Anti-HOXD10 Antibody

$99.00$319.00

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

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Rabbit Anti-HOXD10 Antibody (CSB-PA010682ESR2HU)

Supplier: CUSABIO BIOTECH CO.

Alternative names:

Homeobox protein Hox-D10 Antibody,Homeobox protein Hox-4D Antibody,Homeobox protein Hox-4E Antibody,HOXD10 Antibody,HOX4D Antibody,HOX4E Antibody

More alternative names for the antibody
AI385591 antibody|AI874987 antibody|Homeo box 4D antibody|Homeo box D10 antibody|Homeobox D10 antibody|Homeobox protein Hox-4D antibody|Homeobox protein Hox-4E antibody|Homeobox protein Hox-D10 antibody|Hox 4.4 antibody|Hox 4.5 antibody|Hox 4D antibody|Hox 4E antibody|Hox 5.3 antibody|HOX4D antibody|HOX4E antibody|HOXD10 antibody|HXD10 antibody|HXD10_HUMAN antibody|OTTMUSP00000017845 antibody|RP23-313J15.9 antibody
Anti-HOXD10 antibody [EPR9374] (ab138508)
Close sc-166233|sc-166235|sc-66926|sc-33006|

Recommended applications: ELISA, WB, IHC

Recommended dilution: User optimized

Recommended protocols: check protocols

Name

Anti-HOXD10 Antibody

Catalogue No.

CSB-PA010682ESR2HU

Reactivity

Human, Mouse

Immunogen

Recombinant human Homeobox protein Hox-D10 protein (1-240AA)

Host

Rabbit

Applications

ELISA, WB, IHC

Recommended dilution

User optimized

Clonality

Polyclonal

Conjugation

unconjugated

Isotype

IgG

Molecular weight

38 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:3236( Human), Entrez Gene:15430( Mouse), Omim:142984( Human), SwissProt:P28358( Human), SwissProt:P28359( Mouse), Unigene:123070( Human), Unigene:24420( Mouse)

Protein function

Sequence-specific transcription factor which is part of a developmental regulatory system that provides cells with specific positional identities on the anterior-posterior axis.

Protein tissue specificity

Strongly expressed in the adult male and female urogenital tracts.

Involvement in disease

Vertical talus, congenital (CVT) [MIM:192950]: A rare malformation characterized by vertical orientation of the talus with a rigid dorsal dislocation of the navicular, equinus deformity of the calcaneus, abduction deformity of the forefoot, and contracture of the soft tissues of the hind- and mid-foot. This condition is usually associated with multiple other congenital deformities and only rarely is an isolated deformity with familial occurrence. . Note=The disease is caused by mutations affecting the gene represented in this entry.

Protein sequence and domain

Belongs to the Abd-B 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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