Ace+Method+Development+Kits
Supplier:
Restek
Description:
Unwashed PUF plugs for both low-volume and high-volume sampling.
Catalog Number:
(10103-642)
Supplier:
Prosci
Description:
The exact function of C12orf49 remains unknown.
Catalog Number:
(10104-092)
Supplier:
Prosci
Description:
The specific function of CCDC38 is not yet known.
Catalog Number:
(10101-726)
Supplier:
Prosci
Description:
PRDM8 may be involved in transcriptional regulation.
Catalog Number:
(10782-646)
Supplier:
Biosensis
Description:
FUNCTION: Nerve growth factor is important for the development and maintenance of the sympathetic and sensory nervous systems. It stimulates division and differentiation of sympathetic and embryonic sensory neurons. SUBUNIT: Homodimer, associated by noncovalent forces. SUBCELLULAR LOCATION: Secreted protein. SIMILARITY: Belongs to the NGF-beta family.
Supplier:
TCI America
Description:
CAS Number: 618-27-9
Molecular Formula: C5H9NO3 Molecular Weight: 131.13 Purity/Analysis Method: >97.0% (T) Form: Crystal Melting point (°C): 241 Specific rotation [a]20/D: -59 deg (C=2, H2O)
Catalog Number:
(10460-950)
Supplier:
Bioss
Description:
Plays a role as a transcriptional repressor during development. May play a role in the control of cell survival. Overexpression of RERE recruits BAX to the nucleus particularly to POD and triggers caspase-3 activation, leading to cell death.
Catalog Number:
(76110-698)
Supplier:
Bioss
Description:
Ligand for members of the frizzled family of seven transmembrane receptors. Probable developmental protein. May be a signaling molecule which affects the development of discrete regions of tissues. Is likely to signal over only few cell diameters (By similarity).
Catalog Number:
(BDH4606-500G)
Supplier:
VWR International
Description:
di-Sodium L(+)-tartrate dihydrate 99.0-101.0% ACS, VWR Chemicals BDH®
Supplier:
Metropolitan Wire
Description:
ESD Cart Covers provide an effective method of controlling electrostatic discharge while portecting cart contents from contamination and moisture
Catalog Number:
(10104-042)
Supplier:
Prosci
Description:
The exact function of IQCF1 is not known.
Catalog Number:
(75835-178)
Supplier:
Restek
Description:
Standard Acetochlor, CAS number: 34256-82-1, Purity: 98%, Concentration: 100 ug/mL, Solvent: methanol, Volume: 1 mL/ampul, Shelf Life: 6 months, Storage: 10 deg C
Supplier:
PeproTech, Inc.
Description:
Human sDLL-4 comprises the extracellular signaling domain of DLL, a member of a structurally-related family of single-pass type I trans-membrane proteins that serve as ligands for Notch receptors. DLL-4 functions to specifically activate the Notch-1 and Notch-4 receptors. The Notch signaling pathway regulates endothelial cell differentiation, proliferation and apoptosis, and is essential for the development, maintenance and remodeling of the vascular system. Targeted deletion of the DLL-4 gene in mice resulted in severe vascular defects and death before birth. Up-regulation of DLL-4 expression has been implicated in the vascular development of certain tumors. The human DLL-4 gene consists of a 503 amino acid extracellular domain with one DSL domain, eight EGF-like repeats, a 21 a.a. transmembrane domain, and a 135 a.a. cytoplasmic domain. Recombinant Human sDLL-4 is a 54.3 kDa glycoprotein containing 498 amino acid residues.
Catalog Number:
(10412-900)
Supplier:
Bioss
Description:
Separase is a cysteine protease that is essential for mitotic progression by separating sister chromatids. Each cell must receive one chromatid of every chromosome, during mitosis. Cohesin plays an important role in cohering sister chromatids during the prophase through anaphase stages of mitosis, making certain that genomic information is replicated accurately. As the cellular division process continues, separase destroys cohesin by means of cleavage, allowing the chromatids to separate and divide with the cell. Separase activity is highly regulated. It not only cleaves cohesin at the onset of anaphase but also cleaves itself, promoting downregulation of separase after anaphase. Should a human cell become an aneuploid (one too many or too few chromatids), the embryo most likely will not survive. Should the embryo survive, it will most likely develop severe birth defects or later develop malignant cancers.
Catalog Number:
(10450-674)
Supplier:
Bioss
Description:
Receptor tyrosine kinase which binds promiscuously GPI-anchored ephrin-A family ligands residing on adjacent cells, leading to contact-dependent bidirectional signaling into neighboring cells. The signaling pathway downstream of the receptor is referred to as forward signaling while the signaling pathway downstream of the ephrin ligand is referred to as reverse signaling. Among GPI-anchored ephrin-A ligands, EFNA5 most probably constitutes the cognate/functional ligand for EPHA5. Functions as an axon guidance molecule during development and may be involved in the development of the retinotectal, entorhino-hippocampal and hippocamposeptal pathways. Together with EFNA5 plays also a role in synaptic plasticity in adult brain through regulation of synaptogenesis. In addition to its function in the nervous system, the interaction of EPHA5 with EFNA5 mediates communication between pancreatic islet cells to regulate glucose-stimulated insulin secretion (By similarity).
Catalog Number:
(10448-594)
Supplier:
Bioss
Description:
CGI-99 is a 244 amino acid protein that localizes to the nucleus, as well as to the cytoplasm, and belongs to the UPF0568 family. Expressed in a variety of tissues with particularly high levels in heart and skeletal muscle, CGI-99 functions as a homodimer that interacts with Ninein and is thought to regulate Ninein function. CGI-99 is overexpressed in brain tumor tissue, suggesting a role in tumor development and metastasis. The gene encoding CGI-99 maps to human chromosome 14, which houses over 700 genes and comprises nearly 3.5% of the human genome. Chromosome 14 encodes the presinilin 1 (PSEN1) gene, which is one of the three key genes associated with the development of Alzheimer's disease (AD). The SERPINA1 gene is also located on chromosome 14 and, when defective, leads to the genetic disorder ?-antitrypsin deficiency, which is characterized by severe lung complications and liver dysfunction.
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