PHD Finger Protein 20-Like Protein 1 (PHF20L1) Antibody

Este producto es parte de PHF - PHD finger protein
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292.5€ (80 µl)

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935106861
info@markelab.com
name
PHD Finger Protein 20-Like Protein 1 (PHF20L1) Antibody
category
Primary Antibodies
provider
Abbexa
reference
abx029734
tested applications
ELISA, WB

Description

PHF20L1 (PHD finger protein 20-like 1) is a 554 amino acid protein that contains two tudor domains and is expressed as multiple alternatively spliced isoforms.

Documents del producto

Instrucciones
Data sheet
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Product specifications

Category
Primary Antibodies
Immunogen Target
PHD Finger Protein 20-Like Protein 1 (PHF20L1)
Host
Rabbit
Reactivity
Human
Recommended Dilution
WB: 1/1000. Optimal dilutions/concentrations should be determined by the end user.
Clonality
Polyclonal
Conjugation
Unconjugated
Isotype
IgG
Purification
Purified through a protein A column, followed by peptide affinity purification.
Size 1
80 µl
Size 2
400 µl
Form
Liquid
Tested Applications
ELISA, WB
Buffer
PBS containing 0.09% sodium azide.
Availability
Shipped within 5-10 working days.
Storage
Aliquot and store at -20°C. Avoid repeated freeze/thaw cycles.
Dry Ice
No
UniProt ID
A8MW92
Alias
PHF20L1,CGI-72, CGI-72,TDRD20B,URLC1
Background
Antibody anti-PHF20L1
Status
RUO

Descripción

PHF20L1 is a chromatin-binding protein with a PHD finger domain that recognizes methylated histones, particularly H3K4me3, and contributes to transcriptional regulation and chromatin organization. It functions as a transcriptional co-activator or repressor depending on the cellular context and modulates gene expression programs during development and proliferation. PHF20L1 is associated with the regulation of pluripotency, differentiation, and DNA repair, where it stabilizes chromatin architecture and facilitates the recruitment of histone-modifying complexes. It is widely expressed in proliferative and stem cell-rich tissues, playing roles in maintaining genomic stability and epigenetic regulation. Dysregulation of PHF20L1 has been implicated in cancers and neurodevelopmental disorders due to impaired gene regulation and histone recognition. Knockdown studies reveal defects in gene expression, reduced chromatin stability, and impaired cellular differentiation, underscoring its role in transcriptional control and epigenetic regulation.

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