SHOX2 Antikörper
-
- Target Alle SHOX2 Antikörper anzeigen
- SHOX2 (Short Stature Homeobox 2 (SHOX2))
-
Reaktivität
- Human, Ratte, Maus
-
Wirt
- Kaninchen
-
Klonalität
- Polyklonal
-
Konjugat
- Dieser SHOX2 Antikörper ist unkonjugiert
-
Applikation
- Western Blotting (WB)
- Produktmerkmale
- Polyclonal Antibody
- Aufreinigung
- Affinity purification
- Immunogen
- Recombinant fusion protein of human SHOX2 (NP_003021.3).
- Isotyp
- IgG
- Top Product
- Discover our top product SHOX2 Primärantikörper
-
-
- Applikationshinweise
- WB 1:500-1:2000
- Beschränkungen
- Nur für Forschungszwecke einsetzbar
-
- Format
- Liquid
- Konzentration
- 1 mg/mL
- Buffer
- PBS with 0.02 % sodium azide, 50 % glycerol, pH 7.3
- Konservierungsmittel
- Sodium azide
- Vorsichtsmaßnahmen
- This product contains Sodium azide: a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.
- Lagerung
- -20 °C
- Informationen zur Lagerung
- Store at -20°C. Avoid freeze / thaw cycles.
-
- Target
- SHOX2 (Short Stature Homeobox 2 (SHOX2))
- Andere Bezeichnung
- SHOX2 (SHOX2 Produkte)
- Synonyme
- SHOX2 antikoerper, og12 antikoerper, shot antikoerper, og12x antikoerper, ogi2x antikoerper, OG12 antikoerper, OG12X antikoerper, SHOT antikoerper, 6330543G17Rik antikoerper, Og12x antikoerper, Prx3 antikoerper, zgc:65884 antikoerper, zgc:77344 antikoerper, short stature homeobox 2 antikoerper, SHOX2 antikoerper, shox2 antikoerper, Shox2 antikoerper
- Hintergrund
- This gene is a member of the homeobox family of genes that encode proteins containing a 60-amino acid residue motif that represents a DNA binding domain. Homeobox genes have been characterized extensively as transcriptional regulators involved in pattern formation in both invertebrate and vertebrate species. Several human genetic disorders are caused by aberrations in human homeobox genes. This locus represents a pseudoautosomal homeobox gene that is thought to be responsible for idiopathic short stature, and it is implicated in the short stature phenotype of Turner syndrome patients. This gene is considered to be a candidate gene for Cornelia de Lange syndrome. Alternative splicing results in multiple transcript variants.
- Molekulargewicht
-
Observed_MW: 30 kDa
Calculated_MW: 33 kDa/34 kDa/37 kDa
- Gen-ID
- 6474
- UniProt
- O60902
- Pathways
- Regulation of Muscle Cell Differentiation, Skeletal Muscle Fiber Development
-