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2-(2,6-Dimethylphenylcarbamoyl)benzoic+acid
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2-(2,6-Dimethylphenylcarbamoyl)benzoic+acid
Catalog Number:
(10251-542)
Supplier:
Bioss
Description:
Myotubularin-related protein 14 (MTMR14), also known as Jumpy, is a myotubularin-related phosphoinositol-3-phosphate (PI3P) phosphatase (1). Mutations in the MTMR14 gene have been associated with centronuclear myopathy (1). MTMR14 deficiency in mice leads to altered calcium homeostasis and muscle disorders (2). MTMR14 has also been shown to play a role in autophagy, a process that is highly regulated by phosphatidylinositides through the type III PI3K, Vps34 (3). MTMR14 was localized to autophagic isolation membranes and early autophagosomes (3). In these studies, MTMR14 inhibited autophagy and mutations of MTMR14 associated with centronuclear myopathy were also defective in autophagy inhibition. In zebrafish, MTMR14 knockdown was shown to increase the number of autophagosomes, suggesting that its activity is associated with an inhibition of autophagy (4).
Catalog Number:
(10250-776)
Supplier:
Bioss
Description:
Myotubularin-related protein 14 (MTMR14), also known as Jumpy, is a myotubularin-related phosphoinositol-3-phosphate (PI3P) phosphatase (1). Mutations in the MTMR14 gene have been associated with centronuclear myopathy (1). MTMR14 deficiency in mice leads to altered calcium homeostasis and muscle disorders (2). MTMR14 has also been shown to play a role in autophagy, a process that is highly regulated by phosphatidylinositides through the type III PI3K, Vps34 (3). MTMR14 was localized to autophagic isolation membranes and early autophagosomes (3). In these studies, MTMR14 inhibited autophagy and mutations of MTMR14 associated with centronuclear myopathy were also defective in autophagy inhibition. In zebrafish, MTMR14 knockdown was shown to increase the number of autophagosomes, suggesting that its activity is associated with an inhibition of autophagy (4).
Catalog Number:
(10293-892)
Supplier:
Bioss
Description:
GALK2 is important in the first step of the galactose metabolism pathway. GALK1, which belongs to the GHMP kinase family of proteins, is a crucial enzyme for galactose metabolism, specifically converting ?d-galactose to galactose 1-phosphate. Defects in the gene encoding GALK1 can cause galactosemia II, an autosomal recessive disorder characterized by congenital cataracts during infancy, often within the first two weeks of life. In the adult population, galactosemia II can cause presenile cataracts that are secondary to accumulation of galactitol in the lens of the eye. A second gene, GALK2, encodes an enzyme with greater activity against GalNAc than galactose. GALK2 has been implicated in the salvage pathway for the reutilization of free GalNAc derived from the degradation of complex carbohydrates.
Catalog Number:
(75841-350)
Supplier:
BIOGEMS INTERNATIONAL INC.
Description:
MOPC-21 is a Mousemyeloma protein from the Ig family. It can be used as an Isotype Control for MouseIgG1 antibodies.
Catalog Number:
(RL202-4107)
Supplier:
Rockland Immunochemical
Description:
Secondary Rabbit Anti-IgM mu chain Reacts with Cat (Feline)
Catalog Number:
(RL102-4107)
Supplier:
Rockland Immunochemical
Description:
Secondary Rabbit Anti-IgM mu chain Reacts with Cat (Feline)
Catalog Number:
(RL213-4107)
Supplier:
Rockland Immunochemical
Description:
Secondary Rabbit Anti-IgM mu chain Reacts with Sheep (Ovine)
Catalog Number:
(76067-912)
Supplier:
Prosci
Description:
For WB starting dilution is: 1:1000
Catalog Number:
(75931-478)
Supplier:
Rockland Immunochemical
Description:
Rat IgG F(ab')2 Fragment
Catalog Number:
(10298-820)
Supplier:
Bioss
Description:
This gene encodes two of three subunit types of the membrane-bound enzyme N-acetylglucosamine-1-phosphotransferase, a heterohexameric complex composed of two alpha, two beta, and two gamma subunits. The encoded protein is proteolytically cleaved at the Lys928-Asp929 bond to yield mature alpha and beta polypeptides while the gamma subunits are the product of a distinct gene (GeneID 84572). In the Golgi apparatus, the heterohexameric complex catalyzes the first step in the synthesis of mannose 6-phosphate recognition markers on certain oligosaccharides of newly synthesized lysosomal enzymes. These recognition markers are essential for appropriate trafficking of lysosomal enzymes. Mutations in this gene have been associated with both mucolipidosis II and mucolipidosis IIIA.[provided by RefSeq, May 2010].
Catalog Number:
(76068-274)
Supplier:
Prosci
Description:
For WB starting dilution is: 1:1000 For FACS starting dilution is: 1:10~50
Catalog Number:
(RLB310)
Supplier:
Rockland Immunochemical
Description:
The whole sera are prepared from normal sera by a multi-step process that includes delipidation and selective precipitation
Catalog Number:
(75843-384)
Supplier:
BIOGEMS INTERNATIONAL INC.
Description:
The C1.18.4 monoclonal antibody is used as an Isotype Control for MouseIgG2a antibodies. It has unknown specificity and occurred spontaneously in a C3H mouse.
Catalog Number:
(75843-380)
Supplier:
BIOGEMS INTERNATIONAL INC.
Description:
The C1.18.4 monoclonal antibody is used as an Isotype Control for MouseIgG2a antibodies. It has unknown specificity and occurred spontaneously in a C3H mouse.
Catalog Number:
(75841-346)
Supplier:
BIOGEMS INTERNATIONAL INC.
Description:
MOPC-21 is a Mousemyeloma protein from the Ig family. It can be used as an Isotype Control for MouseIgG1 antibodies.
Supplier:
International Products
Description:
Powerful aqueous cleaning concentrate designed for both industrial and laboratory machine-based washing systems
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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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