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You Searched For: Poloxamer+181+(Pluronic®+L-61,+Synperonic®+L61)


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Image Unavailable-10304-894

Anti-SHROOM1 Rabbit Polyclonal Antibody (HRP (Horseradish Peroxidase))

Catalog Number: (10304-894)
Supplier: Bioss
Description: SHROOM1 is an 852 amino acid protein that contains one ASD1 domain and one ASD2 domain. Localized to both the cytoplasm and the cytoskeleton, SHROOM1 interacts with Actin and is thought to be involved in microtubule assembly during cell elongation, possibly playing a role in the development of the nervous system. Multiple isoforms of SHROOM1 exist due to alternative splicing events. The gene encoding SHROOM1 maps to human chromosome 5, which contains 181 million base pairs and comprises nearly 6% of the human genome. Deletion of the p arm of chromosome 5 leads to Cri du chat syndrome, while deletion of the q arm or of chromosome 5 altogether is common in therapy-related acute myelogenous leukemias and myelodysplastic syndrome.
Image Unavailable-89515-480

Anti-ST6GALNAC4 Rabbit Polyclonal Antibody

Catalog Number: (89515-480)
Supplier: Abgent
Description: Western Blot: 1:1000
Image Unavailable-BT221005-100G

Pentafluorobenzyl bromide ≥98%

Supplier: BeanTown Chemical
Description: CAS: 1765-40-8; EC No: 217-182-4; MDL No: MFCD00000299 UN No: UN3265; Haz Class: 8; Packing Group: II Liquid; Molecular Formula: C7H2BrF5 ; MW: 260.99 Melting Point: 19-20°; Boiling Point: 174-175°; Flash point: 83°C (181°F) Density (g/mL): 1.728; Refractive Index: 1.471

SDS

Image Unavailable-10072-090

Human Recombinant ACRP30 (from E. coli)

Catalog Number: (10072-090)
Supplier: Prosci
Description: The gAcrp30 variant is a naturally occurring globular protein, obtained by proteolytic processing of adiponectin. Adiponectin is produced and secreted exclusively by adipocytes, and is a relatively abundant plasma protein, accounting for up to 0.05% of total serum protein. Like Adiponectin, Acrp30 is capable of decreasing hyperglycemia and reversing insulin resistance. Additionally, gAcrp30 has been shown to be an important factor in promoting fat loss by signaling muscle to absorb and burn Free-Fatty Acids (FFAs). The signaling receptors for adiponectin and gAcrp30 have recently been identified and names AdipoR1 and AdipoR2. AdipoR2 is predominantly expressed in the liver. This naturally occurring variant of human gAcrp30/Adipolean is an 18.1 kDa protein, containing 14 amino acids extra at the N-terminus of human gAcrp30/Adipolean.
Image Unavailable-10272-108

Anti-HMP19 Rabbit Polyclonal Antibody (Cy3®)

Catalog Number: (10272-108)
Supplier: Bioss
Description: With 181 million base pairs encoding around 1,000 genes, chromosome 5 is about 6% of human genomic DNA. It is associated with Cockayne syndrome through the ERCC8 gene and familial adenomatous polyposis through the adenomatous polyposis coli (APC) tumor suppressor gene. Treacher Collins syndrome is also chromosome 5 associated and is caused by insertions or deletions within the TCOF1 gene. Deletion of the p arm of chromosome 5 leads to Cri du chat syndrome. Deletion of 5q or chromosome 5 altogether is common in therapy-related acute myelogenous leukemias and myelodysplastic syndrome.
Product Image-10206-276

Anti-PRDX2 Rabbit Polyclonal Antibody

Catalog Number: (10206-276)
Supplier: Boster Biological Technology
Description: Rabbit IgG polyclonal antibody for Peroxiredoxin-2(PRDX2) detection. Tested with WB in Human;Mouse;Rat.
Image Unavailable-76107-778

Anti-C5ORF4 Rabbit Polyclonal Antibody (Alexa Fluor® 750)

Catalog Number: (76107-778)
Supplier: Bioss
Description: With 181 million base pairs encoding around 1,000 genes, chromosome 5 is about 6% of human genomic DNA. It is associated with Cockayne syndrome through the ERCC8 gene and familial adenomatous polyposis through the adenomatous polyposis coli (APC) tumor suppressor gene. Treacher Collins syndrome is also chromosome 5 associated and is caused by insertions or deletions within the TCOF1 gene. Deletion of the p arm of chromosome 5 leads to Cri du chat syndrome. Deletion of 5q or chromosome 5 altogether is common in therapy-related acute myelogenous leukemias and myelodysplastic syndrome. The C5orf4 gene product has been provisionally designated C5orf4 pending further characterization.
Image Unavailable-10072-008

Mouse Recombinant MCSF (from E. coli)

Supplier: Prosci
Description: M-CSF is a potent hematopoietic factor produced by a variety of cells including lymphocytes, monocytes, fibroblasts, endothelial cells, myoblasts and osteoblasts. It is a key regulator of cellular proliferation, differentiation, and survival of blood monocytes, tissue macrophages and their progenitor cells. M-CSF has been shown to play important roles in modulating dermal thickness, and male and female fertility. M-CSF is clinically used in the treatment of infection, malignancies and atherosclerosis. It facilitates hematopoietic recovery after bone marrow transplantation. The human is reactive in murine systems, but the murine molecule exhibits no activity on human cells. Recombinant rat M-CSF is a 18.1 kDa homodimeric protein containing two 155 amino acid polypeptide subunits.

