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Image Unavailable-BOSSBS-10446R-A750

Anti-HPV16-E7 Rabbit Polyclonal Antibody (Alexa Fluor® 750)

Catalog Number: (BOSSBS-10446R-A750)
Supplier: Bioss
Description: Plays a role in viral genome replication by driving entry of quiescent cells into the cell cycle. Stimulation of progression from G1 to S phase allows the virus to efficiently use the cellular DNA replicating machinery to achieve viral genome replication. E7 protein has both transforming and trans-activating activities. Induces the disassembly of the E2F1 transcription factor from RB1, with subsequent transcriptional activation of E2F1-regulated S-phase genes. Interferes with host histone deacetylation mediated by HDAC1 and HDAC2, leading to transcription activation. Plays also a role in the inhibition of both antiviral and antiproliferative functions of host interferon alpha.
UOM: 1 * 100 µl
Image Unavailable-BOSSBS-11284R-CY7

Anti-FGFBP2 Rabbit Polyclonal Antibody (Cy7®)

Catalog Number: (BOSSBS-11284R-CY7)
Supplier: Bioss
Description: KSP37 is a 223 amino acid protein that is secreted into the extracellular space and belongs to the fibroblast growth factor-binding protein family. Expressed in serum, as well as in cytotoxic T lymphocytes and peripheral leukocytes, KSP37 is thought to be involved in lymphocyte-mediated immunity, possibly playing a role in the development of asthma. The gene encoding KSP37 maps to human chromosome 4, which encodes nearly 6% of the human genome and has the largest gene deserts (regions of the genome with no protein encoding genes) of all of the human chromosomes. Defects in some of the genes located on chromosome 4 are associated with Huntington's disease, Ellis-van Creveld syndrome, methylmalonic acidemia and polycystic kidney disease.
UOM: 1 * 100 µl
Image Unavailable-BOSSBS-11284R-A680

Anti-FGFBP2/KSP37 Rabbit Polyclonal Antibody (Alexa Fluor® 680)

Catalog Number: (BOSSBS-11284R-A680)
Supplier: Bioss
Description: KSP37 is a 223 amino acid protein that is secreted into the extracellular space and belongs to the fibroblast growth factor-binding protein family. Expressed in serum, as well as in cytotoxic T lymphocytes and peripheral leukocytes, KSP37 is thought to be involved in lymphocyte-mediated immunity, possibly playing a role in the development of asthma. The gene encoding KSP37 maps to human chromosome 4, which encodes nearly 6% of the human genome and has the largest gene deserts (regions of the genome with no protein encoding genes) of all of the human chromosomes. Defects in some of the genes located on chromosome 4 are associated with Huntington's disease, Ellis-van Creveld syndrome, methylmalonic acidemia and polycystic kidney disease.
UOM: 1 * 100 µl
Image Unavailable-BOSSBS-15193R

Anti-C4orf40 Rabbit Polyclonal Antibody

Catalog Number: (BOSSBS-15193R)
Supplier: Bioss
Description: Representing approximately 6% of the human genome, chromosome 4 contains nearly 900 genes. Notably, the Huntingtin gene, which is found to encode an expanded glutamine tract in cases of Huntington's disease, is on chromosome 4. FGFR-3 is also encoded on chromosome 4 and has been associated with thanatophoric dwarfism, achondroplasia, Muenke syndrome and bladder cancer. Chromosome 4 is also tied to Ellis-van Creveld syndrome, methylmalonic acidemia and polycystic kidney disease. Chromosome 4 reportedly contains the largest gene deserts (regions of the genome with no protein encoding genes) and has one of the two lowest recombination frequencies of the human chromosomes. The C4orf40 gene product has been provisionally designated C4orf40 pending further characterization.
UOM: 1 * 100 µl
Image Unavailable-BOSSBS-8251R

Anti-DCUN1D4 Rabbit Polyclonal Antibody

Catalog Number: (BOSSBS-8251R)
Supplier: Bioss
Description: The DCN1-like protein family is comprised of Dcun1D1, Dcun1D2, Dcun1D3, Dcun1D4 and Dcun1D5. The founding member, Dcun1D1, is involved in the malignant transformation of squamous cell lineage.Dcun1D4, (defective in cullin neddylation protein 1-like protein 4 or DCN1-like protein 4), also designated KIAA0276, exists as 2 isoforms as a result of alternative splicing and contains one DCUN1 domain. The gene encoding Dcun1D4 maps to chromosome 4, which houses nearly 6% of the human genome and has the largest gene deserts (regions of the genome with no protein encoding genes) of all of the human chromosomes. Defects in some of the genes located on chromosome 4 are associated with Huntington's disease, Ellis-van Creveld syndrome, methylmalonic acidemia and polycystic kidney disease.
UOM: 1 * 100 µl
Image Unavailable-BOSSBS-15194R-CY5

