PA5-112229
antibody from Invitrogen Antibodies
		Targeting: PEG10
		
		HB-1, KIAA1051, Mar2, Mart2, MEF3L, RGAG3, RTL2, SIRH1	
	
	
	
	
Antibody data
- Antibody Data
 - Antigen structure
 - References [0]
 - Comments [0]
 - Validations
 - Immunocytochemistry [3]
 - Immunoprecipitation [1]
 - Immunohistochemistry [2]
 - Other assay [1]
 
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- Product number
 - PA5-112229 - Provider product page

 - Provider
 - Invitrogen Antibodies
 - Product name
 - PEG10 Polyclonal Antibody
 - Antibody type
 - Polyclonal
 - Antigen
 - Other
 - Reactivity
 - Human
 - Host
 - Rabbit
 - Isotype
 - IgG
 - Vial size
 - 100 μL
 - Concentration
 - 1 mg/mL
 - Storage
 - Store at 4°C short term. For long term storage, store at -20°C, avoiding freeze/thaw cycles.
 
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					Supportive validation
					
									
				
				- Submitted by
 - Invitrogen Antibodies (provider)
 - Main image
 
- Experimental details
 - Immunocytochemistry-Immunofluorescence analysis of PEG10 in HepG2 cells. Cells were fixed with 4% PFA, permeabilized with 0.1% Triton X-100 in PBS, blocked with 10% serum, and incubated with PEG10 Polyclonal Antibody (Product # PA5-112229) (1:200) at 4°C overnight. Then cells were stained with the Alexa Fluor 488-conjugated Goat Anti-rabbit IgG secondary antibody (green) and counterstained with DAPI (blue). Positive staining was localized to Cytoplasm.
 
- Submitted by
 - Invitrogen Antibodies (provider)
 - Main image
 
- Experimental details
 - Immunocytochemistry-Immunofluorescence analysis of PEG10 in HepG2 cells. Cells were fixed with 4% PFA, permeabilized with 0.1% Triton X-100 in PBS, blocked with 10% serum, and incubated with PEG10 Polyclonal Antibody (Product # PA5-112229) (1:200) at 4°C overnight. Then cells were stained with the Alexa Fluor 488-conjugated Goat Anti-rabbit IgG secondary antibody (green) and counterstained with DAPI (blue). Positive staining was localized to Cytoplasm.
 
- Submitted by
 - Invitrogen Antibodies (provider)
 - Main image
 
- Experimental details
 - Immunocytochemistry-Immunofluorescence analysis of PEG10 in HepG2 cells. Cells were fixed with 4% PFA, permeabilized with 0.1% Triton X-100 in PBS, blocked with 10% serum, and incubated with PEG10 Polyclonal Antibody (Product # PA5-112229) (1:200) at 4°C overnight. Then cells were stained with the Alexa Fluor 488-conjugated Goat Anti-rabbit IgG secondary antibody (green) and counterstained with DAPI (blue). Positive staining was localized to Cytoplasm.
 
							
					Supportive validation
					
									
				
				- Submitted by
 - Invitrogen Antibodies (provider)
 - Main image
 
- Experimental details
 - Immunoprecipitation of PEG10 was performed on (Lane A) 0.5 mg HEK 293 whole cell lysate using 4 µL of PEG10 Polyclonal Antibody (Product # PA5-112229) at a dilution of 1:100, and 60 µg of Immunomagnetic beads Protein A/G. A Goat Anti-Rabbit IgG (H+L)/HRP was used as a secondary antibody at a dilution of 1:10,000. Developed using the ECL technique and performed under reducing conditions. Predicted band size: 30 kDa. Observed band size: 100 kDa.
 
							
					Supportive validation
					
									
				
				- Submitted by
 - Invitrogen Antibodies (provider)
 - Main image
 
- Experimental details
 - Immunohistochemistry analysis of PEG10 in formalin-fixed paraffin embedded sections human adrenal gland tissue sections using PEG10 Polyclonal Antibody (Product # PA5-112229) at a dilution of 1:1000.
 
- Submitted by
 - Invitrogen Antibodies (provider)
 - Main image
 
- Experimental details
 - Immunohistochemistry analysis of PEG10 in formalin-fixed paraffin embedded sections human placenta tissue sections using PEG10 Polyclonal Antibody (Product # PA5-112229) at a dilution of 1:1000.
 
							
					Supportive validation
					
									
				
		- Submitted by
 - Invitrogen Antibodies (provider)
 - Main image
 
- Experimental details
 - Immunoprecipitation of PEG10 was performed on (Lane A) 0.5 mg HEK 293 whole cell lysate using 4 µL of PEG10 Polyclonal Antibody (Product # PA5-112229) at a dilution of 1:100, and 60 µg of Immunomagnetic beads Protein A/G. A Goat Anti-Rabbit IgG (H+L)/HRP was used as a secondary antibody at a dilution of 1:10,000. Developed using the ECL technique and performed under reducing conditions. Predicted band size: 30 kDa. Observed band size: 100 kDa.