Anti-DLX3 Antibody

$99.00$319.00

Reactivity: Human
Applications: ELISA,IHC
Conjugation: Various
Supplier: CUSABIO BIOTECH CO.

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Rabbit Anti-DLX3 Antibody (CSB-PA006954ESR2HU)

Supplier: CUSABIO BIOTECH CO.

Alternative names:

Homeobox protein DLX-3 Antibody,DLX3 Antibody

More alternative names for the antibody
AI4 antibody|Distal less homeo box 3 antibody|DLX 3 antibody|Dlx3 antibody|DLX3 distalless homeobox 3 antibody|DLX3_HUMAN antibody|Homeobox protein DLX 3 antibody|Homeobox protein DLX-3 antibody|Homeobox protein Dlx3 antibody|TDO antibody
Anti-DLX3 antibody (ab64953)
Close sc-134317|sc-514094|sc-18143|sc-98522|

Recommended applications: ELISA, IHC

Recommended dilution: Recommended dilution:IHC:1:20-1:200

Recommended protocols: check protocols

Name

Anti-DLX3 Antibody

Catalogue No.

CSB-PA006954ESR2HU

Reactivity

Human

Immunogen

Recombinant human Homeobox protein DLX-3 protein (1-120AA)

Host

Rabbit

Applications

ELISA, IHC

Recommended dilution

Recommended dilution:IHC:1:20-1:200

Clonality

Polyclonal

Conjugation

unconjugated

Isotype

IgG

Molecular weight

31 kDa

Purification

Antigen Affinity Purified

Storage

Shipped at 4 Celcius Degree. Upon delivery aliquot and store at -20 Celcius Degree or -80 Celcius Degree. Avoid repeated freeze.

Database links

Entrez Gene:1747( Human), Entrez Gene:13393( Mouse), Omim:600525( Human), SwissProt:O60479( Human), SwissProt:Q64205( Mouse), Unigene:134194( Human), Unigene:5194( Mouse)

Protein function

Likely to play a regulatory role in the development of the ventral forebrain. May play a role in craniofacial patterning and morphogenesis.

Involvement in disease

Trichodentoosseous syndrome (TDO) [MIM:190320]: An autosomal dominant disease characterized by curly kinky hair at birth, enamel hypoplasia, taurodontism, thickening of cortical bones and variable expression of craniofacial morphology. . Note=The disease is caused by mutations affecting the gene represented in this entry.; Amelogenesis imperfecta 4 (AI4) [MIM:104510]: An autosomal dominant defect of enamel formation associated with enlarged pulp chambers. Enamel is thin, teeth are small and widely spaced. . Note=The disease is caused by mutations affecting the gene represented in this entry.

Protein sequence and domain

Belongs to the distal-less homeobox family.

Protein cellular localization

Nucleus .

Note

AntibodyPlus provides antibody trial sample for your own antibody validation and collects antibody reviews.

Supplier

CUSABIO BIOTECH CO.

Product type

Primary antibody

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