SHOX2 Antikörper (AA 37-87)

Produktnummer ABIN8124660

Der Kaninchen Polyklonal anti-SHOX2 Antikörper wird verwendet zum Nachweis von SHOX2 in Proben von Human, Ratte und Maus. Er wurde validiert für WB, IHC und FACS.

Kurzübersicht für SHOX2 Antikörper (AA 37-87) (ABIN8124660)

Target: SHOX2 (Short Stature Homeobox 2 (SHOX2))

Reaktivität: Human, Ratte, Maus

Wirt: Kaninchen

Klonalität: Polyklonal

Konjugat: Dieser SHOX2 Antikörper ist unkonjugiert

Applikation: Western Blotting (WB), Immunohistochemistry (IHC), Flow Cytometry (FACS)

Produktdetails anti-SHOX2 Antikörper

Bindungsspezifität: AA 37-87

Verwendungszweck: SHOX2 Antibody

Spezifität: This antibody detects endogenous levels of SHOX2 at Human/Mouse/Rat

Aufreinigung: The antibody was affinity-purified from rabbit antiserum by affinity-chromatography using epitope-specific immunogen.

Immunogen: Synthesized peptide derived from human SHOX2 AA range: 37-87

Isotyp: IgG

Anwendungsinformationen

Applikationshinweise: WB 1:500-2000,IHC 1:50-300,FCM 1:100-200

Beschränkungen: Nur für Forschungszwecke einsetzbar

Handhabung

Format: Liquid

Buffer: Liquid in PBS containing 50 % glycerol, 0.5 % BSA and 0.02 % sodium azide.

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/1 year

Haltbarkeit: 12 months

Details zu SHOX2

Target: SHOX2 (Short Stature Homeobox 2 (SHOX2))

Andere Bezeichnung: SHOX2

Hintergrund:

Background: 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. [provided by RefSeq, Jul 2009],

Gene Name: SHOX2 OG12X SHOT

Protein Name: SHOX2

Gen-ID: 6474

UniProt: O60902

Pathways: Regulation of Muscle Cell Differentiation, Skeletal Muscle Fiber Development