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Image Unavailable-USBIC7907-09-250

Anti-C-Reactive Protein Mouse monoclonal antibody [clone: 1.BB.97]

Catalog Number: (USBIC7907-09-250)
Supplier: US Biological
Description: Anti-C-Reactive Protein Mouse monoclonal antibody [clone: 1.BB.97]
UOM: 1 * 250 µG
Image Unavailable-BOSSBS-11512R-A750

Anti-BBS10 Rabbit Polyclonal Antibody (Alexa Fluor® 750)

Catalog Number: (BOSSBS-11512R-A750)
Supplier: Bioss
Description: Bardet-Biedl syndrome (BBS) is a pleiotropic genetic disorder characterised by obesity, photoreceptor degeneration, polydactyly, hypogenitalism, renal abnormalities, and developmental delay. Other associated clinical findings in BBS patients include diabetes, hypertension, and congenital heart defects. BBS genes map to multiple loci and encode fourteen proteins, BBS1-BBS14. Many BBS genes encode basal body or cilia proteins, suggesting that BBS is a ciliary dysfunction disorder. BBS10 (Bardet-Biedl syndrome 10), also known as chromosome 12 open reading fame 58, C12orf58 or FLJ23560, is a novel 723 amino acid protein belonging to the TCP-1 chaperonin family. BBS10 localizes to the basal body of primary cilium and assists in protein folding upon ATP hydrolysis. Inhibition of BBS10 has been found to impair ciliogenesis, activate the glycogen synthase kinase 3 pathway and cause peroxisome proliferator-activated receptor nuclear accumulation. The gene encoding BBS10 contains two exons and maps to human chromosome 12q21.2.
UOM: 1 * 100 µl
Image Unavailable-USBIC7910-14F

Anti-Creatine Kinase BB Isoenzyme Mouse monoclonal antibody [clone: 10B2594]

Catalog Number: (USBIC7910-14F)
Supplier: US Biological
Description: Anti-Creatine Kinase BB Isoenzyme Mouse monoclonal antibody [clone: 10B2594]
UOM: 1 * 200 µG
Image Unavailable-BOSSBS-11506R

Anti-BBS2 Rabbit Polyclonal Antibody

Catalog Number: (BOSSBS-11506R)
Supplier: Bioss
Description: Bardet-Biedl syndrome (BBS) is a pleiotropic genetic disorder characterized by obesity, photoreceptor degeneration, polydactyly, hypogenitalism, renal abnormalities, and developmental delay. Other associated clinical findings in BBS patients include diabetes, hypertension, and congenital heart defects. BBS is a heterogeneous disorder that maps to eight genetic loci and encodes eight proteins, BBS1-BBS8. Five BBS genes encode basal body or cilia proteins, suggesting that BBS is a ciliary dysfunction disorder. BBS2 is a 721-amino acid protein that is evolutionarily conserved and is expressed in a broad range of tissues including: brain, kidney, adrenal gland, and thyroid gland. Loss of BBS2 may be involved in defects in social interactions as well as infertility. BBS2 retinopathy involves normal retina development followed by apoptotic death of photoreceptors, the primary ciliated cells of the retina.
UOM: 1 * 100 µl
Image Unavailable-BOSSBS-11506R-HRP

Anti-BBS2 Rabbit Polyclonal Antibody (HRP (Horseradish Peroxidase))

Catalog Number: (BOSSBS-11506R-HRP)
Supplier: Bioss
Description: Bardet-Biedl syndrome (BBS) is a pleiotropic genetic disorder characterized by obesity, photoreceptor degeneration, polydactyly, hypogenitalism, renal abnormalities, and developmental delay. Other associated clinical findings in BBS patients include diabetes, hypertension, and congenital heart defects. BBS is a heterogeneous disorder that maps to eight genetic loci and encodes eight proteins, BBS1-BBS8. Five BBS genes encode basal body or cilia proteins, suggesting that BBS is a ciliary dysfunction disorder. BBS2 is a 721-amino acid protein that is evolutionarily conserved and is expressed in a broad range of tissues including: brain, kidney, adrenal gland, and thyroid gland. Loss of BBS2 may be involved in defects in social interactions as well as infertility. BBS2 retinopathy involves normal retina development followed by apoptotic death of photoreceptors, the primary ciliated cells of the retina.
UOM: 1 * 100 µl
Image Unavailable-USBIC7850-60C

