Anti-PAX3 antibody (ab50193)
- Datasheet
- References
- Protocols
Overview
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Product nameAnti-PAX3 antibody
See all PAX3 primary antibodies -
DescriptionRabbit polyclonal to PAX3
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Host speciesRabbit
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SpecificityReactive with PAX3. A customer Abreview from January 2011 demonstrates the development-specific expression.
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Tested applicationsSuitable for: WB, ELISAmore details
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Species reactivityReacts with: Mouse, Human
Predicted to work with: Rat, Rabbit, Goat, Horse, Chicken, Guinea pig, Cow, Cat, Dog -
Immunogen
Synthetic peptide within Human PAX3 aa 164-213 (internal sequence). The exact sequence is proprietary.
Sequence:KGEEEEADLERKEAEESEKKAKHSIDGILSERASAPQSDEGSDIDSEPDL
Database link: P23760 -
Positive control
- Fetal liver lysate
Properties
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FormLiquid
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Storage instructionsShipped at 4°C. Upon delivery aliquot and store at -20°C. Avoid freeze / thaw cycles.
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Storage bufferPreservative: 0.09% Sodium azide
Constituents: 2% Sucrose, PBS -
Concentration information loading...
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PurityProtein A purified
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ClonalityPolyclonal
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IsotypeIgG
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Research areas
Associated products
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Compatible Secondaries
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Isotype control
Applications
Our Abpromise guarantee covers the use of ab50193 in the following tested applications.
The application notes include recommended starting dilutions; optimal dilutions/concentrations should be determined by the end user.
Application | Abreviews | Notes |
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WB | Use a concentration of 2.5 µg/ml. Detects a band of approximately 42 kDa (predicted molecular weight: 53 kDa). Good results were obtained when blocked with 5% non-fat dry milk in 0.05% PBS-T. | |
ELISA | 1/312500. |
Target
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FunctionProbable transcription factor associated with development of alveolar rhabdomyosarcoma.
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Involvement in diseaseDefects in PAX3 are the cause of Waardenburg syndrome type 1 (WS1) [MIM:193500]. WS1 is an autosomal dominant disorder characterized by wide bridge of nose owing to lateral displacement of the inner canthus of each eye (dystopia canthorum), pigmentary disturbances such as frontal white blaze of hair, heterochromia of irides, white eyelashes, leukoderma and sensorineural deafness. The syndrome shows variable clinical expression and some affected individuals do not manifest hearing impairment.
Defects in PAX3 are the cause of Waardenburg syndrome type 3 (WS3) [MIM:148820]; also known as Klein-Waardenburg syndrome or Waardenburg syndrome with upper limb anomalies or white forelock with malformations. WS3 is a very rare autosomal dominant disorder, which shares many of the characteristics of WS1. Patients additionally present with musculoskeletal abnormalities.
Defects in PAX3 are the cause of craniofacial-deafness-hand syndrome (CDHS) [MIM:122880]. CDHS is thought to be an autosomal dominant disease which comprises absence or hypoplasia of the nasal bones, hypoplastic maxilla, small and short nose with thin nares, limited movement of the wrist, short palpebral fissures, ulnar deviation of the fingers, hypertelorism and profound sensory-neural deafness.
Defects in PAX3 are a cause of rhabdomyosarcoma type 2 (RMS2) [MIM:268220]. It is a form of rhabdomyosarcoma, a highly malignant tumor of striated muscle derived from primitive mesenchimal cells and exhibiting differentiation along rhabdomyoblastic lines. Rhabdomyosarcoma is one of the most frequently occurring soft tissue sarcomas and the most common in children. It occurs in four forms: alveolar, pleomorphic, embryonal and botryoidal rhabdomyosarcomas. Note=A chromosomal aberration involving PAX3 is found in rhabdomyosarcoma. Translocation (2;13)(q35;q14) with FOXO1. The resulting protein is a transcriptional activator.
Note=A chromosomal aberration involving PAX3 is a cause of rhabdomyosarcoma. Translocation t(2;2)(q35;p23) with NCOA1 generates the NCOA1-PAX3 oncogene consisting of the N-terminus part of PAX3 and the C-terminus part of NCOA1. The fusion protein acts as a transcriptional activator. Rhabdomyosarcoma is the most common soft tissue carcinoma in childhood, representing 5-8% of all malignancies in children. -
Sequence similaritiesBelongs to the paired homeobox family.
Contains 1 homeobox DNA-binding domain.
Contains 1 paired domain. -
Cellular localizationNucleus.
- Information by UniProt
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Database links
- Entrez Gene: 5077 Human
- Entrez Gene: 18505 Mouse
- Entrez Gene: 114502 Rat
- Omim: 606597 Human
- SwissProt: P23760 Human
- SwissProt: P24610 Mouse
- Unigene: 42146 Human
- Unigene: 1371 Mouse
see all -
Alternative names
- CDHS antibody
- HUP 2 antibody
- HUP2 antibody
see all
Images
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Anti-PAX3 antibody (ab50193) at 2.5 µg/ml + Fetal liver lysate at 10 µg
Secondary
HRP conjugated anti-Rabbit IgG at 1/50000 dilution
Predicted band size: 53 kDa
Observed band size: 42 kDa why is the actual band size different from the predicted? -
All lanes : Anti-PAX3 antibody (ab50193) at 1/1000 dilution
Lane 1 : Whole tissue lysate prepared from mouse cerebellum (post natal 4 days)
Lane 2 : Whole tissue lysate prepared from mouse cerebellum (adult)
Lane 3 : Whole tissue lysate prepared from mouse kidney (adult)
Lysates/proteins at 20 µg per lane.
Secondary
All lanes : HRP conjugated mouse monoclonal at 1/10000 dilution
Predicted band size: 53 kDa
Blocking step was performed using 5% milk for 1 hour at 20°C.
Protocols
Datasheets and documents
References
ab50193 has not yet been referenced specifically in any publications.