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Rabbit Anti-HOXA1 Antibody (CSB-PA010647DSR2HU)
Supplier: CUSABIO BIOTECH CO.
Homeobox protein Hox-1F Antibody,HOXA1 Antibody,HOX1F AntibodyMore alternative names for the antibody
BSAS antibody|Homeo box A1 antibody|Homeobox 1F antibody|Homeobox A1 antibody|Homeobox protein Hox A1 antibody|Homeobox protein Hox-1F antibody|Homeobox protein Hox-A1 antibody|Hox 1.6 like protein antibody|Hox 1F antibody|HOX A1 antibody|HOX A1 homeodomain protein antibody|HOX1 antibody|HOX1F antibody|hoxa1 antibody|hoxb1b antibody|HXA1_HUMAN antibody|Lab like protein antibody|MGC45232 antibody
Anti-HOXA1 antibody (ab208781)
Anti-HOXA1 antibody (ab208781)
Recommended applications: ELISA, IHC
Recommended dilution: Recommended dilution:IHC:1:20-1:200
Recommended protocols: check protocols
|Catalogue No.|| |
Recombinant human Homeobox protein Hox-A1 protein (75-205AA)
|Recommended dilution|| |
|Molecular weight|| |
Antigen Affinity Purified
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:3198( Human), Entrez Gene:15394( Mouse), Entrez Gene:30374( Zebrafish), Omim:142955( Human), SwissProt:P49639( Human), SwissProt:P09022( Mouse), SwissProt:O08656( Rat), SwissProt:Q90423( Zebrafish), SwissProt:Q98SI1( Zebrafish), Unigene:67397( Human), Unigene:197( Mouse), Unigene:228589( Rat), Unigene:9780( Rat)
|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. Seems to act in the maintenance and/or generation of hindbrain segments.
|Involvement in disease|| |
Athabaskan brainstem dysgenesis syndrome (ABDS) [MIM:601536]: Characterized by horizontal gaze palsy, sensorineural deafness, central hypoventilation, and developmental delay. Some patients had swallowing dysfunction, vocal cord paralysis, facial paresis, seizures, and cardiac outflow tract anomalies. . Note=The disease is caused by mutations affecting the gene represented in this entry.; Bosley-Salih-Alorainy syndrome (BSAS) [MIM:601536]: A disease characterized by horizontal gaze abnormalities, deafness, facial weakness, vascular malformations of the internal carotid arteries and cardiac outflow trac. Some patients manifest mental retardation and autism spectrum disorder. Affected individuals do not suffer from central hypoventilation. 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|| |
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|Product type|| |
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