Antibody data
- Antibody Data
 - Antigen structure
 - References [3]
 - Comments [0]
 - Validations
 - Western blot [1]
 
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Validation data
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- Product number
 - A00201-2 - Provider product page

 - Provider
 - Boster Biological Technology
 - Product name
 - Anti-PINK1 Antibody Picoband™
 - Antibody type
 - Polyclonal
 - Description
 - Rabbit IgG polyclonal antibody for PINK1 detection. Tested with WB, ICC/IF, FCM, Direct ELISA in Human.
 - Reactivity
 - Human
 - Host
 - Rabbit
 - Vial size
 - 100μg/vial
 - Concentration
 - Add 0.2ml of distilled water will yield a concentration of 500ug/ml.
 - Storage
 - At -20°C for one year. After reconstitution, at 4°C for one month. It can also be aliquoted and stored frozen at -20°C for a longer time. Avoid repeated freezing and thawing.
 - Handling
 - Add 0.2ml of distilled water will yield a concentration of 500ug/ml.
 
Submitted references		Atmospheric fine particulate matter (PM(2.5)) induces pulmonary fibrosis by regulating different cell fates via autophagy.
				
Study on the neuroprotective effect of Zhimu-Huangbo extract on mitochondrial dysfunction in HT22 cells induced by D-galactose by promoting mitochondrial autophagy.
				
Robust intervention for oxidative stress-induced injury in periodontitis via controllably released nanoparticles that regulate the ROS-PINK1-Parkin pathway.
				
		
	
			Liu B, Han Y, Ye Y, Wei X, Li G, Jiang W
The Science of the total environment 2024 May 1;923:171396
		The Science of the total environment 2024 May 1;923:171396
Study on the neuroprotective effect of Zhimu-Huangbo extract on mitochondrial dysfunction in HT22 cells induced by D-galactose by promoting mitochondrial autophagy.
			Xue A, Zhao D, Zhao C, Li X, Yang M, Zhao H, Zhao C, Lei X, Wu J, Zhang N
Journal of ethnopharmacology 2024 Jan 10;318(Pt B):117012
		Journal of ethnopharmacology 2024 Jan 10;318(Pt B):117012
Robust intervention for oxidative stress-induced injury in periodontitis via controllably released nanoparticles that regulate the ROS-PINK1-Parkin pathway.
			Li X, Zhao Y, Peng H, Gu D, Liu C, Ren S, Miao L
Frontiers in bioengineering and biotechnology 2022;10:1081977
		Frontiers in bioengineering and biotechnology 2022;10:1081977
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					Supportive validation
					
									
				
		- Submitted by
 - Boster Biological Technology (provider)
 - Main image
 
- Experimental details
 - Western blot analysis of PINK1 using anti-PINK1 antibody (A00201-2). Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 50ug of sample under reducing conditions. Lane 1: human A431 whole cell lysates, Lane 2: human HELA whole cell lysates, Lane 3: human HEPG2 whole cell lysates. After Electrophoresis, proteins were transferred to a Nitrocellulose membrane at 150mA for 50-90 minutes. Blocked the membrane with 5% Non-fat Milk/ TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-PINK1antigen affinity purified polyclonal antibody (Catalog # A00201-2) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for PINK1 at approximately 64KD. The expected band size for PINK1 is at 64KD.
 - Additional image
 