PDCD10 polyclonal (Center), anti-human
€0.00
In stock
SKU
AC-AP17989c
Catalog Number: AC-AP17989c
Size: 80 µl, 400 µl
Isotype: Rabbit IgG
Clone Name: RB21118
Applications: WB
Datasheet
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Size: 80 µl, 400 µl
Isotype: Rabbit IgG
Clone Name: RB21118
Applications: WB
Datasheet
Request Information
Background:
This gene encodes an evolutionarily conserved protein associated with cell apoptosis. The protein interacts with the serine/threonine protein kinase MST4 to modulate the extracellular signal-regulated kinase (ERK) pathway. It also interacts with and is phosphoryated by serine/threonine kinase 25, and is thought to function in a signaling pathway essential for vascular developent. Mutations in this gene are one cause of cerebral cavernous malformations, which are vascular malformations that cause seizures and cerebral hemorrhages. Multiple alternatively spliced variants, encoding the same protein, have been identified. [provided by RefSeq].
Other Names:
Programmed cell death protein 10, Cerebral cavernous malformations 3 protein, TF-1 cell apoptosis-related protein 15, PDCD10, CCM3, TFAR15
Target/Specificity:
This PDCD10 antibody is generated from rabbits immunized with a KLH conjugated synthetic peptide between 96-124 amino acids from the Central region of human PDCD10.
Antigen Region:
96-124
Antigen Type: Synthetic Peptide
Gene Name: PDCD10 (HGNC:8761)
Gene ID: 11235
Primary Accession: Q9BUL8
NCBI Accession: NP_009148.2;NP_665858.1;NP_665859.1
Other Accession: Q8AVR4; Q6NX65; Q8VE70; Q5ZIV5; Q6PHH3; NP_009148.2
Format: Purified polyclonal antibody supplied in PBS with 0.09% (W/V) sodium azide. This antibody is purified through a protein A column, followed by peptide affinity purification.
This gene encodes an evolutionarily conserved protein associated with cell apoptosis. The protein interacts with the serine/threonine protein kinase MST4 to modulate the extracellular signal-regulated kinase (ERK) pathway. It also interacts with and is phosphoryated by serine/threonine kinase 25, and is thought to function in a signaling pathway essential for vascular developent. Mutations in this gene are one cause of cerebral cavernous malformations, which are vascular malformations that cause seizures and cerebral hemorrhages. Multiple alternatively spliced variants, encoding the same protein, have been identified. [provided by RefSeq].
Other Names:
Programmed cell death protein 10, Cerebral cavernous malformations 3 protein, TF-1 cell apoptosis-related protein 15, PDCD10, CCM3, TFAR15
Target/Specificity:
This PDCD10 antibody is generated from rabbits immunized with a KLH conjugated synthetic peptide between 96-124 amino acids from the Central region of human PDCD10.
Antigen Region:
96-124
Antigen Type: Synthetic Peptide
Gene Name: PDCD10 (HGNC:8761)
Gene ID: 11235
Primary Accession: Q9BUL8
NCBI Accession: NP_009148.2;NP_665858.1;NP_665859.1
Other Accession: Q8AVR4; Q6NX65; Q8VE70; Q5ZIV5; Q6PHH3; NP_009148.2
Format: Purified polyclonal antibody supplied in PBS with 0.09% (W/V) sodium azide. This antibody is purified through a protein A column, followed by peptide affinity purification.
| Is Featured? | No |
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