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Descripción: Anti-PAIP1 Rabbit Monoclonal Antibody [clone: EPR13258(B)]
Numero del catalogo: ABCAAB175211-100
UOM: 1 * 100 µl
Proveedor: Abcam


Descripción: Anti-PAIP1 Rabbit Polyclonal Antibody
Numero del catalogo: AVIVARP40650_P050
UOM: 1 * 50 µG
Proveedor: Aviva Systems Biology


Descripción: Anti-PAIP1 Rabbit Polyclonal Antibody
Numero del catalogo: AVIVARP40651_T100
UOM: 1 * 100 µG
Proveedor: Aviva Systems Biology


Descripción: Anti-PAIP1 Rabbit Monoclonal Antibody [clone: EPR13259]
Numero del catalogo: ABCAAB250487-100
UOM: 1 * 100 µG
Proveedor: Abcam


Descripción: FSIP1 is a 581 amino acid protein that is expressed in airway epithelium. A member of the FSIP1 family, FSIP1 is encoded by a gene that maps to human chromosome 15q14 and mouse chromosome 2 E5. Encoding more than 700 genes, chromosome 15 is made up of approximately 106 million base pairs and is about 3% of the human genome. Angelman and Prader-Willi syndromes are associated with loss of function or deletion of genes in the 15q11-q13 region. In the case of Angelman syndrome, this loss is due to inactivity of the maternal 15q11-q13 encoded UBE3A gene in the brain by either chromosomal deletion or mutation. In cases of Prader-Willi syndrome, there is a partial or complete deletion of this region from the paternal copy of chromosome 15. Tay-Sachs disease is a lethal disorder associated with mutations of the HEXA gene, which is encoded by chromosome 15. Marfan syndrome is associated with chromosome 15 through the FBN1 gene.
Numero del catalogo: BOSSBS-8575R-CY5
UOM: 1 * 100 µl
Proveedor: Bioss


Descripción: FSIP1 is a 581 amino acid protein that is expressed in airway epithelium. A member of the FSIP1 family, FSIP1 is encoded by a gene that maps to human chromosome 15q14 and mouse chromosome 2 E5. Encoding more than 700 genes, chromosome 15 is made up of approximately 106 million base pairs and is about 3% of the human genome. Angelman and Prader-Willi syndromes are associated with loss of function or deletion of genes in the 15q11-q13 region. In the case of Angelman syndrome, this loss is due to inactivity of the maternal 15q11-q13 encoded UBE3A gene in the brain by either chromosomal deletion or mutation. In cases of Prader-Willi syndrome, there is a partial or complete deletion of this region from the paternal copy of chromosome 15. Tay-Sachs disease is a lethal disorder associated with mutations of the HEXA gene, which is encoded by chromosome 15. Marfan syndrome is associated with chromosome 15 through the FBN1 gene.
Numero del catalogo: BOSSBS-8575R-CY5.5
UOM: 1 * 100 µl
Proveedor: Bioss


Descripción: FSIP1 is a 581 amino acid protein that is expressed in airway epithelium. A member of the FSIP1 family, FSIP1 is encoded by a gene that maps to human chromosome 15q14 and mouse chromosome 2 E5. Encoding more than 700 genes, chromosome 15 is made up of approximately 106 million base pairs and is about 3% of the human genome. Angelman and Prader-Willi syndromes are associated with loss of function or deletion of genes in the 15q11-q13 region. In the case of Angelman syndrome, this loss is due to inactivity of the maternal 15q11-q13 encoded UBE3A gene in the brain by either chromosomal deletion or mutation. In cases of Prader-Willi syndrome, there is a partial or complete deletion of this region from the paternal copy of chromosome 15. Tay-Sachs disease is a lethal disorder associated with mutations of the HEXA gene, which is encoded by chromosome 15. Marfan syndrome is associated with chromosome 15 through the FBN1 gene.
Numero del catalogo: BOSSBS-8575R-CY3
UOM: 1 * 100 µl
Proveedor: Bioss


Descripción: Anti-PAIP1 Rabbit Monoclonal Antibody [clone: EPR13258(B)]
Numero del catalogo: ABCAAB249864-100
UOM: 1 * 100 µG
Proveedor: Abcam


Descripción: Anti-PAIP1 Rabbit Polyclonal Antibody (Biotin)
Numero del catalogo: USBI039619-BIOTIN
UOM: 1 * 200 µl
Proveedor: US Biological


Descripción: FSIP1 is a 581 amino acid protein that is expressed in airway epithelium. A member of the FSIP1 family, FSIP1 is encoded by a gene that maps to human chromosome 15q14 and mouse chromosome 2 E5. Encoding more than 700 genes, chromosome 15 is made up of approximately 106 million base pairs and is about 3% of the human genome. Angelman and Prader-Willi syndromes are associated with loss of function or deletion of genes in the 15q11-q13 region. In the case of Angelman syndrome, this loss is due to inactivity of the maternal 15q11-q13 encoded UBE3A gene in the brain by either chromosomal deletion or mutation. In cases of Prader-Willi syndrome, there is a partial or complete deletion of this region from the paternal copy of chromosome 15. Tay-Sachs disease is a lethal disorder associated with mutations of the HEXA gene, which is encoded by chromosome 15. Marfan syndrome is associated with chromosome 15 through the FBN1 gene.
Numero del catalogo: BOSSBS-8575R-CY7
UOM: 1 * 100 µl
Proveedor: Bioss


Descripción: Human FSIP1 ELISA kit is a 90 minutes sandwich Enzyme-Linked Immunosorbent Assay (sELISA) designed for the <i><i>in vitro</i></i> quantitative determination of human FSIP1 in serum, plasma, and other biological fluids.
Numero del catalogo: ANTIA310289-96
UOM: 1 * 96 Tests
Proveedor: ANTIBODIES.COM

New Product


Descripción: Anti-PAIP1 Rabbit Polyclonal Antibody (PE (Phycoerythrin))
Numero del catalogo: USBI039619-PE
UOM: 1 * 200 µl
Proveedor: US Biological


Descripción: Anti-PAIP1 Mouse Polyclonal Antibody
Numero del catalogo: ABNOH00010605-A01
UOM: 1 * 50 µl
Proveedor: Abnova


Descripción: Anti-PAIP1 Rabbit Polyclonal Antibody
Numero del catalogo: PRSI19-985
UOM: 1 * 50 µl
Proveedor: ProSci Inc.

New Product


Descripción: Anti-PAIP1 Rabbit Polyclonal Antibody (APC (Allophycocyanin))
Numero del catalogo: USBI039619-APC
UOM: 1 * 200 µl
Proveedor: US Biological


Descripción: Rabbit polyclonal antibody raised against recombinant FSIP1.
Numero del catalogo: ABNOPAB23733
UOM: 1 * 100 µl
Proveedor: Abnova


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