Keep my session open?
Ending In 
The session is expired
Your session has expired. For your security, we have logged you out.
Would you like to log in again?

Update to Avantor’s response to the coronavirus (COVID-19) pandemic

  • Product Results
  • Product Category
  • Criteria
  • Supplier
  • Refine by Suppliers
    Sort by:

  • Search Within Results

You Searched For:

Carbonyldiiodo(pentamethylcyclopentadienyl)cobalt(III)


8,801  results were found

SearchPresentationType-SearchPresentationType-SearchPresentationType-SearchPresentationType-SearchPresentationType-SearchPresentationType-SearchPresentationType-SearchPresentationType-SearchPresentationType-SearchPresentationType-SearchPresentationType-SearchPresentationType-SearchPresentationType-SearchPresentationType-SearchPresentationType-SearchPresentationType-SearchPresentationType-SearchPresentationType-SearchPresentationType-SearchPresentationType-SearchPresentationType-SearchPresentationType-SearchPresentationType-SearchPresentationType-SearchPresentationType-SearchPresentationType-SearchPresentationType-SearchPresentationType-SearchPresentationType-SearchPresentationType-SearchPresentationType-SearchPresentationType-SearchPresentationType-SearchPresentationType-SearchPresentationType-SearchPresentationType-SearchPresentationType-SearchPresentationType-SearchPresentationType-SearchPresentationType-SearchPresentationType-SearchPresentationType-SearchPresentationType-SearchPresentationType-SearchPresentationType-SearchPresentationType-SearchPresentationType-SearchPresentationType-SearchPresentationType-SearchPresentationType-SearchPresentationType-HORIZONTAL
 
 
SearchResultCount:"8801"
  List View Searching Easy View BETA(new)
Sort by:
 
 
 
 


Supplier:  Bioss
Description:   NCAM2 is an 837 amino acid protein encoded by the human gene NCAM2. NCAM2 contains five immunoglobulin-like domains, two Fibronectin type III domains, a transmembrane domain and a cytoplasmic domain. The gene is expressed most strongly in human adult and fetal brain. NCAM2 is a member of the neural cell adhesion molecule (NCAM) family. NCAMs are closely related cell surface glycoproteins involved in cell to cell interactions during growth and are thought to play an important role in embryogenesis and development. NCAM2 is a considered a good candidate for involvement in certain Down syndrome phenotypes because a slight overexpression of NCAMs increases many-fold the homotypic adhesion properties of cells. Stat5 regulates NCAM2 in vivo by binding to the NCAM2 intron in the NKL natural killer cell line; this binding is induced by cytokines that activate Stat5. Neither Stat1 nor Stat3 bind to this region, despite sharing a consensus binding sequence with Stat5.
Supplier:  New England Biolabs (NEB)
Description:   An <i>E. coli</i> strain that carries the HaeIII gene from Haemophilus aegypticus (ATCC 11116).
Small Business Enterprise
Catalog Number: (10349-920)

Supplier:  Bioss
Description:   The autosomal dominant cerebellar ataxias (ADCA) are a heterogeneous group of neurodegenerative disorders characterized by progressive degeneration of the cerebellum, brain stem and spinal cord. Clinically, ADCA has been divided into three groups: ADCA types I-III. ADCAI is genetically heterogeneous, with five genetic loci, designated spinocerebellar ataxia (SCA) 1, 2, 3, 4 and 6, being assigned to five different chromosomes. ADCAII, which always presents with retinal degeneration (SCA7), and ADCAIII often referred to as the `pure' cerebellar syndrome (SCA5), are most likely homogeneous disorders. Several SCA genes have been cloned and shown to contain CAG repeats in their coding regions. ADCA is caused by the expansion of the CAG repeats, producing an elongated polyglutamine tract in the corresponding protein. The expanded repeats are variable in size and unstable, usually increasing in size when transmitted to successive generations. The function of the ataxins is not known. This locus has been mapped to chromosome 6, and it has been determined that the diseased allele contains41-81 CAG repeats, compared to 6-39 in the normal allele, and is associated with spinocerebellar ataxia type 1 (SCA1). At least two transcript variants encoding the same protein have been found for this gene. [provided by RefSeq].
Supplier:  BeanTown Chemical
Description:   CAS: 7446-70-0; EC No: 231-208-1; MDL No: MFCD00003422; RTECS: BD0525000 UN No: UN1726; Haz Class: 8; Packing Group: II Powder/Lump; Molecular Formula: AlCl3; MW: 133.34 Melting Point: 190° Moisture Sensitive
MSDS SDS
Catalog Number: (101094-900)

