DNA-binding protein SATB2 (SATB2) Antibody (FITC)

Este producto es parte de SATB homeobox
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260€ (50 µl)

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935106861
info@markelab.com
name
DNA-binding protein SATB2 (SATB2) Antibody (FITC)
category
Primary Antibodies
provider
Abbexa
reference
abx349643

Description

DNA-binding protein SATB2 (SATB2) Antibody (FITC) is a Rabbit Polyclonal antibody conjugated to FITC for the detection of Human SATB2.

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Data sheet
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Product specifications

CategoryPrimary Antibodies
Immunogen TargetDNA-binding protein SATB2 (SATB2)
HostRabbit
ReactivityHuman
Recommended DilutionOptimal dilutions/concentrations should be determined by the end user.
ClonalityPolyclonal
ConjugationFITC
IsotypeIgG
Purity> 95%
PurificationPurified by antigen affinity chromatography.
Size 150 µl
Size 2100 µl
Size 3200 µl
Size 41 ml
FormLiquid
Buffer0.01 M PBS, pH 7.4, 0.03% Proclin-300 and 50% glycerol.
AvailabilityShipped within 5-10 working days.
StorageAliquot and store at -20°C. Avoid repeated freeze/thaw cycles.
Dry IceNo
UniProt IDQ9UPW6
Gene ID23314
OMIM119540
AliasC2DELq32q33,DEL2Q32Q33,GLSS,Special AT-rich sequence-binding protein 2,DNA-binding protein SATB2
BackgroundAntibody anti-SATB2
StatusRUO

Descripción

SATB homeobox 2 (SATB2) is a transcription factor that plays a crucial role in chromatin organization, gene regulation, and cellular differentiation SATB2 is involved in the regulation of skeletal development, neural differentiation, and craniofacial patterning, particularly during embryogenesis It functions by binding to specific DNA sequences and organizing chromatin into loops, facilitating the regulation of gene expression in a spatially organized manner SATB2 is highly expressed in osteoblasts and neurons, where it influences the expression of genes involved in bone formation and synaptic plasticity Mutations in SATB2 lead to developmental disorders such as SATB2-associated syndrome, which is characterized by intellectual disability, speech delays, and craniofacial abnormalities SATB2 also plays a role in cancer, where it can modulate tumor progression and metastasis through its effects on chromatin structure and gene expression Recent studies have highlighted its potential as a therapeutic target for regenerative medicine and in disorders involving disrupted bone and neural development

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