-3-(methylthio)-1-phenyl-1H-pyrazole-4-carbonitrile ≥97%
Supplier:
Columbia Printing & Graphics
Description:
Autoclavable lab labels, 8.5×11", circular 0.5" diameter, to dilineate sterile environment, intended for petri dish.
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:
(BDH67005.400)
Supplier:
VWR International
Description:
BDH* Methyl t-Butyl Ether, Chemical Formula: (CH3)3COCH3, Melting Point:, Boiling Point:, Flash Point: -32 deg C, Formula Weight:, CAS Number: 1634-04-4, Grade: HPLC/Spectro, HiPerSolv CHROMANORM, Class: F, Size: 4L
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.
Catalog Number:
(75834-824)
Supplier:
Restek
Description:
Standard Atlantic RBCA EPH Mix, 11 components, Concentration: 1,000 ug/mL each in hexane:methylene chloride (85:15), Minimum shelf life: 6 months, Volume: 1ml/ampule
Supplier:
THERMO FISHER SCIENTIFIC CHEMICALS
Description:
4-Pentyn-2-ol 97+%
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.
Supplier:
AOB CHEM USA
Description:
1-Bromo-4-chloro-2-isopropoxy-3-methylbenzene ≥97%
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.
Catalog Number:
(77626-892)
Supplier:
AMBEED, INC
Description:
4-Pyridineethanethiol hydrochloride ≥98%
Supplier:
Enzo Life Sciences
Description:
PPARgamma activator
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.
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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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