MSX1 Antikörper (AA 111-138)

Produktnummer ABIN1537757

Produktdetails anti-MSX1 Antikörper

Target: MSX1 (Msh Homeobox 1 (MSX1))

Bindungsspezifität: AA 111-138

Reaktivität: Human, Maus

Wirt: Kaninchen

Klonalität: Polyklonal

Konjugat: Dieser MSX1 Antikörper ist unkonjugiert

Applikation: Western Blotting (WB), Immunofluorescence (IF)

Homologie: B

Aufreinigung: This antibody is purified through a protein A column, followed by peptide affinity purification.

Immunogen: This MSX1 antibody is generated from rabbits immunized with a KLH conjugated synthetic peptide between 111-138 amino acids from the Central region of human MSX1.

Klon: RB30384

Isotyp: Ig Fraction

Anwendungsinformationen

Applikationshinweise: IF: 1:10~50. IF: 1:200. WB: 1:1000. WB: 1:2000. WB: 1:1000

Beschränkungen: Nur für Forschungszwecke einsetzbar

Handhabung

Format: Liquid

Buffer: Purified polyclonal antibody supplied in PBS with 0.09 % (W/V) 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: 4 °C,-20 °C

Informationen zur Lagerung: MSX1 Antibody (Center) can be refrigerated at 2-8 °C for up to 6 months. For long term storage, keep at -20 °C.

Haltbarkeit: 6 months

Details zu MSX1

Target: MSX1 (Msh Homeobox 1 (MSX1))

Andere Bezeichnung: MSX1 (MSX1 Produkte)

Synonyme: ECTD3 antikoerper, HOX7 antikoerper, HYD1 antikoerper, STHAG1 antikoerper, AA675338 antikoerper, AI324650 antikoerper, Hox-7 antikoerper, Hox7 antikoerper, Hox7.1 antikoerper, msh antikoerper, CHOX-7 antikoerper, GHOX-7 antikoerper, HOX-7 antikoerper, msh homeobox 1 antikoerper, MSX1 antikoerper, Msx1 antikoerper

Hintergrund: This gene encodes a member of the muscle segment homeobox gene family. The encoded protein functions as a transcriptional repressor during embryogenesis through interactions with components of the core transcription complex and other homeoproteins. It may also have roles in limb-pattern formation, craniofacial development, particularly odontogenesis, and tumor growth inhibition. Mutations in this gene, which was once known as homeobox 7, have been associated with nonsyndromic cleft lip with or without cleft palate 5, Witkop syndrome, Wolf-Hirschom syndrome, and autosomoal dominant hypodontia.

Molekulargewicht: 31496

Gen-ID: 4487

NCBI Accession: NP_002439

UniProt: P28360

Pathways: Regulation of Muscle Cell Differentiation, Positive Regulation of Response to DNA Damage Stimulus