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(Fluoromethyl)triphenylphosphonium+tetrafluoroborate
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(Fluoromethyl)triphenylphosphonium+tetrafluoroborate
Catalog Number:
(76066-628)
Supplier:
Prosci
Description:
For WB starting dilution is: 1:1000
Catalog Number:
(77566-116)
Supplier:
AMBEED, INC
Description:
Everolimus 98%
Catalog Number:
(76065-040)
Supplier:
Prosci
Description:
For WB starting dilution is: 1:1000
Catalog Number:
(76069-640)
Supplier:
Prosci
Description:
For WB starting dilution is: 1:1000
Catalog Number:
(76009-554)
Supplier:
Prosci
Description:
For WB starting dilution is: 1:1000
Supplier:
Adipogen
Description:
A cell-permeable, non-alkylating, non-thiol, adduct-forming, redox cycling quinone. Generates superoxide production and induces cell proliferation, apoptosis and necrosis in vitro. Redox cycling agent.
Supplier:
BeanTown Chemical
Description:
CAS: 303-98-0; EC No: 206-147-9; MDL No: MFCD00042919; RTECS: DK3900000
Powder; Molecular Formula: C59H90O4; MW: 863.34
Light Sensitive
Catalog Number:
(10288-616)
Supplier:
Bioss
Description:
CRTAC1 is a 661 amino acid secreted protein. CRTAC1 is O-glycosylated and contains one EGF-like domain and four FG-GAP repeats. Up-regulated in mesenchymal stem cells undergoing chondrogenic differentiation and also by growth factor BMP-4, CRTAC1 is found in the interterritorial matrix of articular deep zone cartilage. CRTAC1 is expressed as three isoforms produced by alternative splicing events. All isoforms are expressed in bone, cartilage and lung, while isoforms 1 and 2 are expressed in the brain. The gene that encodes CRTAC1 maps to human chromosome 10, which contains over 800 genes and 135 million nucleotides, making up nearly 4.5% of the human genome.
Supplier:
AMBEED, INC
Description:
3,5-Dimethoxyphenol, Purity: 96%, CAS Number: 500-99-2, Appearance: Solid or Semi-solid or liquid or lump, Storage: Inert atmosphere, Room Temperature, Size: 100g
Supplier:
AVANTOR PERFORMANCE MATERIALS US
Description:
For trace metals analysis, ICP, environmental, pharmaceutical and low metals.
Catalog Number:
(76009-806)
Supplier:
Prosci
Description:
May be involved in pre-mRNA splicing.
Catalog Number:
(10436-180)
Supplier:
Bioss
Description:
C10orf28 is a 792 amino acid protein that exists as three alternatively spliced isoforms. The gene encoding C10orf28 maps to human chromosome 10, which spans nearly 135 million base pairs, makes up approximately 4.5% of total DNA in cells and encodes nearly 1,200 genes. Several protein-coding genes, including those that encode for chemokines, cadherins, excision repair proteins, early growth response factors (Egrs) and fibroblast growth receptors (FGFRs), are located on chromosome 10. Defects in some of the genes that map to chromosome 10 are associated with Charcot-Marie Tooth disease, Jackson-Weiss syndrome, Usher syndrome, nonsyndromatic deafness, Wolman’s syndrome, Cowden syndrome, multiple endocrine neoplasia type 2 and porphyria.
Catalog Number:
(76120-302)
Supplier:
Bioss
Description:
CWF19L1 is a 538 amino acid protein belonging to the CWF19 family and exists as three alternatively spliced isoforms. CWF19L1 is encoded by a gene located on human chromosome 10, which spans nearly 135 million base pairs, makes up approximately 4.5% of total DNA in cells and encodes nearly 1,200 genes. Several protein-coding genes, including those that encode for chemokines, cadherins, excision repair proteins, early growth response factors (Egrs) and fibroblast growth receptors (FGFRs), are located on chromosome 10. Defects in some of the genes that map to chromosome 10 are associated with Charcot-Marie Tooth disease, Jackson-Weiss syndrome, Usher syndrome, nonsyndromatic deafness, Wolman's syndrome, Cowden syndrome, multiple endocrine neoplasia type 2 and porphyria.
Catalog Number:
(10479-412)
Supplier:
Bioss
Description:
FAM13C1, also known as FAM13C, is a 585 amino acid protein that belongs to the FAM13 family. Existing as three alternatively spliced isoforms, the gene encoding FAM13C1 maps to human chromosome 10, which contains over 800 genes, 135 million nucleotides and makes up nearly 4.5% of the human genome. PTEN is an important tumor suppressor gene located on chromosome 10 and, when defective, causes a genetic predisposition to cancer development known as Cowden syndrome. The chromosome 10 encoded gene ERCC6 is important for DNA repair and is linked to Cockayne syndrome which is characterized by extreme photosensitivity and premature aging. Tetrahydrobiopterin deficiency and a number of syndromes involving defective skull and facial bone fusion are also linked to chromosome 10. As with most trisomies, trisomy 10 is rare and is deleterious.
Supplier:
TCI America
Description:
CAS Number: 23680-84-4
MDL Number: MFCD00051734 Molecular Formula: C10H10ClN3O2 Molecular Weight: 239.66 Purity/Analysis Method: >98.0% (HPLC,N) Form: Crystal Melting point (°C): 302
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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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