Print…

You Searched For: Magnesium+ethanolate


2,412  results were found

Refine Results Sort by
SearchResultCount:"2412"

Sort Results

List View Easy View

Rate These Search Results

Product Image-10108-634

Anti-ADH6 Rabbit Polyclonal Antibody

Catalog Number: (10108-634)
Supplier: Prosci
Description: ADH6 is class V alcohol dehydrogenase, which is a member of the alcohol dehydrogenase family. Members of this family metabolize a wide variety of substrates, including ethanol, retinol, other aliphatic alcohols, hydroxysteroids, and lipid peroxidation products.
Product Image-CA101444-748

Taq 5X Master Mix, New England Biolabs

Catalog Number: (CA101444-748)
Supplier: New England Biolabs (NEB)
Description: Taq 5X Master Mix is an optimized ready-to-use solution containing Taq DNA Polymerase, dNTPs, MgCl2, KCl and stabilizers
Product Image-470343-470

Innovating Science® DNA Extraction Lab Activity

Supplier: Ward's Science
Description: Learn the history of the discovery of DNA and DNA structure, the nature of genetic inheritance, and the tole of DNA and proteins in genetic expression.

Product Image-89417-830

Anti-ATP2C2 Rabbit Polyclonal Antibody

Catalog Number: (89417-830)
Supplier: Prosci
Description: ATP2C2 Antibody: ATP2C2, also known as secretory pathway Ca2+/Mn2+-ATPase (SPCA) 2, belongs to the family of P-type cation transport ATPases. This magnesium-dependent enzyme catalyzes the hydrolysis of ATP coupled with the transport of the calcium from the cytosol to the Golgi lumen. Defects in the related gene ATP2C1 cause Hailey-Hailey disease, for which ATP2C2 does not compensate, suggesting that ATP2C2 plays other physiological roles. Unlike ATP2C1, ATP2C2 has a much more restricted expression pattern and displays a higher maximal turnover rate for overall Ca2+-ATPase reaction and a lower apparent affinity for cytosolic Ca2+ activation of phosphorylation. Overexpression of ATP2C2 in mammary tumors result a Ca2+ influx via the store-operated Ca2+ channel ORAI1 and independent of the STIM1 and STIM2 sensors.
Image Unavailable-10496-318

Anti-TSSK6 Rabbit Polyclonal Antibody (Cy5®)

Catalog Number: (10496-318)
Supplier: Bioss
Description: The phosphorylation and dephosphorylation of proteins on serine and threonine residues is an essential means of regulating a broad range of cellular functions in eukaryotes, including cell division, homeostasis and apoptosis. A group of proteins that are intimately involved in this process are the serine/threonine (Ser/Thr) protein kinases. TSSK 6 (testis-specific serine kinase 6), also known as SSTK, TSSK4, FKSG82 or CT72, is a 273 amino acid protein that contains one protein kinase domain and belongs to the Ser/Thr protein kinase family. Highly expressed in testis with lower expression in ovary, colon, thymus, small intestine and spleen, TSSK 6 catalyzes the ATP-dependent phosphorylation of proteins involved in sperm production and chromatin remodeling. TSSK 6 uses magnesium as a cofactor and is thought to be required for proper sperm development and function, as well as DNA condensation events. Defects in the gene encoding TSSK 6 are associated with male infertility characterized by low sperm count and decreased sperm motility.
Image Unavailable-10496-320

Anti-TSSK6 Rabbit Polyclonal Antibody (Cy5.5®)

Catalog Number: (10496-320)
Supplier: Bioss
Description: The phosphorylation and dephosphorylation of proteins on serine and threonine residues is an essential means of regulating a broad range of cellular functions in eukaryotes, including cell division, homeostasis and apoptosis. A group of proteins that are intimately involved in this process are the serine/threonine (Ser/Thr) protein kinases. TSSK 6 (testis-specific serine kinase 6), also known as SSTK, TSSK4, FKSG82 or CT72, is a 273 amino acid protein that contains one protein kinase domain and belongs to the Ser/Thr protein kinase family. Highly expressed in testis with lower expression in ovary, colon, thymus, small intestine and spleen, TSSK 6 catalyzes the ATP-dependent phosphorylation of proteins involved in sperm production and chromatin remodeling. TSSK 6 uses magnesium as a cofactor and is thought to be required for proper sperm development and function, as well as DNA condensation events. Defects in the gene encoding TSSK 6 are associated with male infertility characterized by low sperm count and decreased sperm motility.
Image Unavailable-TCM2624-1G

2-Hydroxyethylmesitylene ≥98.0%

Supplier: TCI America
Description: CAS Number: 6950-92-1
MDL Number: MFCD00020609
Molecular Formula: C11H16O
Molecular Weight: 164.25
Purity/Analysis Method: >98.0% (GC)
Form: Crystal
Boiling point (°C): 152
Melting point (°C): 80

SDS

Image Unavailable-76110-646

Anti-FIGNL1 Rabbit Polyclonal Antibody (Alexa Fluor® 680)

Catalog Number: (76110-646)
Supplier: Bioss
Description: FIGNL1 is a 674 amino acid protein belonging to the AAA ATPase family. FIGNL1 exists as a hexamer that undergoes alternative splicing to produce two isoforms. FIGNL1 utilizes magnesium as a cofactor and is phosphorylated upon DNA damage, probably by ATM or ATR. FIGNL1 is suggested to regulate osteoblast proliferation and differentiation. FIGNL1 is encoded by a gene located on human chromosome 7, which consists about 158 million bases, encodes over 1000 genes and makes up about 5% of the human genome. Chromosome 7 has been linked to Osteogenesis imperfecta, Pendred syndrome, Lissencephaly, Citrullinemia and Shwachman-Diamond syndrome. The deletion of a portion of the q arm of chromosome 7 is associated with Williams-Beuren syndrome, a condition characterized by mild mental retardation, an unusual comfort and friendliness with strangers and an elfin appearance. Deletions of portions of the q arm of chromosome 7 are also seen in a number of myeloid disorders including cases of acute myelogenous leukemia and myelodysplasia.
Product Image-470121-766