Image Unavailable-75790-140

Human Recombinant CD160 (from Cells)

Catalog Number: (75790-140)
Supplier: Prosci
Description: CD160 antigen is a Lipid-anchor that exists as a disulfide-linked homomultimer. CD160 contains one Ig-like V-type domain. The human CD160 precursor is a cysteine-rich, glycosylphosphatidylinositol-anchored protein of 181 amino acids with a single Ig-like domain. It is weakly homologous to KIR2DL4. CD160 is expressed in the spleen, peripheral blood, and small intestine. Its expression is tightly associated with peripheral blood NK cells and CD8 T lymphocytes with cytolytic effector activity. CD160 is a receptor showing broad specificity for both classical and non-classical MHC class I molecules.
Product Image-56617-331

Lab Pack, UN and DOT, Eagle Manufacturing

Catalog Number: (56617-331)
Supplier: Eagle Manufacturing
Description: Suitable for use with hazardous materials, Packing Groups I, II, and III.
Product Image-56617-339

Overpack and Salvage Drums, UN and DOT, Eagle Mfg

Supplier: Eagle Manufacturing
Description: Designed for use with hazardous materials, Packing Groups I, II, and III.

Image Unavailable-BT124355-25G

(1S,2R)-(-)-10,2-Camphorsultam ≥99%

Supplier: BeanTown Chemical
Description: CAS: 94594-90-8; MDL No: MFCD00066271 Crystalline; Molecular Formula: C10H17NO2S ; MW: 215.31 Melting Point: 181-183° Optical Rotation: [α]19/D −32°, c = 5 in chloroform

SDS

Image Unavailable-76099-126

Anti-C5orf48 Rabbit Polyclonal Antibody (Alexa Fluor® 680)

Catalog Number: (76099-126)
Supplier: Bioss
Description: C5orf48 (chromosome 5 open reading frame 48), also known as FLJ27505, MGC163367 or MGC163369, is a 134 amino acid protein. Encoded by a gene that maps to human chromosome 5q23.2, C5orf48 is linked to Autosomal dominant leukodystrophy (ADLD). Chromosome 5 makes up approximately 6% of the human genome and contains 181 million base pairs, which encode 1,000 genes. Chromosome 5 is associated with Cockayne syndrome through the ERCC8 gene and familial adenomatous polyposis through the adenomatous polyposis coli (APC) tumor suppressor gene. Treacher Collins syndrome is caused by insertions or deletions within the TCOF1 gene and is also associated with chromosome 5. Deletion of 5q or chromosome 5 altogether is common in therapy-related acute myelogenous leukemias and myelodysplastic syndrome.
Image Unavailable-76099-124

Anti-C5orf45 Rabbit Polyclonal Antibody (Alexa Fluor® 750)

Catalog Number: (76099-124)
Supplier: Bioss
Description: C5orf45 is a With 181 million base pairs encoding around 1,000 genes, chromosome 5 is about 6% of human genomic DNA. It is associated with Cockayne syndrome through the ERCC8 gene and familial adenomatous polyposis through the adenomatous polyposis coli (APC) tumor suppressor gene. Treacher Collins syndrome is also chromosome 5 associated and is caused by insertions or deletions within the TCOF1 gene. Deletion of the p arm of chromosome 5 leads to Cri du chat syndrome. Deletion of 5q or chromosome 5 altogether is common in therapy-related acute myelogenous leukemias and myelodysplastic syndrome. The C5orf45 gene product has been provisionally designated C5orf45 pending further characterization.
Image Unavailable-76099-106

Anti-C5orf34 Rabbit Polyclonal Antibody (Alexa Fluor® 680)

Catalog Number: (76099-106)
Supplier: Bioss
Description: C5orf34 is a With 181 million base pairs encoding around 1,000 genes, chromosome 5 is about 6% of human genomic DNA. It is associated with Cockayne syndrome through the ERCC8 gene and familial adenomatous polyposis through the adenomatous polyposis coli (APC) tumor suppressor gene. Treacher Collins syndrome is also chromosome 5 associated and is caused by insertions or deletions within the TCOF1 gene. Deletion of the p arm of chromosome 5 leads to Cri du chat syndrome. Deletion of 5q or chromosome 5 altogether is common in therapy-related acute myelogenous leukemias and myelodysplastic syndrome. The C5orf34 gene product has been provisionally designated C5orf34 pending further characterization.
Image Unavailable-76107-782

Anti-C5orf35 Rabbit Polyclonal Antibody (Alexa Fluor® 750)

Catalog Number: (76107-782)
Supplier: Bioss
Description: With 181 million base pairs encoding around 1,000 genes, chromosome 5 is about 6% of human genomic DNA. It is associated with Cockayne syndrome through the ERCC8 gene and familial adenomatous polyposis through the adenomatous polyposis coli (APC) tumor suppressor gene. Treacher Collins syndrome is also chromosome 5 associated and is caused by insertions or deletions within the TCOF1 gene. Deletion of the p arm of chromosome 5 leads to Cri du chat syndrome. Deletion of 5q or chromosome 5 altogether is common in therapy-related acute myelogenous leukemias and myelodysplastic syndrome. The C5orf35 gene product has been provisionally designated C5orf35 pending further characterization.
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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.
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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