Anti-HOXB1 Antibody

$99.00$319.00

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

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Rabbit Anti-HOXB1 Antibody (CSB-PA010660ESR1HU)

Supplier: CUSABIO BIOTECH CO.

Alternative names:

Homeobox protein Hox-2I Antibody,HOXB1 Antibody,HOX2I Antibody

More alternative names for the antibody
HCFP3 antibody|Homeo box 2I antibody|Homeo box B1 antibody|Homeobox 2I antibody|Homeobox B1 antibody|Homeobox protein Hox B1 antibody|Homeobox protein Hox-2I antibody|Homeobox protein Hox-B1 antibody|Homeobox protein HoxB1 antibody|Homeobox2I antibody|HomeoboxB1 antibody|HOX 2 antibody|Hox 2.9 antibody|HOX 2I antibody|HOX B1 antibody|HOX2 antibody|Hox2.9 antibody|HOX2I antibody|HOXB 1 antibody|HOXB1 antibody|HOXB1 protein antibody|HXB1_HUMAN antibody|MGC116843 antibody|MGC116844 antibody|MGC116845 antibody
Anti-HOXB1 antibody (ab168279)
Close sc-17161|sc-17162|

Recommended applications: ELISA, WB

Recommended dilution: Recommended dilution:WB:1:200-1000

Recommended protocols: check protocols

Name

Anti-HOXB1 Antibody

Catalogue No.

CSB-PA010660ESR1HU

Reactivity

Human, Mouse

Immunogen

Recombinant human Homeobox protein Hox-B1 protein (35-180AA)

Host

Rabbit

Applications

ELISA, WB

Recommended dilution

Recommended dilution:WB:1:200-1000

Clonality

Polyclonal

Conjugation

unconjugated

Isotype

IgG

Molecular weight

32 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:3211( Human), Entrez Gene:100434039( Orangutan), Omim:142968( Human), SwissProt:A2T6Z0( Chimpanzee), SwissProt:P14653( Human), SwissProt:A2T6H5( Macaque Monkey), SwissProt:A2T7J2( Orangutan), Unigene:99992( Human)

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. Acts on the anterior body structures.

Involvement in disease

Facial paresis, hereditary congenital, 3 (HCFP3) [MIM:614744]: A form of facial paresis, a disease characterized by isolated dysfunction of the facial nerve (CN VII). HCFP3 patients are affected by bilateral facial palsy, facial muscle weakness of muscles innervated by CN VII, hearing loss, and strabismus. . Note=The disease is caused by mutations affecting the gene represented in this entry.

Protein sequence and domain

Belongs to the Antp homeobox family. Labial subfamily.

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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