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Hox-A1 Polyclonal Antibody

Polyclonal antibody

Specification

BYab-15758

  • 50UL $180 100UL $255
  • Delivery: In Stock

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Host
Reactiveness
Use
Molecular weight (DA)
37kD
Immunogen
The antiserum was produced against synthesized peptide derived from human HOXA1. AA range:171-220
Specificity
Hox-A1 Polyclonal Antibody detects endogenous levels of Hox-A1 protein.
Source
Formulation
Liquid in PBS containing 50% glycerol, 0.5% BSA and 0.02% sodium azide.
Dilution rate
WB: 1/500 - 1/2000. IHC: 1/100 - 1/300. ELISA: 1/20000.. IF 1:50-200
Purification process (Immunogen)
The antibody was affinity-purified from rabbit antiserum by affinity-chromatography using epitope-specific immunogen.
Concentration
1 mg/ml
Background
In vertebrates, the genes encoding the class of transcription factors called homeobox genes are found in clusters named A, B, C, and D on four separate chromosomes. Expression of these proteins is spatially and temporally regulated during embryonic development. This gene is part of the A cluster on chromosome 7 and encodes a DNA-binding transcription factor which may regulate gene expression, morphogenesis, and differentiation. The encoded protein may be involved in the placement of hindbrain segments in the proper location along the anterior-posterior axis during development. Two transcript variants encoding two different isoforms have been found for this gene, with only one of the isoforms containing the homeodomain region. [provided by RefSeq, Jul 2008],
Function
disease:Defects in HOXA1 are the cause of Athabaskan brainstem dysgenesis syndrome (ABSD) [MIM:601536]; also known as Narvajo brainstem syndrome. This syndrome is 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.,disease:Defects in HOXA1 are the cause of Bosley-Salih-Alorainy syndrome (BSAS) [MIM:601536]. Affected individuals show 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. In contrast to individuals with ABSD, central hypoventilation is not observed in individuals with BSAS.,function:Sequence-specific transcription factor which is par
Gene Name
HOXA1
Protein name
Homeobox protein Hox-A1
Abbreviation
Hox-A1
Other name
HOXA1; HOX1F; Homeobox protein Hox-A1; Homeobox protein Hox-1F
Fields
>>Signaling pathways regulating pluripotency of stem cells
Human gene ID
3198
Human protein sequence Database
P49639
Mouse gene ID
Mouse protein sequence database
P09022
Rat gene ID
25607
Rat protein sequence database
O08656
Cellular localization
Nucleus .
Tissue expression
Ovary,Skin,
Storage
-20°C/1 year

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Hox-A1 Polyclonal Antibody

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