产品名称
p16INK4a Recombinant Rabbit Monoclonal Antibody [PSH15-40] - BSA and Azide free
抗体类型
Recombinant Rabbit monoclonal Antibody
靶点分子量
Predicted band size: 18 kDa
阳性对照
A20 cell lysate, MEF cell lysate, mouse spleen tissue.
Tested
已验证(内部验证通过)
Published
文献已报道(未内部验证,但有文献支持)
Predicted
预测可反应(基于高同源性)
Not recommended
不推荐(内部验证未通过)
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WB |
IHC-P |
FC |
IF-Cell |
| human |
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| mouse |
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| rat |
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存放说明
Store at 2-8℃. Avoid freeze.
纯化方式
Protein A affinity purified.
功能
p16 (also known as p16INK4a, cyclin-dependent kinase inhibitor 2A, CDKN2A, multiple tumor suppressor 1 and numerous other synonyms), is a protein that slows cell division by slowing the progression of the cell cycle from the G1 phase to the S phase, thereby acting as a tumor suppressor. It is encoded by the CDKN2A gene. A deletion (the omission of a part of the DNA sequence during replication) in this gene can result in insufficient or non-functional p16, accelerating the cell cycle and resulting in many types of cancer. p16 can be used as a biomarker to improve the histological diagnostic accuracy of grade 3 cervical intraepithelial neoplasia (CIN). p16 is also implicated in the prevention of melanoma, oropharyngeal squamous cell carcinoma, cervical cancer, vulvar cancer and esophageal cancer. p16 was discovered in 1993. It is a protein with 148 amino acids and a molecular weight of 16 kDa that comprises four ankyrin repeats. The name of p16 is derived from its molecular weight, and the alternative name p16INK4a refers to its role in inhibiting cyclin-dependent kinase CDK4.
背景文献
1. Safwan-Zaiter H et al. P16INK4A-More Than a Senescence Marker. Life (Basel). 2022 Aug
2. Shi J et al. P16ink4a overexpression ameliorates cardiac remodeling of mouse following myocardial infarction via CDK4/pRb pathway. Biochem Biophys Res Commun. 2022 Mar
别名
CCM2 antibody
CDK4 inhibitor p16 INK4 antibody
CDK4I antibody
CDKN2 antibody
CDKN2A antibody
Cell cycle negative regulator beta antibody
CMM2 antibody
Cyclin dependent kinase 4 inhibitor A antibody
Cyclin dependent kinase inhibitor 2A (melanoma p16 inhibits CDK4) antibody
Cyclin Dependent Kinase Inhibitor 2A antibody
展开
CCM2 antibody
CDK4 inhibitor p16 INK4 antibody
CDK4I antibody
CDKN2 antibody
CDKN2A antibody
Cell cycle negative regulator beta antibody
CMM2 antibody
Cyclin dependent kinase 4 inhibitor A antibody
Cyclin dependent kinase inhibitor 2A (melanoma p16 inhibits CDK4) antibody
Cyclin Dependent Kinase Inhibitor 2A antibody
Cyclin dependent kinase inhibitor 2A isoform 4 antibody
Cyclin dependent kinase inhibitor 2A isoforms 1/2/3 antibody
Cyclin dependent kinase inhibitor p16 antibody
INK4 antibody
INK4A antibody
MLM antibody
MTS1 antibody
Multiple tumor suppressor 1 antibody
p14 antibody
p16 antibody
P16INK4 antibody
p16INK4a antibody
p19 antibody
p19Arf antibody
TP16 antibody
折叠
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☑ Relative expression (RE)
This data was developed using HA723746, the same antibody clone in a different buffer formulation.
Western blot analysis of p16INK4a on different lysates with Rabbit anti-p16INK4a antibody (HA723746) at 1/2,000 dilution.
Lane 1: A20 cell lysate
Lane 2: NIH/3T3 cell lysate (negative)
Lane 3: MEF cell lysate
Lysates/proteins at 20 µg/Lane.
Predicted band size: 18 kDa
Observed band size: 16 kDa
Exposure time: 1 minute 50 seconds; ECL: K1801;
4-20% SDS-PAGE gel.
Proteins were transferred to a PVDF membrane and blocked with 5% NFDM/TBST for 1 hour at room temperature. The primary antibody (HA723746) at 1/2,000 dilution was used in primary antibody dilution (K1803) at 4℃ overnight. Goat Anti-Rabbit IgG - HRP Secondary Antibody (HA1001) at 1/50,000 dilution was used for 1 hour at room temperature.
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This data was developed using HA723746, the same antibody clone in a different buffer formulation.
Immunohistochemical analysis of paraffin-embedded mouse spleen tissue with Rabbit anti-p16INK4a antibody (HA723746) at 1/200 dilution.
The section was pre-treated using heat mediated antigen retrieval with Tris-EDTA buffer (pH 9.0) for 20 minutes. The tissues were blocked in 1% BSA for 20 minutes at room temperature, washed with ddH2O and PBS, and then probed with the primary antibody (HA723746) at 1/200 dilution for 1 hour at room temperature. The detection was performed using an HRP conjugated compact polymer system. DAB was used as the chromogen. Tissues were counterstained with hematoxylin and mounted with DPX.
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This data was developed using HA723746, the same antibody clone in a different buffer formulation.
p16INK4a was immunoprecipitated from 0.2 mg MEF cell lysate with HA723746 at 2 µg/10 µl beads. Western blot was performed from the immunoprecipitate using HA723746 at 1/1,000 dilution. HRP Conjugated Anti-Rabbit IgG for IP Nano-secondary antibody at 1/5,000 dilution was used for 1 hour at room temperature.
Lane 1: MEF cell lysate (input)
Lane 2: HA723746 IP in MEF cell lysate
Lane 3: Rabbit IgG instead of HA723746 in MEF cell lysate
Blocking/Dilution buffer: primary antibody dilution (K1803)
Exposure time: 3 minutes; ECL: K1801
请注意: All products are "FOR RESEARCH USE ONLY AND ARE NOT INTENDED FOR DIAGNOSTIC OR THERAPEUTIC USE"