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p16INK4a Recombinant Rabbit Monoclonal Antibody [PSH15-40] - BSA and Azide free

Usd: 649

Specification

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Catalog# HA751555

p16INK4a Recombinant Rabbit Monoclonal Antibody [PSH15-40] - BSA and Azide free

Application

  • WB

  • IHC-P

  • IP

Reactivity

  • Mouse

With BSA and Azide
Conjugation

  • unconjugated

Overview

Product Name

p16INK4a Recombinant Rabbit Monoclonal Antibody [PSH15-40] - BSA and Azide free

Antibody Type

Recombinant Rabbit monoclonal Antibody

Species Reactivity

Mouse

Validated Applications

WB, IHC-P, IP

Molecular Weight

Predicted band size: 18 kDa

Positive Control

A20 cell lysate, MEF cell lysate, mouse spleen tissue.

Conjugation

unconjugated

Clone Number

PSH15-40

Product Features

Form

Liquid

Concentration

1mg/ml

Storage Instructions

Store at +4℃ after thawing. Aliquot store at -20℃. Avoid repeated freeze / thaw cycles.

Storage Buffer

1*PBS (pH7.4).

Isotype

IgG

Purification Method

Protein A affinity purified.

Application Dilution

  • WB

  • 1:2,000

  • IHC-P

  • 1:200

  • IP

  • 1:1,000

Target

Function

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.

Background References

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

Subcellular Location

Cytoplasm, Nucleus.

UNIPROT

SwissProt: P51480 Mouse

Synonyms

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

Expand

Images

  • <span style="font-weight: bold;">☑ Relative expression (RE)</span><br /><br />Western blot analysis of p16INK4a on different lysates with Rabbit anti-p16INK4a antibody (<a href="/products/HA751555" style="font-weight: bold;text-decoration: underline;">HA751555</a>) at 1/2,000 dilution.<br /><br />Lane 1: A20 cell lysate<br />Lane 2: NIH/3T3 cell lysate (negative)<br />Lane 3: MEF cell lysate<br /><br />Lysates/proteins at 20 µg/Lane.<br /><br />Predicted band size: 18 kDa<br />Observed band size: 16 kDa<br /><br />Exposure time: 1 minute 50 seconds; ECL: K1801;<br /><br />4-20% SDS-PAGE gel.<br /><br />Proteins were transferred to a PVDF membrane and blocked with 5% NFDM/TBST for 1 hour at room temperature. The primary antibody (<a href="/products/HA751555" style="font-weight: bold;text-decoration: underline;">HA751555</a>) at 1/2,000 dilution was used in primary antibody dilution (<a href="/products/K1803" style="font-weight: bold;text-decoration: underline;">K1803</a>) at 4℃ overnight. Goat Anti-Rabbit IgG - HRP Secondary Antibody (<a href="/products/HA1001" style="font-weight: bold;text-decoration: underline;">HA1001</a>) at 1/50,000 dilution was used for 1 hour at room temperature.

    ☑ Relative expression (RE)

    Western blot analysis of p16INK4a on different lysates with Rabbit anti-p16INK4a antibody (HA751555) 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 (HA751555) 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.

  • Immunohistochemical analysis of paraffin-embedded mouse spleen tissue with Rabbit anti-p16INK4a antibody (<a href="/products/HA751555" style="font-weight: bold;text-decoration: underline;">HA751555</a>) at 1/200 dilution.<br /><br />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 ddH<sub>2</sub>O and PBS, and then probed with the primary antibody (<a href="/products/HA751555" style="font-weight: bold;text-decoration: underline;">HA751555</a>) 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.

    Immunohistochemical analysis of paraffin-embedded mouse spleen tissue with Rabbit anti-p16INK4a antibody (HA751555) 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 (HA751555) 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.

  • p16INK4a was immunoprecipitated from 0.2 mg MEF cell lysate with <a href="/products/HA751555" style="font-weight: bold;text-decoration: underline;">HA751555</a> at 2 µg/10 µl beads. Western blot was performed from the immunoprecipitate using <a href="/products/HA751555" style="font-weight: bold;text-decoration: underline;">HA751555</a> 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.<br /><br />Lane 1: MEF cell lysate (input)<br />Lane 2: <a href="/products/HA751555" style="font-weight: bold;text-decoration: underline;">HA751555</a> IP in MEF cell lysate<br />Lane 3: Rabbit IgG instead of <a href="/products/HA751555" style="font-weight: bold;text-decoration: underline;">HA751555</a> in MEF cell lysate<br /><br />Blocking/Dilution buffer: primary antibody dilution (<a href="/products/K1803" style="font-weight: bold;text-decoration: underline;">K1803</a>)<br />Exposure time: 3 minutes; ECL: <a href="/products/K1801" style="font-weight: bold;text-decoration: underline;">K1801</a>

    p16INK4a was immunoprecipitated from 0.2 mg MEF cell lysate with HA751555 at 2 µg/10 µl beads. Western blot was performed from the immunoprecipitate using HA751555 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: HA751555 IP in MEF cell lysate
    Lane 3: Rabbit IgG instead of HA751555 in MEF cell lysate

    Blocking/Dilution buffer: primary antibody dilution (K1803)
    Exposure time: 3 minutes; ECL: K1801

Please note: All products are "FOR RESEARCH USE ONLY AND ARE NOT INTENDED FOR DIAGNOSTIC OR THERAPEUTIC USE"