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Image Unavailable-BOSSBS-12278R-A488

Anti-SOHLH1 Rabbit Polyclonal Antibody (Alexa Fluor® 488)

Omschrijving: SOHLH1 is a 328 amino acid protein that localizes to both the nucleus and the cytoplasm and contains one bHLH domain through which it may function as a transcription factor during oogenesis and spermatogenesis. The gene encoding SOHLH1 maps to human chromosome 9, which houses over 900 genes and comprises nearly 4% of the human genome. Hereditary hemorrhagic telangiectasia, which is characterized by harmful vascular defects, and Familial dysautonomia, are both associated with chromosome 9. Notably, chromosome 9 encompasses the largest interferon family gene cluster.
Catalogus nummer: BOSSBS-12278R-A488
UOM: 1 * 100 µl
Leverancier: Bioss
Image Unavailable-BOSSBS-9669R-A488

Anti-DENND4C Rabbit Polyclonal Antibody (Alexa Fluor® 488)

Omschrijving: DENND4C is a 1,673 amino acid multi-pass membrane protein. DENND4C contains a dDENN domain, DENN domain, uDENN domain and a PPR (pentatricopeptide) repeat. As a result of alternative splicing, six DENND4C isoforms exist. The gene encoding DENND4C maps to human chromosome 9, which houses over 900 genes and comprises nearly 4% of the human genome. Hereditary hemorrhagic telangiectasia, which is characterized by harmful vascular defects, and Familial dysautonomia, are both associated with chromosome 9. Notably, chromosome 9 encompasses the largest interferon family gene cluster.
Catalogus nummer: BOSSBS-9669R-A488
UOM: 1 * 100 µl
Leverancier: Bioss
Image Unavailable-BOSSBS-9669R-A750

Anti-DENND4C Rabbit Polyclonal Antibody (Alexa Fluor® 750)

Omschrijving: DENND4C is a 1673 amino acid multi-pass membrane protein. DENND4C contains a dDENN domain, DENN domain, uDENN domain and a PPR (pentatricopeptide) repeat. As a result of alternative splicing, six DENND4C isoforms exist. The gene encoding DENND4C maps to human chromosome 9, which houses over 900 genes and comprises nearly 4% of the human genome. Hereditary hemorrhagic telangiectasia, which is characterised by harmful vascular defects, and Familial dysautonomia, are both associated with chromosome 9. Notably, chromosome 9 encompasses the largest interferon family gene cluster.
Catalogus nummer: BOSSBS-9669R-A750
UOM: 1 * 100 µl
Leverancier: Bioss
Image Unavailable-BOSSBS-9995R-A750

Anti-C4orf32 Rabbit Polyclonal Antibody (Alexa Fluor® 750)

Omschrijving: C4orf32 is a 132 amino acid single pass membrane protein that is encoded by a gene that maps to human chromosome 4. Human chromosome 4 represents approximately 6% of the human genome and contains nearly 900 genes. Notably, the Huntingtin gene, which is found to encode an expanded glutamine tract in cases of Huntington's disease, is located on chromosome 4. FGFR-3 is also encoded by a gene that maps to human 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.
Catalogus nummer: BOSSBS-9995R-A750
UOM: 1 * 100 µl
Leverancier: Bioss
Image Unavailable-BOSSBS-9098R-CY3

Anti-ANKS3 Rabbit Polyclonal Antibody (Cy3®)

Omschrijving: ANKS3 is a 656 amino acid protein that contain six ANK repeats and one SAM (sterile alpha motif) domain. The gene encoding ANKS3 maps to human chromosome 16. Chromosome 16, which is associated with a variety of genetic disorders, encodes over 900 genes and comprises nearly 3% of the human genome. The GAN gene is located on chromosome 16 and, with mutation, may lead to giant axonal neuropathy, a nervous system disorder characterized by increasing malfunction with growth. The rare disorder Rubinstein-Taybi syndrome is associated with chromosome 16, as is Crohn's disease, which is a gastrointestinal inflammatory condition.
Catalogus nummer: BOSSBS-9098R-CY3
UOM: 1 * 100 µl
Leverancier: Bioss
Image Unavailable-BOSSBS-12278R-A750

