Esta buscando: psip1

Numero del catalogo: (USBI039619-FITC)

Proveedor: US Biological

Descripción: Anti-PAIP1 Rabbit Polyclonal Antibody (FITC (Fluorescein Isothiocyanate))

UOM: 1 * 200 µl

Promoción

Numero del catalogo: (BOSSBS-8575R-A488)

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.

UOM: 1 * 100 µl

Promoción

Numero del catalogo: (BOSSBS-8575R-A350)

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.

UOM: 1 * 100 µl

Promoción

Numero del catalogo: (BOSSBS-8575R-A555)

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.

UOM: 1 * 100 µl

Promoción

Numero del catalogo: (BOSSBS-8575R-A647)

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.

UOM: 1 * 100 µl

Promoción

Numero del catalogo: (ANTIA90965-100)

Proveedor: ANTIBODIES.COM

Descripción: Anti-FSIP1 Rabbit Polyclonal Antibody

UOM: 1 * 100 µl

New Product Promoción

Numero del catalogo: (ABNOPAB23733)

Proveedor: Abnova

Descripción: Rabbit polyclonal antibody raised against recombinant FSIP1.

UOM: 1 * 100 µl

Promoción

Proveedor: Biorbyt

Descripción: Anti-FSIP1 Rabbit Polyclonal Antibody

Numero del catalogo: (PRSI60-273)

Proveedor: ProSci Inc.

Descripción: For WB starting dilution is: 1:1000.

UOM: 1 * 400 µl

New Product Promoción

Numero del catalogo: (PRSI29-379)

Proveedor: ProSci Inc.

Descripción: PAIP1 interacts with poly (A)-binding protein and with the cap-binding complex eIF4A. It is involved in translational initiation and protein biosynthesis. Overexpression of this gene in COS7 cells stimulates translation.The protein encoded by this gene interacts with poly (A)-binding protein and with the cap-binding complex eIF4A. It is involved in translational initiation and protein biosynthesis. Overexpression of this gene in COS7 cells stimulates translation. Alternative splicing occurs at this locus and three transcript variants encoding three distinct isoforms have been identified.The protein encoded by this gene interacts with poly (A)-binding protein and with the cap-binding complex eIF4A. It is involved in translational initiation and protein biosynthesis. Overexpression of this gene in COS7 cells stimulates translation. Alternative splicing occurs at this locus and three transcript variants encoding three distinct isoforms have been identified.

UOM: 1 * 50 µG

Promoción

Numero del catalogo: (ANTIA15067-100)

Proveedor: ANTIBODIES.COM

Descripción: Anti-PAIP1 Rabbit Polyclonal Antibody

UOM: 1 * 100 µl

New Product Promoción

Numero del catalogo: (PRSI26-736)

Proveedor: ProSci Inc.

Descripción: The exact functions of FSIP1 remain unknown.

UOM: 1 * 50 µG

Promoción

Numero del catalogo: (PRSI29-380)

Proveedor: ProSci Inc.

Descripción: PAIP1 interacts with poly (A)-binding protein and with the cap-binding complex eIF4A. It is involved in translational initiation and protein biosynthesis. Overexpression of this gene in COS7 cells stimulates translation.The protein encoded by this gene interacts with poly (A)-binding protein and with the cap-binding complex eIF4A. It is involved in translational initiation and protein biosynthesis. Overexpression of this gene in COS7 cells stimulates translation. Alternative splicing occurs at this locus and three transcript variants encoding three distinct isoforms have been identified.

UOM: 1 * 100 µG

Promoción

Numero del catalogo: (USBI032117-PE)

Proveedor: US Biological

Descripción: Anti-ASAP1 Rabbit Polyclonal Antibody (PE (Phycoerythrin))

UOM: 1 * 200 µl

Promoción

Numero del catalogo: (USBI039620-APC)

Proveedor: US Biological

Descripción: Anti-PAIP2 Rabbit Polyclonal Antibody (APC (Allophycocyanin))

UOM: 1 * 200 µl

Promoción

Numero del catalogo: (USBI032117)

Proveedor: US Biological

Descripción: Anti-ASAP1 Rabbit Polyclonal Antibody

UOM: 1 * 200 µl

Promoción