Anti-C4orf46 Rabbit Polyclonal Antibody (Cy5®)

Catalog Number: (BOSSBS-15194R-CY5)
Supplier: Bioss
Description: Representing approximately 6% of the human genome, chromosome 4 contains nearly 900 genes. Notably, the Huntingtin gene, which is found to encode an expanded glutamine tract in cases of Huntington's disease, is on chromosome 4. FGFR-3 is also encoded on chromosome 4 and has been associated with thanatophoric dwarfism, achondroplasia, Muenke syndrome and bladder cancer. Chromosome 4 is also tied to Ellis-van Creveld syndrome, methylmalonic acidemia and polycystic kidney disease. Chromosome 4 reportedly contains the largest gene deserts (regions of the genome with no protein encoding genes) and has one of the two lowest recombination frequencies of the human chromosomes. The C4orf46 gene product has been provisionally designated C4orf46 pending further characterization.
UOM: 1 * 100 µl
Image Unavailable-BOSSBS-8251R-CY5

Anti-DCUN1D4 Rabbit Polyclonal Antibody (Cy5®)

Catalog Number: (BOSSBS-8251R-CY5)
Supplier: Bioss
Description: The DCN1-like protein family is comprised of Dcun1D1, Dcun1D2, Dcun1D3, Dcun1D4 and Dcun1D5. The founding member, Dcun1D1, is involved in the malignant transformation of squamous cell lineage.Dcun1D4, (defective in cullin neddylation protein 1-like protein 4 or DCN1-like protein 4), also designated KIAA0276, exists as 2 isoforms as a result of alternative splicing and contains one DCUN1 domain. The gene encoding Dcun1D4 maps to chromosome 4, which houses nearly 6% of the human genome and has the largest gene deserts (regions of the genome with no protein encoding genes) of all of the human chromosomes. Defects in some of the genes located on chromosome 4 are associated with Huntington's disease, Ellis-van Creveld syndrome, methylmalonic acidemia and polycystic kidney disease.
UOM: 1 * 100 µl
Image Unavailable-BOSSBS-0338R-CY5.5

Anti-HGV Polyprotein Rabbit Polyclonal Antibody (Cy5.5®)

Catalog Number: (BOSSBS-0338R-CY5.5)
Supplier: Bioss
Description: Hepatitis G virus is from a group of viruses called GB viruses (GB virus A, GB virus B and GB virus C) and is also designated as GB virus C (GBV C). HGV is a positive stranded RNA virus, with a genome of 10 KB and appears, on the basis of genome length and organisation, to be a member of the Flaviviridae and distinct from the hepatitis C virus (HCV). HGV infection appears to be transmitted following receipt of blood from HGV RNA positive donors, however, these patients have only moderate liver enzyme elevations and do not develop chronic liver disease.
UOM: 1 * 100 µl
Image Unavailable-BOSSBS-15194R-CY3

Anti-C4orf46 Rabbit Polyclonal Antibody (Cy3®)

Catalog Number: (BOSSBS-15194R-CY3)
Supplier: Bioss
Description: Representing approximately 6% of the human genome, chromosome 4 contains nearly 900 genes. Notably, the Huntingtin gene, which is found to encode an expanded glutamine tract in cases of Huntington's disease, is on chromosome 4. FGFR-3 is also encoded on chromosome 4 and has been associated with thanatophoric dwarfism, achondroplasia, Muenke syndrome and bladder cancer. Chromosome 4 is also tied to Ellis-van Creveld syndrome, methylmalonic acidemia and polycystic kidney disease. Chromosome 4 reportedly contains the largest gene deserts (regions of the genome with no protein encoding genes) and has one of the two lowest recombination frequencies of the human chromosomes. The C4orf46 gene product has been provisionally designated C4orf46 pending further characterization.
UOM: 1 * 100 µl
Image Unavailable-BOSSBS-8251R-CY7

Anti-DCUN1D4 Rabbit Polyclonal Antibody (Cy7®)

Catalog Number: (BOSSBS-8251R-CY7)
Supplier: Bioss
Description: The DCN1-like protein family is comprised of Dcun1D1, Dcun1D2, Dcun1D3, Dcun1D4 and Dcun1D5. The founding member, Dcun1D1, is involved in the malignant transformation of squamous cell lineage.Dcun1D4, (defective in cullin neddylation protein 1-like protein 4 or DCN1-like protein 4), also designated KIAA0276, exists as 2 isoforms as a result of alternative splicing and contains one DCUN1 domain. The gene encoding Dcun1D4 maps to chromosome 4, which houses nearly 6% of the human genome and has the largest gene deserts (regions of the genome with no protein encoding genes) of all of the human chromosomes. Defects in some of the genes located on chromosome 4 are associated with Huntington's disease, Ellis-van Creveld syndrome, methylmalonic acidemia and polycystic kidney disease.
UOM: 1 * 100 µl
Image Unavailable-BOSSBS-9414R-FITC

