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

Este producto es parte de PHF - PHD finger protein
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357.5€ (100 µg)

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935106861
info@markelab.com
name
PHD Finger Protein 20-Like Protein 1 (PHF20L1) Antibody
category
Primary Antibodies
provider
Abbexa
reference
abx036932
tested applications
ELISA, WB, IHC

Description

Rabbit Polyclonal against the PHF20L1 protein.

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
ELISA: 1/20000 - 1/80000, WB: 1/500 - 1/2000, IHC: 1/100 - 1/200. Optimal dilutions/concentrations should be determined by the end user.
Clonality
Polyclonal
Conjugation
Unconjugated
Isotype
IgG
Purification
Purified by antigen affinity column chromatography.
Size 1
100 µg
Size 2
1 mg
Form
Lyophilized
Tested Applications
ELISA, WB, IHC
Buffer
Prior to lyophilization: 1% BSA and 0.02% NaN3.
Availability
Shipped within 7-15 working days.
Storage
Store at -20 °C. Avoid repeated freeze/thaw cycles.
Dry Ice
No
Alias
PHF20L1,CGI-72, CGI-72,TDRD20B,URLC1
Background
Antibody anti-PHF20L1
Status
RUO
Note
Concentration: Lyophilized form: Not applicable.  After reconstitution: 1 mg/ml. -

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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