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5,5\\\'-Diallyl-2,2\\\'-dihydroxybiphenyl+(Magnolol)
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5,5\\\'-Diallyl-2,2\\\'-dihydroxybiphenyl+(Magnolol)
Catalog Number:
(BT133460-1G)
Supplier:
BeanTown Chemical
Description:
CAS: 126705-22-4; MDL No: MFCD00190873
Powder; Molecular Formula: C19H17NO4; MW: 323.35
Catalog Number:
(76053-390)
Supplier:
VWR International
Description:
Security lock devices for upright freezer racks are secured with a lock included.
Catalog Number:
(10312-272)
Supplier:
Bioss
Description:
C5orf55
Supplier:
TCI America
Description:
CAS Number: 55589-62-3
MDL Number: MFCD00043833
Molecular Formula: C4H5NO4S
Molecular Weight: 201.24
Purity/Analysis Method: <gt/>98.0% (T)
Form: Crystal
Catalog Number:
(89412-256)
Supplier:
Wesco
Description:
Ergonomic drum handler power lift handles most 30, 55 or 85 gallon drums made of steel, fiber and poly.
Supplier:
Dickson
Description:
Recorders are ideal for monitoring long-term temperature trends in areas where proper temperatures are critical to product stability.
Catalog Number:
(10320-630)
Supplier:
Bioss
Description:
Zinc-finger proteins contain DNA-binding domains and have a wide variety of functions, most of which encompass some form of transcriptional activation or repression. The majority of zinc-finger proteins contain a Kr_ppel-type DNA binding domain and a KRAB domain, which is thought to interact with KAP1, thereby recruiting histone modifying proteins. HIC-2 (hypermethylated in cancer 2) possesses zinc finger motifs that are thought to be important for DNA-binding and also has a BTB/POZ domain at the N-terminus, which is thought to be important for protein-protein binding, as well as for the binding of transcription factors. HIC-2 is also known as Hic-3, HIC1-related gene on chromosome 22 or Zinc finger and BTB domain-containing protein 30, and is a 615 amino acid protein that is expressed as two isoforms produced by alternative splicing. HIC-2 is highly expressed in cerebellum and is localized to the nucleus in cells. HIC-2 contains a short amino acid sequence that is thought to interact with CtBP, a transcriptional repressor. The gene sequence associated with HIC-2 is thought to be a target for miRNAs (microRNAs) which are expressed in many cancers, suggesting that HIC-2 could possess tumor suppressor capabilities.
Catalog Number:
(10476-324)
Supplier:
Bioss
Description:
Chromosome 22 contains over 500 genes and about 49 million bases. Being the second smallest human chromosome, 22 contains a surprising variety of interesting genes. Phelan-McDermid syndrome, Neurofibromatosis type 2 and autism are associated with chromosome 22. A schizophrenia susceptibility locus has been identified on chromosome 22 and studies show that 22q11 deletion symptoms include a high incidence of schizophrenia. Translocations between chromosomes 9 and 22 may lead to the formation of the Philadelphia Chromosome and the subsequent production of the novel fusion protein, BCR-Abl, a potent cell proliferation activator found in several types of leukemia. CCDC134 (coiled-coil domain containing 134), also known as MGC21013 or FLJ22349, is a 229 amino acid protein encoded by a gene mapping to human chromosome 22.
Catalog Number:
(220025-248)
Supplier:
R&D Systems
Description:
The Recombinant Rat CX3CL1/Fractalkine (aa 22-100) Protein from R&D Systems is derived from E. coli. The Recombinant Rat CX3CL1/Fractalkine (aa 22-100) Protein has been validated for the following applications: Bioactivity.
Catalog Number:
(10310-204)
Supplier:
Bioss
Description:
C22orf37 (chromosome 22 open reading frame 37), also known as FLJ40542, is a 170 amino acid protein encoded by a gene located on human chromosome 22, which contains over 500 genes and about 49 million bases. As the second smallest human chromosome, chomosome 22 contains a wide variety of genes with numerous functions. Phelan-McDermid syndrome, Neurofibromatosis type 2 and autism are associated with chromosome 22. A schizophrenia susceptibility locus has been identified on chromosome 22 and studies show that 22q11 deletion symptoms include a high incidence of schizophrenia. Translocations between chromosomes 9 and 22 may lead to the formation of the Philadelphia Chromosome and the subsequent production of the novel fusion protein, BCR-Abl, a potent cell proliferation activator found in several types of leukemia.
Catalog Number:
(76108-240)
Supplier:
Bioss
Description:
Chromosome 22 contains over 500 genes and about 49 million bases. Being the second smallest human chromosome, 22 contains a surprising variety of interesting genes. Phelan-McDermid syndrome, Neurofibromatosis type 2 and autism are associated with chromosome 22. A schizophrenia susceptibility locus has been identified on chromosome 22 and studies show that 22q11 deletion symptoms include a high incidence of schizophrenia. Translocations between chromosomes 9 and 22 may lead to the formation of the Philadelphia Chromosome and the subsequent production of the novel fusion protein, BCR-Abl, a potent cell proliferation activator found in several types of leukemia. CCDC134 (coiled-coil domain containing 134), also known as MGC21013 or FLJ22349, is a 229 amino acid protein encoded by a gene mapping to human chromosome 22.
Catalog Number:
(102999-796)
Supplier:
Anaspec Inc
Description:
C-type Natriuretic Peptide (CNP), identified in 1990 and called C-type (in order to maintain the alphabetical nomenclature of natriuretic peptides), is the most highly conserved of natriuretic peptides between species. It is derived from a 126 amino acid preprohormone. CNP exists in two mature forms, one found in tissues, another in plasma and cerebrospinal fluid. It is present in high concentration of the vascular tree, especially the endothelium, central nervous tissues, and renal tubular cells. It is a powerful vasorelaxant and inhibitor of smooth muscle cell proliferation and may play a role in coagulation and fibrinogenesis by modulating endothelial cells.
Sequence:GLSKGCFGLKLDRIGSMSGLGC (Disulfide bridge: 6-22) MW:2197.7 Da %Peak area by HPLC:≥95% Storage condition: -20°C
Catalog Number:
(80060-316)
Supplier:
Chemglass
Description:
These PTFE adapters have an inner joint of the listed size.
Catalog Number:
(76098-860)
Supplier:
Bioss
Description:
C22orf43 (chromosome 22 open reading frame 43), also known as MGC33025 or MGC75009, is a 229 amino acid protein encoded by a gene located on human chromosome 22, which contains over 500 genes and about 49 million bases. As the second smallest human chromosome, chomosome 22 contains a wide variety of genes with numerous functions. Phelan-McDermid syndrome, Neurofibromatosis type 2 and autism are associated with chromosome 22. A schizophrenia susceptibility locus has been identified on chromosome 22 and studies show that 22q11 deletion symptoms include a high incidence of schizophrenia. Translocations between chromosomes 9 and 22 may lead to the formation of the Philadelphia Chromosome and the subsequent production of the novel fusion protein, BCR-Abl, a potent cell proliferation activator found in several types of leukemia.
Supplier:
ACROBIOSYSTEMS INC MS
Description:
Human CD3 epsilon & CD3 delta Heterodimer Protein, His Tag&Tag Free (MALS verified), ACROBiosystems
Supplier:
Miltex
Description:
Carbon steel and stainless steel surgical blades feature razor-sharp cutting edges for superior cutting and clean incisions
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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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