Anti-Sohlh1 Rabbit Polyclonal Antibody (Alexa Fluor® 750)

Omschrijving: SOHLH1 is a 328 amino acid protein that localizes to both the nucleus and the cytoplasm and contains one bHLH domain through which it may function as a transcription factor during oogenesis and spermatogenesis. The gene encoding SOHLH1 maps to human chromosome 9, which houses over 900 genes and comprises nearly 4% of the human genome. Hereditary hemorrhagic telangiectasia, which is characterised by harmful vascular defects, and Familial dysautonomia, are both associated with chromosome 9. Notably, chromosome 9 encompasses the largest interferon family gene cluster.
Catalogus nummer: BOSSBS-12278R-A750
UOM: 1 * 100 µl
Leverancier: Bioss
Image Unavailable-BOSSBS-13323R-A750

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

Omschrijving: GCSH is a 173 amino acid mitochondrial protein that contains one lipoyl-binding domain and belongs to the gcvH family. Defects in the gene encoding GCSH are the cause of glycine encephalopathy (GCE), an autosomal recessive disease that is also referred to as non-ketotic hyperglycinemia (NKH). Characterized by severe neurological symptoms, patients with GCE have a large amount of glycine accumulated in their body fluids. The gene encoding GCSH maps to human chromosome 16, which encodes over 900 genes and comprises nearly 3% of the human genome.
Catalogus nummer: BOSSBS-13323R-A750
UOM: 1 * 100 µl
Leverancier: Bioss
Image Unavailable-BOSSBS-13323R-CY3

Anti-GCSH Rabbit Polyclonal Antibody (Cy3®)

Omschrijving: GCSH is a 173 amino acid mitochondrial protein that contains one lipoyl-binding domain and belongs to the gcvH family. Defects in the gene encoding GCSH are the cause of glycine encephalopathy (GCE), an autosomal recessive disease that is also referred to as non-ketotic hyperglycinemia (NKH). Characterized by severe neurological symptoms, patients with GCE have a large amount of glycine accumulated in their body fluids. The gene encoding GCSH maps to human chromosome 16, which encodes over 900 genes and comprises nearly 3% of the human genome.
Catalogus nummer: BOSSBS-13323R-CY3
UOM: 1 * 100 µl
Leverancier: Bioss
Image Unavailable-BOSSBS-13323R-A350

Anti-GCSH Rabbit Polyclonal Antibody (Alexa Fluor® 350)

Omschrijving: GCSH is a 173 amino acid mitochondrial protein that contains one lipoyl-binding domain and belongs to the gcvH family. Defects in the gene encoding GCSH are the cause of glycine encephalopathy (GCE), an autosomal recessive disease that is also referred to as non-ketotic hyperglycinemia (NKH). Characterized by severe neurological symptoms, patients with GCE have a large amount of glycine accumulated in their body fluids. The gene encoding GCSH maps to human chromosome 16, which encodes over 900 genes and comprises nearly 3% of the human genome.
Catalogus nummer: BOSSBS-13323R-A350
UOM: 1 * 100 µl
Leverancier: Bioss
Image Unavailable-BOSSBS-9993R-A680

Anti-C4orf19 Rabbit Polyclonal Antibody (Alexa Fluor® 680)

Omschrijving: C4orf19 is a 314 amino acid protein encoded by a gene that maps to human chromosome 4. Human chromosome 4 represents approximately 6% of the human genome and 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 by a gene that is located 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.
Catalogus nummer: BOSSBS-9993R-A680
UOM: 1 * 100 µl
Leverancier: Bioss
Image Unavailable-BOSSBS-9669R-A647

Anti-DENND4C Rabbit Polyclonal Antibody (Alexa Fluor® 647)

