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Catalog Number: (10492-522)
Supplier: Bioss
Description: Chromosome 1 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. The FAM76A gene product has been provisionally designated FAM76A pending further characterization.


Catalog Number: (10492-516)
Supplier: Bioss
Description: Chromosome 1 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. The FAM76A gene product has been provisionally designated FAM76A pending further characterization.


Catalog Number: (10492-518)
Supplier: Bioss
Description: Chromosome 1 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. The FAM76A gene product has been provisionally designated FAM76A pending further characterization.


Catalog Number: (10494-058)
Supplier: Bioss
Description: Chromosome 1 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. The FAM78B gene product has been provisionally designated FAM78B pending further characterization.


Supplier: TCI America
Description: CAS Number: 17814-85-6
MDL Number: MFCD00011906
Molecular Formula: C23H24BrO2P
Molecular Weight: 443.32
Purity/Analysis Method: >98.0% (HPLC,T)
Form: Crystal
Melting point (°C): 207
Catalog Number: (TCD0977-025G)
Supplier: TCI America
Description: CAS Number: 2561-85-5
MDL Number: MFCD00022610
Molecular Formula: C16H28O3
Molecular Weight: 268.40
Purity/Analysis Method: >95.0% (GC,T)
Form: Crystal
Melting point (°C): 73

Catalog Number: (TCD1029-025G)
Supplier: TCI America
Description: [for Ti Analysis]
CAS Number: 1251-85-0
MDL Number: MFCD00149122
Molecular Formula: C23H24N4O2
Molecular Weight: 388.47
Purity/Analysis Method: >98.0% (T)
Form: Crystal

Supplier: TCI America
Description: CAS Number: 2439-85-2
MDL Number: MFCD00005888
Molecular Formula: C8H4BrNO2
Molecular Weight: 226.03
Purity/Analysis Method: >95.0% (T)
Form: Crystal
Melting point (°C): 207
Catalog Number: (89416-808)
Supplier: Prosci
Description: JPH3 Antibody: Junctional complexes between the plasma membrane (PM) and endoplasmic/sarcoplasmic reticulum (ER/SR) are a common feature of all excitable cell types and mediate cross talk between cell surface and intracellular ion channels. Junctophilins (JPs) are important components of the junctional complexes. JPs are composed of a carboxy-terminal hydrophobic segment spanning the ER/SR membrane and a remaining cytoplasmic domain that shows specific affinity for the PM. Four JPs have been identified as tissue-specific subtypes derived from different genes: JPH1 is expressed in skeletal muscle, JPH2 is detected throughout all muscle cell types, and JPH3 and JPH4 are predominantly expressed in the brain. In the CNS, both JPH3 and JPH4 are expressed throughout neural sites and contribute to the subsurface cistern formation in neurons. Mice lacking both JPH3 and JPH4 subtypes exhibit serious symptoms such as impaired learning and memory and are accompanied by abnormal nervous functions. A repeat expansion in JPH3 is associated with Huntington disease-like 2. At least two isoforms of JPH3 are known to exist.


Supplier: Abcam
Description: Rabbit monoclonal [EPR22344-85] to BTC - BSA and Azide free (Capture).

New Product

Supplier: TCI America
Description: CAS Number: 513-85-9
MDL Number: MFCD00004523
Molecular Formula: C4H10O2
Molecular Weight: 90.12
Purity/Analysis Method: >97.0% (GC)
Form: Clear Liquid
Boiling point (°C): 182
Flash Point (°C): 85
Specific Gravity (20/20): 0.99
Supplier: TCI America
Description: CAS Number: 85-56-3
MDL Number: MFCD00002474
Molecular Formula: C14H9ClO3
Molecular Weight: 260.67
Purity/Analysis Method: >98.0% (GC,T)
Form: Crystal
Melting point (°C): 151

SDS

Supplier: Thermo Scientific Chemicals
Description: Orthophosphoric acid ≥85% in aqueous solution
Supplier: TCI America
Description: CAS Number: 92-85-3
MDL Number: MFCD00005065
Molecular Formula: C12H8S2
Molecular Weight: 216.32
Purity/Analysis Method: >98.0% (GC)
Form: Crystal
Color: White
Melting point (°C): 156
Supplier: TCI America
Description: CAS Number: 40611-85-6
MDL Number: MFCD00191668
Molecular Formula: C8H11NO2
Molecular Weight: 153.18
Purity/Analysis Method: >97.0% (GC)
Form: Crystal
Boiling point (°C): 104
Melting point (°C): 43
Supplier: Thermo Scientific Chemicals
Description: Trifluoroacetamidine tech. 85%, Technical Grade
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