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PAX3 Recombinant monoclonal antibody, PBS Only

PAX3 Uni-rAb® Recombinant Antibody for WB, Indirect ELISA

Cat No. 87980-1-PBS
Clone No.253577F9

Host / Isotype

Rabbit / IgG

Reactivity

human, mouse

Applications

WB, Indirect ELISA

CDHS, paired box 3, Paired box protein Pax 3, Paired box protein Pax-3, PAX-3

Formulation:  PBS Only
Conjugate:  Unconjugated
Size/Concentration: 

-/ -

Freight/Packing: -

Quantity

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Product Information

87980-1-PBS targets PAX3 in WB, Indirect ELISA applications and shows reactivity with human, mouse samples.

Tested Reactivity human, mouse
Host / Isotype Rabbit / IgG
Class Recombinant
Type Antibody
Immunogen

CatNo: Ag16021

Product name: Recombinant human PAX3 protein

Source: e coli.-derived, PGEX-4T

Tag: GST

Domain: 341-426 aa of BC101301

Sequence: QSTIPSNPDSSSAYCLPSTRHGFSSYTDSFVPPSGPSNPMNPTIGNGLSPQVMGLLTNHGGVPHQPQTDYALSPLTGGLEPTTTVS

Predict reactive species
Full Name paired box 3
Calculated Molecular Weight 484 aa, 53 kDa
Observed Molecular Weight53-56 kDa
GenBank Accession NumberBC101301
Gene Symbol PAX3
Gene ID (NCBI) 5077
RRIDAB_3745845
Conjugate Unconjugated
FormLiquid
Purification MethodProtein A purification
UNIPROT IDP23760
Storage Buffer PBS only, pH 7.3.
Storage ConditionsStore at -80°C.

Background Information

PAX3, a transcription factor and multifunctional regulatory protein, is normally expressed during embryonic development. In the nervous system, PAX3 is involved in neural tube closure, neural crest development, and peripheral neuron differentiation. In the present study, PAX3 was reported as a novel regulator of GFAP transcription, and the overexpression and suppression of PAX3 could inhibit and promote NSC differentiation, respectively. In muscle development, PAX3 ensures the survival of myogenic progenitor cells with Pax3-expressing progenitors giving rise to both skeletal and smooth muscle cells. PAX3 also has a well-established role in the development of melanocytes during embryogenesis, and has recently been characterized as a molecular switch in the mature melanocyte. Mutations in PAX3 can cause Waardenburg syndrome.

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