PHD Finger Protein 21B (PHF21B) Antibody

Este producto es parte de PHF - PHD finger protein
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195€ (20 µl)

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935106861
info@markelab.com
name
PHD Finger Protein 21B (PHF21B) Antibody
category
Primary Antibodies
provider
Abbexa
reference
abx006556
tested applications
ELISA, WB

Description

PHF21B Antibody is a Rabbit Polyclonal Antibody against PHF21B.

Documents del producto

Instrucciones
Data sheet
Descargar

Product specifications

Category
Primary Antibodies
Immunogen Target
PHD Finger Protein 21B (PHF21B)
Host
Rabbit
Reactivity
Human, Mouse, Rat
Recommended Dilution
ELISA: 1 µg/ml, WB: 1/500 - 1/2000. Optimal dilutions/concentrations should be determined by the end user.
Clonality
Polyclonal
Conjugation
Unconjugated
Isotype
IgG
Purification
Purified by affinity chromatography.
Size 1
20 µl
Size 2
100 µl
Size 3
2 × 100 µl
Form
Liquid
Tested Applications
ELISA, WB
Buffer
PBS, pH 7.3, containing 0.02% sodium azide, 50% glycerol.
Availability
Shipped within 5-10 working days.
Storage
Aliquot and store at -20°C. Avoid repeated freeze/thaw cycles.
Dry Ice
No
UniProt ID
Q96EK2
Gene ID
112885
NCBI Accession
NP_612424.1
Alias
PHF21B,KIAA1661,BHC80L,PHF4
Background
Antibody anti-PHF21B
Status
RUO
Note
Concentration: > 0.2 mg/ml -

Descripción

PHF21B is a chromatin-binding protein containing a PHD domain, which recognizes and interacts with methylated histones to regulate transcriptional activation or repression. It is involved in chromatin remodeling and modulating gene expression programs linked to cellular proliferation, differentiation, and tumor suppression. PHF21B is expressed in epithelial tissues and immune cells, where it controls pathways involved in cell cycle progression and immune responses. Emerging evidence suggests that PHF21B plays a role in tumor suppression by stabilizing chromatin architecture and regulating oncogene expression. Dysregulation of PHF21B has been implicated in cancers, including breast and colorectal cancer, where its loss of function leads to uncontrolled cell proliferation and genomic instability. Functional studies demonstrate defects in transcriptional repression, impaired chromatin organization, and increased oncogenic signaling, underscoring its role as a critical regulator of epigenetic control and tumor suppression.

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