Anti-Complement Factor B, Bb Fragment Mouse Monoclonal Antibody [clone: 10B2566]

Catalog Number: (USBIC7850-60C)
Supplier: US Biological
Description: Anti-Complement Factor B, Bb Fragment Mouse Monoclonal Antibody [clone: 10B2566]
UOM: 1 * 100 µG
Image Unavailable-SPCMFD115-100GM

Indigo carmine

Supplier: Spectrum Chemical
Description: FD and C Blue No. 2 - In the United States, the Food and Drug Administration (FDA) controls the specifications for Food, Drug and Cosmetic (FD&C) colours.

Image Unavailable-SHBTPB-500-19

Human Glioma Culture Media Recombinant Protein Bundle (rh EGF, rh FGF-basic 154, rh PDGF-AA, rh PDGF-BB) (from E. coli)

Catalog Number: (SHBTPB-500-19)
Supplier: Shenandoah Biotechnology
Description: Cytokines for cell culture of human DIPG and other glioma cells. A glioma is a generic term used to describe tumors that arise from the glia tissue of the brain that supports and surrounds neurons. Diffuse Intrinsic Pontine Glioma (DIPG) is a pediatric brain tumor that originates in the brainstem. Cells isolated from these childhood tumors are successfully cultured ex vivo with EGF, FGF-basic (or FGF-2), and PDGFs (AA and BB).
UOM: 1 * 1 KIT

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Image Unavailable-A16052.14

Indigo carmine

Supplier: Thermo Fisher Scientific
Description: Indigo carmine

MSDS Certificates

Product Image-786-496

Coomassie brilliant blue G-250 electrophoresis gel stain

Catalog Number: (786-496)
Supplier: G-Biosciences
Description: G-Biosciences' Coomassie Brilliant Blue (CBB) G-250 and R-250 Stain are based on a colloidal Coomassie stain. CBB G-250 and R-250 stain proteins with high band visibility. The staining of gels with CBB G-250 and R-250 allows the examination of protein bands even during the staining process.
UOM: 1 * 10 g
Image Unavailable-BOSSBS-11508R-CY3

Anti-BBS4 Rabbit Polyclonal Antibody (Cy3®)

Catalog Number: (BOSSBS-11508R-CY3)
Supplier: Bioss
Description: Bardet-Biedl syndrome (BBS) is a pleiotropic genetic disorder characterized by obesity, photoreceptor degeneration, polydactyly, hypogenitalism, renal abnormalities, and developmental delay. Other associated clinical findings in BBS patients include diabetes, hypertension, and congenital heart defects. BBS is a heterogeneous disorder; BBS genes map to eight genetic loci and encode eight proteins, BBS1-BBS8. Five BBS genes encode basal body or cilia proteins, suggesting that BBS is a ciliary dysfunction disorder. BBS4 is expressed in the olfactory epithelium and localizes to the centriolar satellites of centrosomes and basal bodies of primary cilia. BBS4 regulates the p150 subunit of the dynein transport machinery (DCTN1) to attract pericentriolar material-1 protein (PCM1) and its associated components to the satellites. Loss of BBS4 is correlated with obesity caused by abnormal lipid profiles, liver dysfunction, elevated insulin, and abnormal leptin levels.
UOM: 1 * 100 µl
Product Image-PIER34035

Substrate for western blotting, NBT (nitro-blue tetrazolium chloride)

Catalog Number: (PIER34035)
Supplier: Thermo Fisher Scientific
Description: NBT (nitro-blue tetrazolium chloride) yields a blue-purple, water-insoluble product upon reduction of the tetrazolium salt. The product of reduction is NBT-formazan. This substrate is widely used for immunochemistry applications because the color is linear and stable. NBT is used as the substrate for both glucose oxidase and alkaline phosphatase systems.
UOM: 1 * 1 g
Image Unavailable-ICNA0215051825

Bromocresol purple sodium salt, orange powder

Supplier: MP Biomedicals
Description: Bromocresol purple sodium salt is typically used as a pH indicator (5,2 - 6,8 : yellow to blue-purple). Used in spectrophotometric determination of serum-albumin.

