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Image Unavailable-EM8.40124.0100

Span® 85 for synthesis, Sigma-Aldrich®

Description: Span® 85 for synthesis, Sigma-Aldrich®
Catalog Number: EM8.40124.0100
Supplier: MilliporeSigma

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Image Unavailable-TCS0064-500G

Span® 85

Description: CAS Number: 26266-58-0
MDL Number: MFCD00133820
Form: Clear Liquid
Color: Yellow
Melting point (°C): -23
Flash Point (°C): 253
Specific Gravity (20/20): 0.95
Catalog Number: TCS0064-500G
Supplier: TCI America

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Image Unavailable-76879-612

Sorbitan trioleate Saponification Value 165-180

Description: Sorbitan trioleate Saponification Value 165-180
Catalog Number: 76879-612
Supplier: Ambeed

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Image Unavailable-700011-086

Sorbitan trioleate

Description: Sorbitan Trioleate is used in lubricants and rust preventive oils for its corrosion inhibition property. Ungraded products supplied by Spectrum are indicative of a grade suitable for general industrial use or research purposes and typically are not suitable for human consumption or therapeutic use.
Catalog Number: 700011-086
Supplier: Spectrum Chemicals

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Image Unavailable-77436-808

Anti-LRP1 Rabbit Polyclonal Antibody

Description: Low density lipoprotein receptor-related protein (also known as low density LRP, LRP1, alpha-2-macroglobulin receptor or Apolipoprotein E receptor) is an endocytotic receptor that is involved both in endocytosis and in phagocytosis of apoptotic cells. It is required for early embryonic development, is involved in cellular lipid homeostasis, and may play a role in APP metabolism, kinase-dependent intracellular signalling, neuronal calcium signalling and neurotransmission. Low density LRP also plays a role in the plasma clearance of chylomicron remnants and activated LRPAP1 (alpha-2-macroglobulin), and is involved in the local metabolism of complexes of plasminogen activators and their endogenous ligands. Low density LPR is postulated to be one of the major players in host resistance to HIV. The precursor low density LRP molecule is cleaved post-translationally to form a 85 kDa membrane-spanning subunit (LRP-85) and a 515 kDa large extracellular domain (LRP-515), which remains non-covalently associated with LRP-85. Following cleavage, the intracellular domain (LPRICD) is present in both the cytoplasm and the nucleus.
Catalog Number: 77436-808
Supplier: Bioss
Image Unavailable-10310-546

Anti-C1orf85 Rabbit Polyclonal Antibody (FITC (Fluorescein Isothiocyanate))

Description: C1orf85, also known as Lysosomal protein NCU-G1, is a 406 amino acid single-pass membrane protein that is highly glycosylated on its amino-terminal end. Transcription of the gene encoding C1orf85 is activated by TFEB, a transcription factor that specifically recognizes and binds E-box sequences. There are two isoforms of C1orf85 that are produced as a result of alternative splicing events. The C1orf85 maps to human chromosome 1, 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.
Catalog Number: 10310-546
Supplier: Bioss
Image Unavailable-10316-388

Anti-C1orf85 Rabbit Polyclonal Antibody (Cy3®)

Description: C1orf85, also known as Lysosomal protein NCU-G1, is a 406 amino acid single-pass membrane protein that is highly glycosylated on its amino-terminal end. Transcription of the gene encoding C1orf85 is activated by TFEB, a transcription factor that specifically recognizes and binds E-box sequences. There are two isoforms of C1orf85 that are produced as a result of alternative splicing events. The C1orf85 maps to human chromosome 1, 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.
Catalog Number: 10316-388
Supplier: Bioss
Image Unavailable-10316-392

Anti-C1orf85 Rabbit Polyclonal Antibody (Cy7®)

Description: C1orf85, also known as Lysosomal protein NCU-G1, is a 406 amino acid single-pass membrane protein that is highly glycosylated on its amino-terminal end. Transcription of the gene encoding C1orf85 is activated by TFEB, a transcription factor that specifically recognizes and binds E-box sequences. There are two isoforms of C1orf85 that are produced as a result of alternative splicing events. The C1orf85 maps to human chromosome 1, 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.
Catalog Number: 10316-392
Supplier: Bioss
Image Unavailable-10316-390

Anti-C1orf85 Rabbit Polyclonal Antibody (Cy5®)

Description: C1orf85, also known as Lysosomal protein NCU-G1, is a 406 amino acid single-pass membrane protein that is highly glycosylated on its amino-terminal end. Transcription of the gene encoding C1orf85 is activated by TFEB, a transcription factor that specifically recognizes and binds E-box sequences. There are two isoforms of C1orf85 that are produced as a result of alternative splicing events. The C1orf85 maps to human chromosome 1, 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.
Catalog Number: 10316-390
Supplier: Bioss
Image Unavailable-10310-548

Anti-C1orf85 Rabbit Polyclonal Antibody (HRP (Horseradish Peroxidase))

Description: C1orf85, also known as Lysosomal protein NCU-G1, is a 406 amino acid single-pass membrane protein that is highly glycosylated on its amino-terminal end. Transcription of the gene encoding C1orf85 is activated by TFEB, a transcription factor that specifically recognizes and binds E-box sequences. There are two isoforms of C1orf85 that are produced as a result of alternative splicing events. The C1orf85 maps to human chromosome 1, 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.
Catalog Number: 10310-548
Supplier: Bioss
Product Image-77889-470

VWR® Erlenmeyer Shaker Flasks with Plain Bottom, Sterile

Description: <p><span style="color:black">Erlenmeyer shaker flasks provide excellent optical clarity and mechanical strength. They are ideal for suspension cell culture applications, storage, mixing and other purposes.</span></p>
Catalog Number: 77889-470
Supplier: VWR International

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Image Unavailable-EM8.40119.0100

Span® 20 for synthesis, Sigma-Aldrich®

Description: Span® 20 for synthesis, Sigma-Aldrich®
Catalog Number: EM8.40119.0100
Supplier: MilliporeSigma

SDS Certificates


Image Unavailable-EM8.40123.0100

Span® 80 for synthesis, Sigma-Aldrich®

Description: SPan(R) 80, CAS no : 1338-43-8, Synonyms Sorbitan monooleate, (Z)-Sorbitan mono-9-octadecenoate, for synthesis, 1l
Catalog Number: EM8.40123.0100
Supplier: MilliporeSigma

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Image Unavailable-EM8.40122.0100

Span® 65, Span® for synthesis, Sigma-Aldrich®

Catalog Number: EM8.40122.0100
Supplier: MilliporeSigma

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Image Unavailable-BT133545-250G

Span® 40

Description: CAS: 26266-57-9; EC No: 247-568-8; MDL No: MFCD00080946; RTECS: WG2932900 Crystalline; Molecular Formula: C22H42O6; MW: 402.57 Melting Point: 46-47°; Flash point: 113°C (235°F)
Catalog Number: BT133545-250G
Supplier: BeanTown Chemical

SDS


Image Unavailable-TCS0061-500G

Span® 40

Description: CAS Number: 26266-57-9
MDL Number: MFCD00080946
Form: Pellet
Color: Pale Yellow
Melting point (°C): 47
Flash Point (°C): 113
Catalog Number: TCS0061-500G
Supplier: TCI America

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