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Supplier:
New England Biolabs (NEB)
Description:
An E.coli strain that carries the cloned ZraI gene from Zoogloea ramigera 11, (S.K. Degtyarev).
Catalog Number:
(10265-750)
Supplier:
Bioss
Description:
MPPED2 (Metallophosphoesterase domain-containing protein 2), also known as C11orf8, FAM1B or 239FB, is a 294 amino acid protein. Expressed primarily in fetal brain tissue, MPPED2 is encoded by a gene that 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 stranded 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:
(77686-016)
Supplier:
AMBEED, INC
Description:
3-(Trifluoromethyl)bicyclo[1.1.1]pentan-1-amine hydrochloride 98%
Catalog Number:
(10479-442)
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.
Supplier:
Enzo Life Sciences
Description:
Beneficial effect in cardiovascular diseases and inflammation. Inhibits PGE2 formation from arachidonic acid in 3T3 fibroblats.
Catalog Number:
(77437-896)
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 FAM55A gene product has been provisionally designated FAM55A pending further characterization.
Catalog Number:
(10453-640)
Supplier:
Bioss
Description:
Receptor for interleukin-11. The receptor systems for IL6, LIF, OSM, CNTF, IL11 and CT1 can utilize IL6ST for initiating signal transmission. The IL11/IL11RA/IL6ST complex may be involved in the control of proliferation and/or differentiation of skeletogenic progenitor or other mesenchymal cells.
Supplier:
APOLLO SCIENTIFIC
Description:
N,N'-1,3-Phenylenedimaleimide 95%
Supplier:
TCI America
Description:
9,9-Dimethyl-2,7-bis[N-(m-tolyl)anilino]fluorene, Purity: >98.0%(HPLC)(N), CAS Number: 143886-11-7, Molecular Formula: C41H36N2, MW: 556.75, Synonyms: 9,9-Dimethyl-N,N-diphenyl-N,N-di(m-tolyl)fluorene-2,7-diamine, DMFL-TPD, Size: 1G
Supplier:
Biolegend
Description:
APC anti-mouse CD68 [FA-11]; Isotype: Rat IgG2a; Reactivity: Mouse; Apps: ICFC, FC; Size: 100 μg
Supplier:
AOB CHEM USA
Description:
6-Chloro-5-nitropyridine-3-boronic acid pinacol ester ≥95%
Catalog Number:
(ABCA_AB125884-100U)
Supplier:
ABCAM INC.
Description:
Anti-smooth muscle Myosin heavy chain 11 Rabbit Polyclonal Antibody
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:
Strem Chemicals Inc
Description:
CAS #: 68683-17-0. Size: 10g.
Catalog Number:
(102892-554)
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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.
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