Omschrijving: DENND4C is a 1,673 amino acid multi-pass membrane protein. DENND4C contains a dDENN domain, DENN domain, uDENN domain and a PPR (pentatricopeptide) repeat. As a result of alternative splicing, six DENND4C isoforms exist. The gene encoding DENND4C maps to human chromosome 9, which houses over 900 genes and comprises nearly 4% of the human genome. Hereditary hemorrhagic telangiectasia, which is characterized by harmful vascular defects, and Familial dysautonomia, are both associated with chromosome 9. Notably, chromosome 9 encompasses the largest interferon family gene cluster.
Catalogus nummer: BOSSBS-9669R-A647
UOM: 1 * 100 µl
Leverancier: Bioss
Image Unavailable-BOSSBS-9669R-CY5.5

Anti-DENND4C Rabbit Polyclonal Antibody (Cy5.5®)

Omschrijving: DENND4C is a 1,673 amino acid multi-pass membrane protein. DENND4C contains a dDENN domain, DENN domain, uDENN domain and a PPR (pentatricopeptide) repeat. As a result of alternative splicing, six DENND4C isoforms exist. The gene encoding DENND4C maps to human chromosome 9, which houses over 900 genes and comprises nearly 4% of the human genome. Hereditary hemorrhagic telangiectasia, which is characterized by harmful vascular defects, and Familial dysautonomia, are both associated with chromosome 9. Notably, chromosome 9 encompasses the largest interferon family gene cluster.
Catalogus nummer: BOSSBS-9669R-CY5.5
UOM: 1 * 100 µl
Leverancier: Bioss
Image Unavailable-BOSSBS-9669R-HRP

Anti-DENND4C Rabbit Polyclonal Antibody (HRP (Horseradish Peroxidase))

Omschrijving: DENND4C is a 1,673 amino acid multi-pass membrane protein. DENND4C contains a dDENN domain, DENN domain, uDENN domain and a PPR (pentatricopeptide) repeat. As a result of alternative splicing, six DENND4C isoforms exist. The gene encoding DENND4C maps to human chromosome 9, which houses over 900 genes and comprises nearly 4% of the human genome. Hereditary hemorrhagic telangiectasia, which is characterized by harmful vascular defects, and Familial dysautonomia, are both associated with chromosome 9. Notably, chromosome 9 encompasses the largest interferon family gene cluster.
Catalogus nummer: BOSSBS-9669R-HRP
UOM: 1 * 100 µl
Leverancier: Bioss
Image Unavailable-BOSSBS-15187R-CY7

Anti-C4orf17 Rabbit Polyclonal Antibody (Cy7®)

Omschrijving: C4orf17 (chromosome 4 open reading frame 17) is a 359 amino acid protein encoded by a gene that maps to human chromosome 4. Human chromosome 4 represents approximately 6% of the human genome and 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 by a gene that is located 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.
Catalogus nummer: BOSSBS-15187R-CY7
UOM: 1 * 100 µl
Leverancier: Bioss
Image Unavailable-BOSSBS-15187R-A680

Anti-C4orf17 Rabbit Polyclonal Antibody (Alexa Fluor® 680)

Omschrijving: C4orf17 (chromosome 4 open reading frame 17) is a 359 amino acid protein encoded by a gene that maps to human chromosome 4. Human chromosome 4 represents approximately 6% of the human genome and 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 by a gene that is located 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.
Catalogus nummer: BOSSBS-15187R-A680
UOM: 1 * 100 µl
Leverancier: Bioss
Image Unavailable-BOSSBS-9098R-CY7

Anti-ANKS3 Rabbit Polyclonal Antibody (Cy7®)

Omschrijving: ANKS3 is a 656 amino acid protein that contain six ANK repeats and one SAM (sterile alpha motif) domain. The gene encoding ANKS3 maps to human chromosome 16. Chromosome 16, which is associated with a variety of genetic disorders, encodes over 900 genes and comprises nearly 3% of the human genome. The GAN gene is located on chromosome 16 and, with mutation, may lead to giant axonal neuropathy, a nervous system disorder characterized by increasing malfunction with growth. The rare disorder Rubinstein-Taybi syndrome is associated with chromosome 16, as is Crohn's disease, which is a gastrointestinal inflammatory condition.
Catalogus nummer: BOSSBS-9098R-CY7
UOM: 1 * 100 µl
Leverancier: Bioss
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