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3-([1,1'-Biphenyl]-4-ylmethoxy)azetidine
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3-([1,1'-Biphenyl]-4-ylmethoxy)azetidine
Supplier:
AMBEED, INC
Description:
2-Methyl-1-((4-(6-(trifluoromethyl)pyridin-2-yl)-6-((2-(trifluoromethyl)pyridin-4-yl)amino)-1,3,5-triazin-2-yl)amino)propan-2-ol, Purity: 98%, CAS Number: 1446502-11-9, Appearance: White to Yellow Solid, Storage: Keep in dark place, Inert atmosphere, 2-8 C, Size: 5mg
Supplier:
AOB CHEM USA
Description:
2-Chloro-3-methoxy-4-pyridinecarboxamide ≥97%
Catalog Number:
(103406-868)
Supplier:
Novus Biologicals
Description:
The CD79B Antibody (HM79-11) [DyLight 488] from Novus Biologicals is a armenian hamster monoclonal antibody to CD79B. This antibody reacts with mouse. The CD79B Antibody (HM79-11) [DyLight 488] has been validated for the following applications: Western Blot, Flow Cytometry, Immunohistochemistry, Immunohistochemistry-Frozen.
Catalog Number:
(EM8.04104.1000)
Supplier:
AOB CHEM USA
Description:
4-Benzyloxy-3,5-dichlorobenzaldehyde ≥95%
Catalog Number:
(103620-156)
Supplier:
Sino Biological
Description:
This antibody was produced from a hybridoma resulting from the fusion of a mouse myeloma with B cells obtained from a mouse immunized with purified, recombinant Human KLK11 / Kallikrein 11 (rh KLK11 / Kallikrein 11; Catalog#10767-H08H; Met 1-Asn 250; NP_006844.1). The IgG fraction of the cell culture supernatant was purified by Protein A affinity chromatography.
Supplier:
Bachem Americas
Description:
25mg CAS: 51165-09-4 C41H60N10O9S FW: 869.06 . Substance P
Supplier:
TCI America
Description:
CAS Number: 2809-21-4
MDL Number: MFCD00070585 Molecular Formula: C2H8O7P2 Molecular Weight: 206.03 Form: Clear Liquid Color: Colorless Boiling point (°C): 105 Melting point (°C): -40 Specific Gravity (20/20): 1.45
Catalog Number:
(103231-288)
Supplier:
Novus Biologicals
Description:
CTCF, Polyclonal Antibody, Host: Sheep, Species reactivity: Human, Isotype: IgG, Immunogen: E. Coli-derived recombinant human CTCF, Synonyms: 11-zinc finger protein, 11-Zinc Finger Protein2, CTCFL paralog, Concentration: LYOPH, Application: Western Blot, Size: 25ug
Catalog Number:
(77055-442)
Supplier:
ANTIBODIES.COM LLC
Description:
Rabbit polyclonal antibody to Sox-11 for WB and ELISA with samples derived from Human, Mouse and Rat.
Catalog Number:
(89276-298)
Supplier:
Genetex
Description:
Mouse Monoclonal antibody to CD163 Clone: 2A10/11 Species Reactivity: Pig Tested Applications: FACS Pkg Size: 100 test
Catalog Number:
(76120-292)
Supplier:
Bioss
Description:
C11orf71, also known as FLJ20010, is a 123 amino acid protein that exists as two alternatively spliced isoforms and is encoded by a gene located on human chromosome 11. With approximately 135 million base pairs and 1400 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.
Catalog Number:
(76120-282)
Supplier:
Bioss
Description:
C11orf57, also known as FLJ10726, is a 292 amino acid protein that exists as three alternatively spliced isoforms and is encoded by a gene located on human chromosome 11. With approximately 135 million base pairs and 1400 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.
Catalog Number:
(76120-284)
Supplier:
Bioss
Description:
C11orf57, also known as FLJ10726, is a 292 amino acid protein that exists as three alternatively spliced isoforms and is encoded by a gene located on human chromosome 11. With approximately 135 million base pairs and 1400 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.
Catalog Number:
(76706-570)
Supplier:
AFG BIOSCIENCE LLC
Description:
Rat Cytochrome P450, Family 11, Subfamily A, Polypeptide 1(CYP11A1/Cytochrome P450scc) ELISA Kit
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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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