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4-Ethynyl-1,1'-biphenyl
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4-Ethynyl-1,1'-biphenyl
Catalog Number:
(TS43859-0010)
Supplier:
THERMO FISHER SCIENTIFIC CHEMICALS
Description:
tert-Butyl-3-(trifluoromethylsulfonyloxy)-8-azabicyclo[3.2.1]oct-3-ene-8-carboxylate 95%
Catalog Number:
(76108-334)
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:
AMBEED, INC
Description:
3-(4,4,5,5-Tetramethyl-1,3,2-dioxaborolan-2-yl)-1-[tris(1-methylethyl)silyl]-1H-pyrrole, Purity: 98%, CAS Number: 365564-11-0, Appearance: Solid, Storage: Inert atmosphere, Store in freezer, under -20C, Size: 250MG
Supplier:
THERMO FISHER SCIENTIFIC CHEMICALS
Description:
3-(N-Boc-aminomethyl)-5-bromopyridine 97%
Catalog Number:
(140319-BL)
Supplier:
Biolegend
Description:
Brilliant Violet 510™ anti-mouse CD90.2 (Thy1.2) [53-2.1]; Isotype: Rat IgG2a, κ; Reactivity: Mouse, Does not react with Thy-1.1 (CD90.1); Apps: FC; Size: 125 μl
Catalog Number:
(IC10088101)
Supplier:
MP Biomedicals
Description:
Soluble in ethyl acetate (1% w/v-clear, colorless solution) and chloroform.
Catalog Number:
(101914-774)
Supplier:
Matrix Scientific
Description:
Matrix Scientific Part Number: 058420-500MG , MDL Number: MFCD00007538
Catalog Number:
(77439-538)
Supplier:
Bioss
Description:
Subunit of the 11S REG-gamma (also called PA28-gamma) proteasome regulator, a doughnut-shaped homoheptamer which associates with the proteasome. 11S REG-gamma activates the trypsin-like catalytic subunit of the proteasome but inhibits the chymotrypsin-like and postglutamyl-preferring (PGPH) subunits. Facilitates the MDM2-p53/TP53 interaction which promotes ubiquitination- and MDM2-dependent proteasomal degradation of p53/TP53, limiting its accumulation and resulting in inhibited apoptosis after DNA damage. May also be involved in cell cycle regulation. Mediates CCAR2 and CHEK2-dependent SIRT1 inhibition (PubMed:25361978).
Catalog Number:
(10114-098)
Supplier:
Prosci
Description:
Polyclonal, Host: Goat, Immunogen: SCNN1D antibody was raised against an 11 amino acid synthetic peptide near the C-Terminus of SCNN1D, Tested Applications: ELISA
Supplier:
TCI America
Description:
CAS Number: 34487-61-1
MDL Number: MFCD00066901 Molecular Formula: C19H14O5S Molecular Weight: 376.36 Form: Crystal Color: Yellow Red Boiling point (°C): 285
Catalog Number:
(101815-332)
Supplier:
Matrix Scientific
Description:
Matrix Scientific Part Number: 023095-500MG , MDL Number: MFCD08687537
Supplier:
Matrix Scientific
Description:
Matrix Scientific Part Number: 056340-1G , MDL Number: MFCD14698168
Supplier:
Matrix Scientific
Description:
Matrix Scientific Part Number: 058705-10G , MDL Number: MFCD00047209
Supplier:
TCI America
Description:
CAS Number: 71209-71-7
MDL Number: MFCD00100434 Molecular Formula: C13H18O Molecular Weight: 190.29 Purity/Analysis Method: >95.0% (GC) Form: Clear Liquid Boiling point (°C): 162 Specific Gravity (20/20): 0.96
Catalog Number:
(77669-470)
Supplier:
AMBEED, INC
Description:
Stachydrine hydrochloride ≥97%
Catalog Number:
(10453-632)
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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