PHD Finger Protein 13 (PHF13) Antibody

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

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935106861
info@markelab.com
name
PHD Finger Protein 13 (PHF13) Antibody
category
Primary Antibodies
provider
Abbexa
reference
abx036836
tested applications
ELISA, WB

Description

Rabbit Polyclonal against the PHF13 protein.

Documents del producto

Instrucciones
Data sheet
Descargar

Product specifications

Category
Primary Antibodies
Immunogen Target
PHD Finger Protein 13 (PHF13)
Host
Rabbit
Reactivity
Human
Recommended Dilution
ELISA: 1/20000 - 1/80000, WB: 1/500 - 1/2000. 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
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
PHF12, KIAA1523,PHD factor 1,PF1
Background
Antibody anti-PHF13
Status
RUO
Note
Concentration: Lyophilized form: Not applicable.  After reconstitution: 1 mg/ml. - 

Descripción

PHF13 is a chromatin-binding protein with a PHD finger domain that recognizes methylated histone residues, particularly H3K4me3, to regulate transcriptional activation and chromatin accessibility. It functions as a transcriptional co-activator, recruiting chromatin remodelers and transcription machinery to active gene loci. PHF13 is involved in processes such as DNA repair, cellular differentiation, and the regulation of pluripotency genes in embryonic stem cells. It is expressed in various tissues, including hematopoietic and neural lineages, where it modulates lineage-specific gene expression programs. Dysregulation of PHF13 has been associated with impaired DNA damage response, developmental defects, and tumorigenesis, where altered chromatin dynamics affect cellular proliferation and survival. Knockout studies demonstrate reduced transcriptional activation, defective chromatin remodeling, and impaired cellular differentiation, underscoring its role in maintaining transcriptional fidelity and chromatin structure during development and stress responses.

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