Image Unavailable-BOSSBS-11512R-A555

Anti-BBS10 Rabbit Polyclonal Antibody (Alexa Fluor® 555)

Catalog Number: (BOSSBS-11512R-A555)
Supplier: Bioss
Description: Bardet-Biedl syndrome (BBS) is a pleiotropic genetic disorder characterized by obesity, photoreceptor degeneration, polydactyly, hypogenitalism, renal abnormalities, and developmental delay. Other associated clinical findings in BBS patients include diabetes, hypertension, and congenital heart defects. BBS genes map to multiple loci and encode fourteen proteins, BBS1-BBS14. Many BBS genes encode basal body or cilia proteins, suggesting that BBS is a ciliary dysfunction disorder. BBS10 (Bardet-Biedl syndrome 10), also known as chromosome 12 open reading fame 58, C12orf58 or FLJ23560, is a novel 723 amino acid protein belonging to the TCP-1 chaperonin family. BBS10 localizes to the basal body of primary cilium and assists in protein folding upon ATP hydrolysis. Inhibition of BBS10 has been found to impair ciliogenesis, activate the glycogen synthase kinase 3 pathway and cause peroxisome proliferator-activated receptor nuclear accumulation. The gene encoding BBS10 contains two exons and maps to human chromosome 12q21.2.
UOM: 1 * 100 µl
Image Unavailable-BOSSBS-11508R-A647

Anti-BBS4 Rabbit Polyclonal Antibody (Alexa Fluor® 647)

Catalog Number: (BOSSBS-11508R-A647)
Supplier: Bioss
Description: Bardet-Biedl syndrome (BBS) is a pleiotropic genetic disorder characterized by obesity, photoreceptor degeneration, polydactyly, hypogenitalism, renal abnormalities, and developmental delay. Other associated clinical findings in BBS patients include diabetes, hypertension, and congenital heart defects. BBS is a heterogeneous disorder; BBS genes map to eight genetic loci and encode eight proteins, BBS1-BBS8. Five BBS genes encode basal body or cilia proteins, suggesting that BBS is a ciliary dysfunction disorder. BBS4 is expressed in the olfactory epithelium and localizes to the centriolar satellites of centrosomes and basal bodies of primary cilia. BBS4 regulates the p150 subunit of the dynein transport machinery (DCTN1) to attract pericentriolar material-1 protein (PCM1) and its associated components to the satellites. Loss of BBS4 is correlated with obesity caused by abnormal lipid profiles, liver dysfunction, elevated insulin, and abnormal leptin levels.
UOM: 1 * 100 µl
Image Unavailable-BOSSBS-11510R-CY7

Anti-BBS8 Rabbit Polyclonal Antibody (Cy7®)

Catalog Number: (BOSSBS-11510R-CY7)
Supplier: Bioss
Description: Bardet-Biedl syndrome (BBS) is a pleiotropic genetic disorder characterized by obesity, photoreceptor degeneration, polydactyly, hypogenitalism, renal abnormalities, and developmental delay. BBS patients also have an increased risk of developing diabetes, hypertension, and congenital heart defects. BBS is a heterogeneous disorder mapping to eight genetic loci and encoding eight proteins, BBS1-BBS8. Five BBS proteins encode basal body or cilia proteins, suggesting that BBS is a ciliary dysfunction disorder. BBS2 contains two overlapping genes: BBS2L1 and BBS2L2. BBSL1 was re-named BBS7, whereas BBS2L2 independently funcitons as BBS1. BBS7 contains 672 amino acids and is expressed at low to moderate levels in most human tissues.
UOM: 1 * 100 µl
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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 on +353 1 88 22222.
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 eurega_services@eu.vwr.com
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The original product is no longer available. The replacement shown is available.
Product(s) marked with this symbol are discontinued - sold till end of stock. Alternatives may be available by searching with the VWR Catalog Number listed above. If you need further assistance, please call VWR Customer Service on +353 1 8822222.
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