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


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Product Image-10744-702

Anti-WT1 Mouse Monoclonal Antibody [clone: 6F-H2]

Catalog Number: (10744-702)
Supplier: Abnova
Description: Mouse monoclonal antibody raised against partial recombinant WT1.
Image Unavailable-89520-616

Anti-DCLK1 Rabbit Polyclonal Antibody

Catalog Number: (89520-616)
Supplier: Abgent
Description: Western Blot: 1:1000
Image Unavailable-75789-574

Human Recombinant Osteoactivin (from Cells)

Catalog Number: (75789-574)
Supplier: Prosci
Description: Osteoactivin is an intracellular glycoprotein belongs to the NMB/pMEL-17 family, which is asscociated with cell endosomal/lysomal compartments. Human Osteoactivin is a 560 amino acid type I transmembrane protein, and one alternate splice form shows a 12 amino acid insert between amino acid 339-340. An additional 206 amino acid isoform shows a mutation at position 181 that results in a 26 amino acid substitution for the C-terminal 380 amino acids. Cells knowns to express Osteoactivin include fibroblast, osteoblasts, myeloid dendritic cell, melanocytes, plus fetal chondrocytes and stratum basale keratinocytes, macrophages/keratinocytes.
Image Unavailable-76099-110

Anti-C5orf35 Rabbit Polyclonal Antibody (Alexa Fluor® 680)

Catalog Number: (76099-110)
Supplier: Bioss
Description: C5orf35 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 C5orf35 gene product has been provisionally designated C5orf35 pending further characterization.
Image Unavailable-76099-108

Anti-C5orf34 Rabbit Polyclonal Antibody (Alexa Fluor® 750)

Catalog Number: (76099-108)
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-76099-130

Anti-C5orf49 Rabbit Polyclonal Antibody (Alexa Fluor® 680)

Catalog Number: (76099-130)
Supplier: Bioss
Description: C5orf49 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 C5orf49 gene product has been provisionally designated C5orf49 pending further characterization.
Image Unavailable-TCS0398-001G

N-Succinimidyl 3-Maleimidobenzoate ≥98.0% (by HPLC, total nitrogen)

Supplier: TCI America
Description: [Cross-linking Reagent]
CAS Number: 58626-38-3
MDL Number: MFCD00005514
Molecular Formula: C15H10N2O6
Molecular Weight: 314.25
Purity/Analysis Method: >98.0% (HPLC,N)
Form: Crystal
Color: White
Melting point (°C): 181
Storage Temperature: 0-10°C

SDS

Product Image-470219-434

Compound Bar

Catalog Number: (470219-434)
Supplier: Wards
Description: For demonstrating the differential expansion of two metals as shown by the curvature produced when the bar is heated. Each metal band is 200 x 15mm and riveted together.
Image Unavailable-10481-458

Anti-FAM50C Rabbit Polyclonal Antibody

Catalog Number: (10481-458)
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 FAM53C gene product has been provisionally designated FAM53C pending further characterization.
Image Unavailable-76107-780

Anti-C5orf35 Rabbit Polyclonal Antibody (Alexa Fluor® 680)

Catalog Number: (76107-780)
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.
Image Unavailable-89515-480

Anti-ST6GALNAC4 Rabbit Polyclonal Antibody

Catalog Number: (89515-480)
Supplier: Abgent
Description: Western Blot: 1:1000
Image Unavailable-10166-936

Anti-ATF3 Rabbit Polyclonal Antibody

Catalog Number: (10166-936)
Supplier: Genetex
Description: Rabbit Polyclonal antibody to ATF3 (activating transcription factor 3)
Image Unavailable-10294-744

Anti-GAPT Rabbit Polyclonal Antibody

Catalog Number: (10294-744)
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 C5orf29 gene product has been provisionally designated C5orf29 pending further characterization.
Image Unavailable-10317-512

Anti-C5orf24 Rabbit Polyclonal Antibody (Cy3®)

Catalog Number: (10317-512)
Supplier: Bioss
Description: C5orf24 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 C5orf24 gene product has been provisionally designated C5orf24 pending further characterization.
Image Unavailable-10317-516

Anti-C5orf24 Rabbit Polyclonal Antibody (Cy7®)

Catalog Number: (10317-516)
Supplier: Bioss
Description: C5orf24 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 C5orf24 gene product has been provisionally designated C5orf24 pending further characterization.
Image Unavailable-10317-588

Anti-C5orf49 Rabbit Polyclonal Antibody (FITC (Fluorescein Isothiocyanate))

Catalog Number: (10317-588)
Supplier: Bioss
Description: C5orf49 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 C5orf49 gene product has been provisionally designated C5orf49 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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