|Application ||WB, E|
|Other Accession||Q8AVR4, Q6NX65, Q8VE70, Q5ZIV5, Q6PHH3, NP_009148.2|
|Predicted||Zebrafish, Chicken, Mouse, Rat, Xenopus|
|Calculated MW||24702 Da|
|Antigen Region||96-124 aa|
|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.|
|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.|
|Storage||Maintain refrigerated at 2-8°C for up to 2 weeks. For long term storage store at -20°C in small aliquots to prevent freeze-thaw cycles.|
|Precautions||PDCD10 Antibody (Center) is for research use only and not for use in diagnostic or therapeutic procedures.|
|Function||Promotes cell proliferation. Modulates apoptotic pathways. Increases mitogen-activated protein kinase activity and STK26 activity. Important for cell migration, and for normal structure and assembly of the Golgi complex. Important for KDR/VEGFR2 signaling. Increases the stability of KDR/VEGFR2 and prevents its breakdown. Required for normal cardiovascular development. Required for normal angiogenesis, vasculogenesis and hematopoiesis during embryonic development (By similarity).|
|Cellular Location||Cytoplasm. Golgi apparatus membrane; Peripheral membrane protein; Cytoplasmic side. Cell membrane; Peripheral membrane protein; Cytoplasmic side. Note=Partially co- localizes with endogenous PXN at the leading edges of migrating cells|
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Provided below are standard protocols that you may find useful for product applications.
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].
Lauenborg, B., et al. APMIS 118(10):719-728(2010)
Shimada, M., et al. Hum. Genet. 128(4):433-441(2010)
Ding, J., et al. Biochem. Biophys. Res. Commun. 399(4):587-592(2010)
Zheng, X., et al. J. Clin. Invest. 120(8):2795-2804(2010)
Dibble, C.F., et al. PLoS ONE 5 (7), E11740 (2010) :
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