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ALX4 Mouse anti-Human, Clone: OTI1F2, Invitrogen™

Mouse Monoclonal Antibody

Manufacturer:  Invitrogen MA526062

Catalog No. PIMA526062


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Description

Description

This gene encodes a paired-like homeodomain transcription factor expressed in the mesenchyme of developing bones, limbs, hair, teeth, and mammary tissue. Mutations in this gene cause parietal foramina 2 (PFM2); an autosomal domit disease characterized by deficient ossification of the parietal bones. Mutations in this gene also cause a form of frontonasal dysplasia with alopecia and hypogonadism; suggesting a role for this gene in craniofacial development, mesenchymal-epithelial communication, and hair follicle development. Deletion of a segment of chromosome 11 containing this gene, del(11)(p11p12), causes Potocki-Shaffer syndrome (PSS); a syndrome characterized by craniofacial anomalies, mental retardation, multiple exostoses, and genital abnormalities in males. In mouse, this gene has been shown to use dual translation initiation sites located 16 codons apart.
Specifications

Specifications

ALX4
Monoclonal
1 mg/mL
PBS with 1% BSA, 50% glycerol and 0.02% sodium azide; pH 7.3
Q9H161
FND2, aristaless-like homeobox 4, homeobox protein aristaless-like 4, homeodomain transcription factor ALX4
Mouse
IgG1
100 μL
-20° C, Avoid Freeze/Thaw Cycles
Primary
60529
Immunohistochemistry (Paraffin), Western Blot
OTI1F2
Unconjugated
ALX4
Liquid
ALX4
Full length human recombit protein of ALX4 produced in HEK293T cell
Affinity Chromatography
RUO
Antibody
Monoclonal
Human
Documents
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