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2-Bromo-3,6-dimethoxybenzoic+acid
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2-Bromo-3,6-dimethoxybenzoic+acid
Supplier:
AMBEED, INC
Description:
1-Boc-5,6-dihydro-2H-pyridine-3-boronic acid pinacol ester 97%
Catalog Number:
(101849-826)
Supplier:
Matrix Scientific
Description:
Matrix Scientific Part Number: 040598-500MG , MDL Number: MFCD12028306
Supplier:
THERMO FISHER SCIENTIFIC CHEMICALS
Description:
Amphotericin B 85%
Supplier:
Thermo Scientific Chemicals
Description:
MDL: MFCD00008436
Beilstein Registry No.: 2043574
Supplier:
BeanTown Chemical
Description:
CAS: 111-62-6; EC No: 203-889-5; MDL No: MFCD00009579; RTECS: RG3715000
Liquid; Molecular Formula: C20H38O2; MW: 310.51
Melting Point: -32°; Boiling Point: 205-208°; Flash point: <gt/>110°C (<gt/>230°F)
Density (g/mL): 0.87; Refractive Index: 1.451
Light Sensitive
Catalog Number:
(77621-630)
Supplier:
AMBEED, INC
Description:
(S)-5-Benzyl-18-(2,5-dioxo-2,5-dihydro-1H-pyrrol-1-yl)-4,7,10,13-tetraoxo-3,6,9,12-tetraazaoctadecan-1-oic acid ≥98%
Supplier:
PeproTech, Inc.
Description:
SCF is a hematopoietic growth factor that exerts its activity by signaling through the c-Kit receptor. SCF and c-Kit are essential for the survival, proliferation and differentiation of hematopoietic cells committed to the melanocyte and germ cell lineages. Human SCF manifests low activity on murine cells, while murine and rat SCF are fully active on human cells. The human SCF gene encodes for a 273 amino acid transmembrane protein, which contains a 25 amino acid N-terminal signal sequence, a 189 amino acid extracellular domain, a 23 amino acid transmembrane domain, and a 36 amino acid cytoplasmic domain. The secreted soluble form of SCF is generated by proteolytic processing of the membrane anchored precursor. Recombinant Human SCF is an 18.4 kDa polypeptide containing 165 amino acid residues, which corresponds to the sequence of the secreted soluble form of SCF.
Supplier:
Matrix Scientific
Description:
Matrix Scientific Part Number: 050993-500MG , MDL Number: MFCD13561363
Supplier:
TCI America
Description:
CAS Number: 14025-21-9
MDL Number: MFCD00135187 Molecular Formula: C10H16N2O8 Molecular Weight: 399.57 Purity/Analysis Method: >98.0% (T) Form: Crystal
Catalog Number:
(76068-644)
Supplier:
Prosci
Description:
For WB starting dilution is: 1:2000 For IHC-P starting dilution is: 1:50~100
Supplier:
PeproTech, Inc.
Description:
SCF is a hematopoietic growth factor that exerts its activity by signaling through the c-Kit receptor. SCF and c-Kit are essential for the survival, proliferation and differentiation of hematopoietic cells committed to the melanocyte and germ cell lineages. Human SCF manifests low activity on murine cells, while murine and rat SCF are fully active on human cells. The human SCF gene encodes for a 273 amino acid transmembrane protein, which contains a 25 amino acid N-terminal signal sequence, a 189 amino acid extracellular domain, a 23 amino acid transmembrane domain, and a 36 amino acid cytoplasmic domain. The secreted soluble form of SCF is generated by proteolytic processing of the membrane anchored precursor. Recombinant Rat SCF is an 18.4 kDa polypeptide containing 165 amino acid residues, which corresponds to the sequence of the secreted soluble form of SCF.
Catalog Number:
(89161-316)
Supplier:
Enzo Life Sciences
Description:
Peptide tyrosine tyrosine (PYY) is a 36 amino acid peptide, originally isolated from porcine gut, which exhibits striking sequence homology with members of the pancreatic polypeptide family, including neuropeptide tyrosine (NPY). The peptide is localised to enteroglucagon-containing (L/EG) and pancreatic (A) cells in many mammalian and nonmammalian species. PYY gene expression is upregulated by various growth factors, including growth hormone and insulin-like growth factor-1 and the physiological effects of PYY are mediated by G-protein (Gαi2) coupled Y-type receptors (‘Y2 receptors of a PYY-preferring subtype’). Various actions have been reported for PYY, including the inhibition of upper intestinal and exocrine pancreatic secretion, small intestinal water flux and as the mediator for the fat-induced ileal brake. The infusion of normal post-prandial concentrations of PYY[3-36] into human volunteers has been shown to significantly decrease appetite and reduce food intake, possibly via Y2R in the arcuate nucleus. This work stimulated a great deal of research activity showing that the truncated form of PYY reduced food intake in normal and obese humans and in rodents. Recently, the actions of PYY[3-36] and GLP-1[7-36] have been shown to inhibit food intake additively in humans and rats. Immunohistochemical studies on mice have shown that PYY is the earliest detectable peptide in both pancreatic islets and colonic endocrine cells, which suggest that PYY may be a useful marker for endocrine progenitor cells.
Supplier:
ALADDIN SCIENTIFIC
Description:
Alendronate acid is an inhibitor of FDPS. It is a bisphosphonate that inhibits osteoclast-mediated bone resorption. Unlike pyrophosphate, the endogenous regulator of bone turnover to which it is chemically related, alendronate specifically inhibits osteoclastic osteoclastic bone resorption, having no effect on mineralization of bone newly formed by osteoblasts.An inhibitor of FDPS
Catalog Number:
(101789-848)
Supplier:
Matrix Scientific
Description:
MF=C14H9F5O3S MW=352.28 Cas=4455-09-8 MDL=MFCD06248628 25G
Catalog Number:
(76071-016)
Supplier:
Prosci
Description:
For WB starting dilution is: 1:1000 For FACS starting dilution is: 1:10~50
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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.
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