Text Search >
4,4\'-Methylenebis(2,6-diethylaniline)
Print…
You Searched For:
21,652 results were found
4,4\'-Methylenebis(2,6-diethylaniline)
Supplier:
DWK Life Sciences (KIMBLE)
Description:
ASTM E438, Type III amber glass protects light-sensitive chemicals.
Catalog Number:
(10484-012)
Supplier:
Bioss
Description:
BRP44 is a 127 amino acid protein belonging to the UPF0041 family. The gene that encodes BRP44 maps to human chromosome 1, which is the largest human chromosome spanning about 260 million base pairs and making up 8% of the human genome. There are about 3,000 genes on chromosome 1, and considering the great number of genes there are also a large number of diseases associated with chromosome 1. Notably, the rare aging disease Hutchinson-Gilford progeria is associated with the LMNA gene which encodes lamin A. When defective, the LMNA gene product can build up in the nucleus and cause characteristic nuclear blebs. The mechanism of rapidly enhanced aging is unclear and is a topic of continuing exploration. The MUTYH gene is located on chromosome 1 and is partially responsible for familial adenomatous polyposis. Stickler syndrome, Parkinsons, Gaucher disease and Usher syndrome are also associated with chromosome 1. A breakpoint has been identified in 1q which disrupts the DISC1 gene and is linked to schizophrenia. Aberrations in chromosome 1 are found in a variety of cancers including head and neck cancer, malignant melanoma and multiple myeloma.
Supplier:
Justrite
Description:
These Gas Cylinder Barricade Racks provide safety when moving and storing of gas cylinders.
Catalog Number:
(10484-354)
Supplier:
Bioss
Description:
BRP44L, also known as HSPC040 or CGI-129, is a 109 amino acid mitochondrial protein belonging to the UPF0041 family. The gene that encodes BRP44L maps to human chromosome 6. Making up nearly 6% of the human genome, chromosome 6 contains around 1,200 genes within 170 million base pairs of sequence. Deletion of a portion of the q arm of chromosome 6 is associated with early onset intestinal cancer suggesting the presence of a cancer susceptibility locus. Porphyria cutanea tarda is associated with chromosome 6 through the HFE gene which, when mutated, predisposes an individual to developing this porphyria. Notably, the PARK2 gene, which is associated with Parkinson's disease, and the genes encoding the major histocompatiblity complex proteins, which are key molecular components of the immune system and determine predisposition to rheumatic diseases, are also located on chromosome 6. Stickler syndrome, 21-hydroxylase deficiency and maple syrup urine disease are also associated with genes on chromosome 6. A bipolar disorder susceptibility locus has been identified on the q arm of chromosome 6.
Catalog Number:
(10484-336)
Supplier:
Bioss
Description:
BRP44 is a 127 amino acid protein belonging to the UPF0041 family. The gene that encodes BRP44 maps to human chromosome 1, which is the largest human chromosome spanning about 260 million base pairs and making up 8% of the human genome. There are about 3,000 genes on chromosome 1, and considering the great number of genes there are also a large number of diseases associated with chromosome 1. Notably, the rare aging disease Hutchinson-Gilford progeria is associated with the LMNA gene which encodes lamin A. When defective, the LMNA gene product can build up in the nucleus and cause characteristic nuclear blebs. The mechanism of rapidly enhanced aging is unclear and is a topic of continuing exploration. The MUTYH gene is located on chromosome 1 and is partially responsible for familial adenomatous polyposis. Stickler syndrome, Parkinsons, Gaucher disease and Usher syndrome are also associated with chromosome 1. A breakpoint has been identified in 1q which disrupts the DISC1 gene and is linked to schizophrenia. Aberrations in chromosome 1 are found in a variety of cancers including head and neck cancer, malignant melanoma and multiple myeloma.
Catalog Number:
(80066-010)
Supplier:
Chemglass
Description:
Adapters have a #7 Chem-Thread at the top for vacuum tight seal of plain stem thermometers or any other tube having an O.D. between 4 and 7 mm.
Catalog Number:
(10484-016)
Supplier:
Bioss
Description:
BRP44 is a 127 amino acid protein belonging to the UPF0041 family. The gene that encodes BRP44 maps to human chromosome 1, which is the largest human chromosome spanning about 260 million base pairs and making up 8% of the human genome. There are about 3,000 genes on chromosome 1, and considering the great number of genes there are also a large number of diseases associated with chromosome 1. Notably, the rare aging disease Hutchinson-Gilford progeria is associated with the LMNA gene which encodes lamin A. When defective, the LMNA gene product can build up in the nucleus and cause characteristic nuclear blebs. The mechanism of rapidly enhanced aging is unclear and is a topic of continuing exploration. The MUTYH gene is located on chromosome 1 and is partially responsible for familial adenomatous polyposis. Stickler syndrome, Parkinsons, Gaucher disease and Usher syndrome are also associated with chromosome 1. A breakpoint has been identified in 1q which disrupts the DISC1 gene and is linked to schizophrenia. Aberrations in chromosome 1 are found in a variety of cancers including head and neck cancer, malignant melanoma and multiple myeloma.
Supplier:
TCI America
Description:
CAS Number: 1189-71-5
MDL Number: MFCD00011608 Molecular Formula: CClNO3S Molecular Weight: 141.53 Purity/Analysis Method: >98.0% (GC) Form: Clear Liquid Boiling point (°C): 107 Melting point (°C): -80 Flash Point (°C): 110 Specific Gravity (20/20): 1.64 Storage Temperature: 0-10°C
Supplier:
Vileda Professional - FHP
Description:
FHP bucket and wringer combos are designed to meet the demanding requirements of the most sanitary environments.
Catalog Number:
(89277-950)
Supplier:
Genetex
Description:
Rabbit Polyclonal to Human Protein Phosphatase MGC1136
Catalog Number:
(MSPP-PAG277HU1)
Supplier:
CLOUD-CLONE CORP MS
Description:
Polyclonal antibody to Proteasome 26S Subunit, ATPase 2 (PSMC2), derived from recombinant PSMC2(Met1~Asn433), is reactive with Human/Mouse/Rat.
Catalog Number:
(80088-304)
Supplier:
Abgent
Description:
Primary Rabbit Anti-CCL19 (C-term) Reacts with Human
Catalog Number:
(89517-110)
Supplier:
Abgent
Description:
Western Blot: 1:1000
Catalog Number:
(82004-778)
Supplier:
Cardinal Health
Description:
This single-ply gauze is 100% mesh.
Catalog Number:
(10058-726)
Supplier:
Restek
Description:
This nitrogen gas generators turn compressed air into ultra-pure nitrogen (up to 99.5%).
Catalog Number:
(80511-204)
Supplier:
MilliporeSigma
Description:
An amyloidophylic dye that specifically stains stacked β sheet aggregates.
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
 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
-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.
|
|||||||||
List View