Supplier:  USP
Description:   (200 mg)
MSDS SDS
Supplier:  BeanTown Chemical
Description:   CAS: 464-48-2; EC No: 207-354-7; MDL No: MFCD00064148; RTECS: EX1250000 UN No: UN2717; Haz Class: 4.1; Packing Group: III Crystalline; Molecular Formula: C10H16O; MW: 152.24 Boiling Point: 204°; Flash point: 65°C (149°F) Density (g/mL): 0.99; Optical Rotation: [α]20/D -43°, c = 10 in ethanol
MSDS SDS
Supplier:  BeanTown Chemical
Description:   CAS: 6018-89-9; EC No: 206-761-7; MDL No: MFCD00066973; RTECS: QR6126000 UN No: UN3077; Haz Class: 9; Packing Group: III Crystalline; Linear Formula: Ni(OCOCH3)2·4H2O; MW: 248.84 Density (g/mL): 1.798
MSDS SDS
Supplier:  BeanTown Chemical
Description:   CAS: 7446-70-0; EC No: 231-208-1; MDL No: MFCD00003422; RTECS: BD0525000 UN No: UN1726; Haz Class: 8; Packing Group: II Granular; Molecular Formula: AlCl3; MW: 133.34 Melting Point: 190° Moisture Sensitive
MSDS SDS
Catalog Number: (10072-974)

Supplier:  Prosci
Description:   NAP-2 is a CXC chemokine that can signal through the CXCR1 and CXCR2 receptors. It is produced in leukocytes by enzymatic processing of a precursor called platelet basic protein (PBP). NAP-2 chemoattracts and activates neutrophils. Recombinant human NAP-2 protein is a 7.6 kDa protein containing 70 amino acid residues including the four highly conserved cysteine residues present in CXC chemokines, and also including the ELR motif common to CXC chemokines that bind to CXCR1 and CXCR2.
Supplier:  Promega Corporation
Description:   EDTA, Disodium Salt, Molecular Biology Grade, is a chelator of divalent metal cations.
MSDS SDS
Supplier:  Sino Biological
Description:   A DNA sequence encoding the F3 (XP_005542723.1) (Met1-Glu252) was expressed with a polyhistidine tag at the C-terminus.
Catalog Number: (103284-138)

Supplier:  Novus Biologicals
Description:   The RASA3 Antibody from Novus Biologicals is a rabbit polyclonal antibody to RASA3. This antibody reacts with human. The RASA3 Antibody has been validated for the following applications: Immunohistochemistry, Immunohistochemistry-Paraffin.
Catalog Number: (103260-366)

Supplier:  Novus Biologicals
Description:   The P4HA3 Antibody from Novus Biologicals is a rabbit polyclonal antibody to P4HA3. This antibody reacts with human. The P4HA3 Antibody has been validated for the following applications: Immunohistochemistry, Immunohistochemistry-Paraffin.
Catalog Number: (103275-306)

Supplier:  Novus Biologicals
Description:   The RTN3 Antibody from Novus Biologicals is a rabbit polyclonal antibody to RTN3. This antibody reacts with human. The RTN3 Antibody has been validated for the following applications: Immunohistochemistry, Immunohistochemistry-Paraffin.

Supplier:  Bioss
Description:   Synaptotagmins are a large family of synaptic vesicle type III integral membrane proteins that function as regulators of both exocytosis and endocytosis and are involved in neurotransmitter secretion from small secretory vesicles. Synaptotagmin XI, also known as SYT11 (Synaptotagmin-11), is a 431 amino acid protein that localizes to the membrane and is expressed ubiquitously with highest expression in brain and lung. Like other Synaptotagmin proteins, Synaptotagmin XI is involved in the calcium-dependent exocytosis of secretory vesicles and is thought to act as a calcium sensor during vesicular trafficking. Synaptotagmin XI contains two C2 domains through which it can bind either three calcium ions or the zinc-finger protein Parkin (a juvenile Parkinson’s disease gene product), the latter of which causes the polyubiquitination and subsequent degradation of Synaptotagmin XI by the proteasome complex. Defects in the gene encoding Synaptotagmin XI are implicated in a number of neurological disorders, including schizophrenia and Parkinson’s disease.
Catalog Number: (103259-116)

Supplier:  Novus Biologicals
Description:   The PLA2G3 Antibody from Novus Biologicals is a rabbit polyclonal antibody to PLA2G3. This antibody reacts with human. The PLA2G3 Antibody has been validated for the following applications: Western Blot, Immunohistochemistry, Immunohistochemistry-Paraffin.
Inquire for Price
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 call 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 call 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
-Additional Documentation May be needed to purchase this item. A VWR representative will contact you if needed.
This product has been blocked by your organization. Please contact your purchasing department for more information.
The original product is no longer available. The replacement shown is available.
This product is no longer available. Alternatives may be available by searching with the VWR Catalog Number listed above. If you need further assistance, please call VWR Customer Service at 1-800-932-5000.
6,321 - 6,336  of 8,801