PAX6 Mouse Monoclonal Antibody

PAX6 Mouse Monoclonal Antibody

Cat: AMM80859
Size:50μL Price:$168
Size:100μL Price:$300
Application:ELISA,FC

Reactivity:Human
Conjugate:Unconjugated
Optional conjugates: Biotin, FITC (free of charge).
See other 26 conjugates.

Gene Name:PAX6
Category: Mouse Monoclonal Antibody Tags:

Summary

Production Name

PAX6 Mouse Monoclonal Antibody

Description

Mouse monoclonal Antibody

Host

Mouse

Application

ELISA,FC

Reactivity

Human

 

Performance

Conjugation

Unconjugated

Modification

Unmodified

Isotype

Mouse IgG1

Clonality

Monoclonal

Form

Liquid

Storage

Store at 4°C short term. Aliquot and store at -20°C long term. Avoid freeze/thaw cycles.

Buffer

Purified antibody in PBS with 0.05% sodium azide.

Purification

Affinity Purification

 

Immunogen

Gene Name

PAX6

Alternative Names

AN; AN2; MGDA; WAGR; D11S812E; MGC17209; PAX6

Gene ID

5080

SwissProt ID

P26367

 

Application

Dilution Ratio

ELISA 1:5000-1:20000,FC 1:200-1:400

Molecular Weight

46kDa

 

Background

Transcription factor with important functions in the development of the eye, nose, central nervous system and pancreas. Required for the differentiation of pancreatic islet alpha cells .PAX6 is the most researched of the PAX genes and appears throughout the literature as a "master control" gene for the development of eyes and other sensory organs, certain neural and epidermal tissues as well as other homologous structures, usually derived from ectodermal tissues. This transcription factor is most famous for its use in the interspecifically induced expression of ectopic eyes and is of medical importance because heterozygous mutants produce a wide spectrum of ocular defects such as Aniridia in humans. This gene encodes paired box gene 6, one of many human homologues of the Drosophila melanogaster gene prd. In addition to the hallmark feature of this gene family, a conserved paired box domain, the encoded protein also contains a homeo box domain. Both domains are known to bind DNA, and function as regulators of gene transcription. This gene is expressed in the developing nervous system, and in developing eyes. Mutations in this gene are known to cause aniridia as well as Peter's anomaly, both ocular diseases.

 

Research Area

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