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Span® 85 for synthesis, Sigma-Aldrich®

Supplier: MilliporeSigma
Description: Cas Number 26266-58-0 100Ml

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Image Unavailable-TCS0064-500G

Span® 85

Supplier: TCI America
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

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Image Unavailable-76879-610

Sorbitan trioleate Saponification Value 165-180

Supplier: Ambeed
Description: Sorbitan trioleate Saponification Value 165-180

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Sorbitan trioleate

Supplier: Spectrum Chemicals
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.

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Image Unavailable-77436-808

Anti-LRP1 Rabbit Polyclonal Antibody

Catalog Number: (77436-808)
Supplier: Bioss
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.

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Image Unavailable-10310-548

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

Catalog Number: (10310-548)
Supplier: Bioss
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.
Image Unavailable-10316-392

Anti-C1orf85 Rabbit Polyclonal Antibody (Cy7®)

Catalog Number: (10316-392)
Supplier: Bioss
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.
Image Unavailable-10316-390

Anti-C1orf85 Rabbit Polyclonal Antibody (Cy5®)

Catalog Number: (10316-390)
Supplier: Bioss
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.
Image Unavailable-10310-546

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

Catalog Number: (10310-546)
Supplier: Bioss
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.
Image Unavailable-10316-388

Anti-C1orf85 Rabbit Polyclonal Antibody (Cy3®)

Catalog Number: (10316-388)
Supplier: Bioss
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.
Product Image-470236-286

Ward's® Sterile, Disposable Cell Spreaders

Supplier: VWR International
Description: Smooth-edged spreaders are excellent for spreading cultures and liquids without unwanted cutting, scraping, or gouging of agar during inoculation.

Image Unavailable-EM8.40122.0100

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

Catalog Number: (EM8.40122.0100)
Supplier: MilliporeSigma

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Span® 40

Catalog Number: (BT133545-250G)
Supplier: BeanTown Chemical
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)

SDS


Image Unavailable-TCS0061-500G

Span® 40

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

SDS Certificates


Image Unavailable-EM8.40123.0100

Span® 80 for synthesis, Sigma-Aldrich®

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

Certificates

Image Unavailable-TCS0060-025G

Span® 80

Supplier: TCI America
Description: CAS Number: 1338-43-8
MDL Number: MFCD00080948
Form: Clear Liquid
Color: Yellow
Flash Point (°C): 113
Specific Gravity (20/20): 0.99

SDS Certificates

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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.
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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