Lab 9: Principles of Transpiration

Catalog Number: (470121-766)
Supplier: Edvotek
Description: Applying what was learned in Lab 1, students study the movement of water within the plant, then prepare and study sections of fresh plant stem tissueRequired, but not included: microscope(s), slides and coverslips, ring stands and clamps, 100 W light source, fan, scale or balance, spray bottle, 10 ml pipets, spatulas, razor or scalpel blades, potting soil, petroleum jelly, 50% ethanol, mounting media, and large plastic bags. For 10 student groups.
Image Unavailable-10487-954

Anti-FIGNL1 Rabbit Polyclonal Antibody (Cy3®)

Catalog Number: (10487-954)
Supplier: Bioss
Description: FIGNL1 is a 674 amino acid protein belonging to the AAA ATPase family. FIGNL1 exists as a hexamer that undergoes alternative splicing to produce two isoforms. FIGNL1 utilizes magnesium as a cofactor and is phosphorylated upon DNA damage, probably by ATM or ATR. FIGNL1 is suggested to regulate osteoblast proliferation and differentiation. FIGNL1 is encoded by a gene located on human chromosome 7, which consists about 158 milllion bases, encodes over 1000 genes and makes up about 5% of the human genome. Chromosome 7 has been linked to Osteogenesis imperfecta, Pendred syndrome, Lissencephaly, Citrullinemia and Shwachman-Diamond syndrome. The deletion of a portion of the q arm of chromosome 7 is associated with Williams-Beuren syndrome, a condition characterized by mild mental retardation, an unusual comfort and friendliness with strangers and an elfin appearance. Deletions of portions of the q arm of chromosome 7 are also seen in a number of myeloid disorders including cases of acute myelogenous leukemia and myelodysplasia.
Image Unavailable-10487-964

Anti-FIGNL1 Rabbit Polyclonal Antibody (HRP (Horseradish Peroxidase))

Catalog Number: (10487-964)
Supplier: Bioss
Description: FIGNL1 is a 674 amino acid protein belonging to the AAA ATPase family. FIGNL1 exists as a hexamer that undergoes alternative splicing to produce two isoforms. FIGNL1 utilizes magnesium as a cofactor and is phosphorylated upon DNA damage, probably by ATM or ATR. FIGNL1 is suggested to regulate osteoblast proliferation and differentiation. FIGNL1 is encoded by a gene located on human chromosome 7, which consists about 158 milllion bases, encodes over 1000 genes and makes up about 5% of the human genome. Chromosome 7 has been linked to Osteogenesis imperfecta, Pendred syndrome, Lissencephaly, Citrullinemia and Shwachman-Diamond syndrome. The deletion of a portion of the q arm of chromosome 7 is associated with Williams-Beuren syndrome, a condition characterized by mild mental retardation, an unusual comfort and friendliness with strangers and an elfin appearance. Deletions of portions of the q arm of chromosome 7 are also seen in a number of myeloid disorders including cases of acute myelogenous leukemia and myelodysplasia.
Image Unavailable-SXS-1890

Ethanolamine Single-Component Organic Standard, SPEX CertiPrep

Catalog Number: (SXS-1890)
Supplier: SPEX CERTIPREP LLC
Description: Single-Component organic standards.
Product Image-CA102902-472

MluI-HF, Restriction Enzymes, New England Biolabs

Supplier: New England Biolabs (NEB)
Description: MluI-HF is produced in E. coli from a strain that carries the cloned and modified MluI gene from Micrococcus luteus (IFO 12992)

Image Unavailable-TCH1043-1G

Hexaethylene glycol monobenzyl ether ≥93.0%

Catalog Number: (TCH1043-1G)
Supplier: TCI America
Description: CAS Number: 24342-68-5
MDL Number: MFCD06797107
Molecular Formula: C19H32O7
Molecular Weight: 372.46
Purity/Analysis Method: >93.0% (GC)
Form: Clear Liquid

SDS Certificates


Product Image-CA102902-468

NruI-HF, Restriction Enzymes, New England Biolabs

Supplier: New England Biolabs (NEB)
Description: NruI-HF is produced in E. coli from a strain that carries the cloned and modified NruI gene from Nocardia rubra (ATCC 15906).

Image Unavailable-TCT1997-5G

Tetraethylene glycol monobenzyl ether ≥95.0% (by GC)

Catalog Number: (TCT1997-5G)
Supplier: TCI America
Description: CAS Number: 86259-87-2
MDL Number: MFCD06797175
Molecular Formula: C15H24O5
Molecular Weight: 284.35
Purity/Analysis Method: >95.0% (GC)
Form: Clear Liquid
Color: Very Pale Yellow
Specific Gravity (20/20): 1.10

SDS Certificates


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.
You must log in to order restricted items. We request that you provide the required business documentation to purchase this product for the first time.

To order chemicals, medical devices, or other restricted products please provide identification that includes your business name and shipping address via email CMD_NA@vwr.com or fax 484.881.5997 referencing your VWR account number . Acceptable forms of identification are:

  • issued document with your organization's Federal Tax ID Number
  • Government issued document with your organization's Resale Tax ID Number
  • Any other Government ID that includes the business name and address


VWR will not lift restrictions for residential shipping addresses.

-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 currently unavailable but limited stock may be available in our extended warehouse network. Please call 1-800-932-5000 and a VWR Customer Service Representative will help you.
993 - 1,008 of 2,412
no targeter for Bottom