anti-Short Stature Homeobox (SHOX) Antikörper

SHOX belongs to the paired homeobox family and is located in the pseudoautosomal region 1 (PAR1) of X and Y chromosomes. Zusätzlich bieten wir Ihnen SHOX Proteine (2) und viele weitere Produktgruppen zu diesem Protein an.

Alle Antikörper anzeigen Gen GeneID UniProt
SHOX 6473 O15266
SHOX    
SHOX    
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Top anti-SHOX Antikörper auf antikoerper-online.de

Showing 10 out of 29 products:

Katalog Nr. Reaktivität Wirt Konjugat Applikation Bilder Menge Anbieter Lieferzeit Preis Details
Rind (Kuh) Kaninchen Unkonjugiert WB WB Suggested Anti-SHOX Antibody Titration: 0.2-1 ug/ml ELISA Titer: 1:312500 Positive Control: Human brain 100 μL Anmelden zum Anzeigen 6 bis 8 Tage
358,51 €
Details
Huhn Kaninchen Unkonjugiert WB 50 μg Anmelden zum Anzeigen 11 bis 14 Tage
653,02 €
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Huhn Kaninchen Unkonjugiert WB Western blot analysis of SHOX expression in HEK293T (A), Raw264.7 (B), SP2/0 (C) whole cell lysates. 200 μL Anmelden zum Anzeigen 11 bis 13 Tage
464,29 €
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Human Kaninchen Unkonjugiert ELISA, WB 50 μg Anmelden zum Anzeigen 6 bis 8 Tage
459,65 €
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Human Kaninchen Unkonjugiert ICC, IF Immunocytochemistry/Immunofluorescence: SHOX Antibody  - Staining of human cell line BJ shows localization to nucleoplasm & vesicles. 100 μL Anmelden zum Anzeigen 5 bis 8 Tage
335,00 €
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Human Kaninchen Unkonjugiert ELISA, WB   200 μL Anmelden zum Anzeigen 11 bis 14 Tage
941,11 €
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Human Kaninchen HRP ELISA, WB   200 μL Anmelden zum Anzeigen 11 bis 14 Tage
1.203,02 €
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Human Kaninchen Alkaline Phosphatase (AP) ELISA, WB   200 μL Anmelden zum Anzeigen 11 bis 14 Tage
1.203,02 €
Details
Human Kaninchen APC ELISA, WB   200 μL Anmelden zum Anzeigen 11 bis 14 Tage
1.203,02 €
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Human Kaninchen FITC ELISA, WB   200 μL Anmelden zum Anzeigen 11 bis 14 Tage
1.203,02 €
Details

SHOX Antikörper nach Reaktivität, Anwendung, Klonalität and Konjugat

Attribute Applikationen Wirt Klonalität Konjugat
Human ,
,

, , , , ,
Mouse (Murine)


Dog (Canine)


Weitere Antikörper gegen SHOX Interaktionspartner

Zebrafish Short Stature Homeobox (SHOX) Interaktionspartner

  1. demonstrate evolutionarily conserved Shox plays roles in early embryonic growth and in later bone formation.

  2. The expression pattern of the shox gene across the whole embryo and characterise the enhancer domains of different conserved non-coding elements associated with this gene, is reported.

Human Short Stature Homeobox (SHOX) Interaktionspartner

  1. A concomitant duplication of SHOX enhancers may be required to trigger a NDD in females.

  2. Together, these findings describe CYP26C1 as the first genetic modifier for SHOX deficiency.

  3. SHOX duplications encompassing CNE-9 enhancer are highly penetrant alleles for Leri-Weill dyschondrosteosis.

  4. Evaluation of the data and that in the literature reveals that although partial deletions and duplications only account for a small fraction of SHOX alterations, intron 3 appears to be a breakpoint hotspot, with alterations arising by non-allelic homologous recombination, non-homologous end joining or other complex mechanisms.

  5. Genotype-Phenotype Relationship in Patients and Relatives with SHOX Region Anomalies in the French Population.

  6. This study shows that expressing human SHOX in Shox2SHOX KI/KI (zeige PSME3 Antikörper) mice leads to congenital osteoarthritislike disease of the temporomandibular joint in postnatal mice. This provides a novel in vivo model for studying the molecular and cellular mechanisms of temporomandibular joint osteoarthritis.

  7. we detected an SHOX gene deletion in 1 of 38 children with idiopathic short stature

  8. The 15523-bp SHOX intragenic deletion, encompassing exons 3-6, was initially detected by array-CGH, followed by MLPA analysis. Sequencing of the breakpoints indicated an Alu recombination-mediated deletion (ARMD) as the potential causative mechanism.

  9. this study highlights the clinical importance and genetic heterogeneity of the SHOX-flanking CNVs, and indicates a limited clinical significance of point mutations in the CNEs.

  10. SHOX haploinsufficiency is associated with 45,X disorder of sexual differentiation.

SHOX Antigen-Profil

Protein Überblick

This gene belongs to the paired homeobox family and is located in the pseudoautosomal region 1 (PAR1) of X and Y chromosomes. Defects in this gene are associated with idiopathic growth retardation and in the short stature phenotype of Turner syndrome patients. This gene is highly conserved across species from mammals to fish to flies. Alternatively spliced transcript variants encoding different isoforms have been noted for this gene.

Genbezeichner und Symbole assoziert mit SHOX

  • short stature homeobox (shox) Antikörper
  • short stature homeobox (SHOX) Antikörper
  • GCFX Antikörper
  • PHOG Antikörper
  • SHOXY Antikörper
  • si:ch211-134k13.1 Antikörper
  • SS Antikörper
  • zgc:123182 Antikörper

Bezeichner auf Proteinebene für SHOX

short stature homeobox protein , growth control factor, X-linked , pseudoautosomal homeobox-containing osteogenic protein

GENE ID SPEZIES
664748 Danio rerio
418669 Gallus gallus
491706 Canis lupus familiaris
615159 Bos taurus
6473 Homo sapiens
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