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Total Dlx-3 Cell-Based Colorimetric ELISA Kit

-KA3473C

Catalog: KA3473C
Size
Price
Status
Qty.
96well
$330.00
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Main Information
Reactivity

Human, Mouse

Applications

ELISA

Conjugate/Modification


Unmodified

Detailed Information
Storage
2-8°C/6 months
Modification
Unmodified
Detection Method
Colorimetric
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Antigen&Target Information
Gene Name:
DLX3
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Other Name:
Homeobox protein DLX-3
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Database Link:
Organism Gene ID SwissProt
Human 1747; O60479;
Mouse Q64205;
Background:
disease:Defects in DLX3 are a cause of trichodentoosseous syndrome (TDO) [MIM:190320]. TDO is an autosomal dominant syndrome characterized by enamel hypoplasia and hypocalcification with associated strikingly curly hair.,disease:Defects in DLX3 are the cause of amelogenesis imperfecta type 4 (AI4) [MIM:104510]; also known as amelogenesis imperfecta hypomaturation-hypoplastic type with taurodontism. AI4 is an autosomal dominant defect of enamel formation associated with enlarged pulp chambers.,function:Likely to play a regulatory role in the development of the ventral forebrain. May play a role in craniofacial patterning and morphogenesis.,similarity:Belongs to the distal-less homeobox family.,similarity:Contains 1 homeobox DNA-binding domain.,
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Function:
blood vessel development, placenta development, vasculature development, regulation of transcription, DNA-dependent, regulation of transcription, regulation of RNA metabolic process,
show all
Cellular Localization:
Nucleus .
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Catalog: KA3473C
Size
Price
Status
Qty.
96well
$330.00
In stock

0

Add to cart

Collected

Collect

Customized Service

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