SHOX2 Antikörper (AA 96-355)

Produktnummer ABIN6147751

Dieses Kaninchen Polyklonal-Antikörper erkennt spezifisch SHOX2 in WB. Er zeigt eine Reaktivität gegenüber Human.

Kurzübersicht für SHOX2 Antikörper (AA 96-355) (ABIN6147751)

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

Reaktivität: Human

Wirt: Kaninchen

Klonalität: Polyklonal

Konjugat: Dieser SHOX2 Antikörper ist unkonjugiert

Applikation: Western Blotting (WB)

Produktdetails anti-SHOX2 Antikörper

Bindungsspezifität: AA 96-355

Sequenz: ELDMGAAERS REPGSPRLTE GRRKPTKAEV QATLLLPGEA FRFLVSPELK DRKEDAKGME DEGQTKIKQR RSRTNFTLEQ LNELERLFDE THYPDAFMRE ELSQRLGLSE ARVQVWFQNR RAKCRKQENQ LHKGVLIGAA SQFEACRVAP YVNVGALRMP FQQDSHCNVT PLSFQVQAQL QLDSAVAHAH HHLHPHLAAH APYMMFPAPP FGLPLATLAA DSASAASVVA AAAAAKTTSK NSSIADLRLK AKKHAAALGL

Kreuzreaktivität: Human, Maus, Ratte

Produktmerkmale: Polyclonal Antibodies

Immunogen: Recombinant fusion protein containing a sequence corresponding to amino acids 96-355 of human SHOX2 (NP_003021.3).

Isotyp: IgG

Anwendungsinformationen

Applikationshinweise: WB,1:500 - 1:2000

Kommentare:

HIGH QUALITY

Beschränkungen: Nur für Forschungszwecke einsetzbar

Handhabung

Format: Liquid

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.

Details zu SHOX2

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

Andere Bezeichnung: SHOX2

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.,SHOX2,OG12,OG12X,SHOT,Epigenetics & Nuclear Signaling,Transcription Factors,SHOX2

Molekulargewicht: 33 kDa/34 kDa/37 kDa

Gen-ID: 6474

UniProt: O60902

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