Anti-TSPAN5 Rabbit Polyclonal Antibody (FITC (Fluorescein Isothiocyanate))

Catalog Number: (BOSSBS-9414R-FITC)
Supplier: Bioss
Description: NET-4, also known as TSPAN5 or TM4SF9, is a 268 amino acid multi-pass membrane protein that belongs to the tetraspanin family and is thought to play a role in signal transduction events related to cell development, activation, growth and motility. The gene encoding NET-4 maps to human chromosome 4, which encodes nearly 6% of the human genome and has the largest gene deserts (regions of the genome with no protein encoding genes) of all of the human chromosomes. Defects in some of the genes located on chromosome 4 are associated with Huntington's disease, Ellis-van Creveld syndrome, methylmalonic acidemia and polycystic kidney disease.
UOM: 1 * 100 µl
Image Unavailable-BOSSBS-9414R-CY7

Anti-TSPAN5 Rabbit Polyclonal Antibody (Cy7®)

Catalog Number: (BOSSBS-9414R-CY7)
Supplier: Bioss
Description: NET-4, also known as TSPAN5 or TM4SF9, is a 268 amino acid multi-pass membrane protein that belongs to the tetraspanin family and is thought to play a role in signal transduction events related to cell development, activation, growth and motility. The gene encoding NET-4 maps to human chromosome 4, which encodes nearly 6% of the human genome and has the largest gene deserts (regions of the genome with no protein encoding genes) of all of the human chromosomes. Defects in some of the genes located on chromosome 4 are associated with Huntington's disease, Ellis-van Creveld syndrome, methylmalonic acidemia and polycystic kidney disease.
UOM: 1 * 100 µl
Image Unavailable-BOSSBS-0338R-HRP

Anti-HGV Polyprotein Rabbit Polyclonal Antibody (HRP (Horseradish Peroxidase))

Catalog Number: (BOSSBS-0338R-HRP)
Supplier: Bioss
Description: Hepatitis G virus is from a group of viruses called GB viruses (GB virus A, GB virus B and GB virus C) and is also designated as GB virus C (GBV C). HGV is a positive stranded RNA virus, with a genome of 10 KB and appears, on the basis of genome length and organisation, to be a member of the Flaviviridae and distinct from the hepatitis C virus (HCV). HGV infection appears to be transmitted following receipt of blood from HGV RNA positive donors, however, these patients have only moderate liver enzyme elevations and do not develop chronic liver disease.
UOM: 1 * 100 µl
Image Unavailable-BOSSBS-0338R-FITC

Anti-HGV Polyprotein Rabbit Polyclonal Antibody (FITC (Fluorescein Isothiocyanate))

Catalog Number: (BOSSBS-0338R-FITC)
Supplier: Bioss
Description: Hepatitis G virus is from a group of viruses called GB viruses (GB virus A, GB virus B and GB virus C) and is also designated as GB virus C (GBV C). HGV is a positive stranded RNA virus, with a genome of 10 KB and appears, on the basis of genome length and organisation, to be a member of the Flaviviridae and distinct from the hepatitis C virus (HCV). HGV infection appears to be transmitted following receipt of blood from HGV RNA positive donors, however, these patients have only moderate liver enzyme elevations and do not develop chronic liver disease.
UOM: 1 * 100 µl
Image Unavailable-BOSSBS-0338R-A750

Anti-HGV PolyProtein Rabbit Polyclonal Antibody (Alexa Fluor® 750)

Catalog Number: (BOSSBS-0338R-A750)
Supplier: Bioss
Description: Hepatitis G virus is from a group of viruses called GB viruses (GB virus A, GB virus B and GB virus C) and is also designated as GB virus C (GBV C). HGV is a positive stranded RNA virus, with a genome of 10 KB and appears, on the basis of genome length and organisation, to be a member of the Flaviviridae and distinct from the hepatitis C virus (HCV). HGV infection appears to be transmitted following receipt of blood from HGV RNA positive donors, however, these patients have only moderate liver enzyme elevations and do not develop chronic liver disease.
UOM: 1 * 100 µl
Image Unavailable-BOSSBS-0338R-A647

Anti-HGV Polyprotein Rabbit Polyclonal Antibody (Alexa Fluor® 647)

Catalog Number: (BOSSBS-0338R-A647)
Supplier: Bioss
Description: Hepatitis G virus is from a group of viruses called GB viruses (GB virus A, GB virus B and GB virus C) and is also designated as GB virus C (GBV C). HGV is a positive stranded RNA virus, with a genome of 10 KB and appears, on the basis of genome length and organisation, to be a member of the Flaviviridae and distinct from the hepatitis C virus (HCV). HGV infection appears to be transmitted following receipt of blood from HGV RNA positive donors, however, these patients have only moderate liver enzyme elevations and do not develop chronic liver disease.
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 at +43 1 97002 - 0.
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