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ATRX Polyclonal Antibody

ArtNr E-AB-19609-120
Hersteller Elabscience
Menge 120 uL
Quantity options 120 uL 20 uL 200 uL 60 uL
Kategorie
Typ Antibody Polyclonal
Applikationen IHC
Specific against Human (Homo sapiens), Mouse (Murine, Mus musculus)
Host Rabbit
Isotype IgG
Konjugat/Tag Unconjugated
ECLASS 10.1 32160702
ECLASS 11.0 32160702
UNSPSC 12352203
Alias Alpha thalassemia/mental retardation syndrome X linked homolog, ATP dependent helicase ATRX, ATP-dependent helicase ATRX, ATR2, Atrx, ATRX, DNA dependent ATPase and helicase, Helicase 2, X linked, MGC2094, MRXHF1, RAD54, RAD54L, SFM1, SHS, Transcriptional regulator ATRX, X linked helicase II, X linked nuclear protein, X-linked helicase II, X-linked nuclear protein, XH2, XNP, Znf HX, Znf-HX
Similar products RAD54L, ATRX, Atrx, ATR2, XNP, MGC2094, MRXHF1, RAD54, SFM1, SHS, XH2, DNA dependent ATPase and helicase, X-linked nuclear protein, X linked, Transcriptional regulator ATRX, ATP-dependent helicase ATRX, Helicase 2, X-linked helicase II, Znf-HX, Alpha thalassemia/mental retardation syndrome X linked homolog, ATP dependent helicase ATRX, X linked helicase II, X linked nuclear protein, Znf HX
Versandbedingung Gekühlt
Gefahren-Info Comply with cargo safety certificate
Lieferbar
Manufacturer - Category
Primary Antibodies
Manufacturer - Targets
ATRX
Shipping Temperature
The product is shipped with ice pack, upon receipt, store it immediately at the temperature recommended.
Storage Conditions
Store at -20°C Valid for 12 months. Avoid freeze / thaw cycles.
Manufacturer - Research Areas
Epigenetics and Nuclear Signaling
Background
The protein encoded by this gene contains an ATPase/helicase domain, and thus it belongs to the SWI/SNF family of chromatin remodeling proteins. This protein is found to undergo cell cycle-dependent phosphorylation, which regulates its nuclear matrix and chromatin association, and suggests its involvement in the gene regulation at interphase and chromosomal segregation in mitosis. Mutations in this gene are associated with an X-linked mental retardation (XLMR) syndrome most often accompanied by alpha-thalassemia (ATRX) syndrome. These mutations have been shown to cause diverse changes in the pattern of DNA methylation, which may provide a link between chromatin remodeling, DNA methylation, and gene expression in developmental processes. Multiple alternatively spliced transcript variants encoding distinct isoforms have been reported.
Concentration
0.7 mg/mL
Buffer
PBS with 0.05% NaN3 and 40% Glycerol, pH7.4
Purification Method
Antigen affinity purification
Recommended Dilution
IHC 1:30-1:150
Abbreviation
ATRX
Clonality
Polyclonal
Immunogen
Synthetic peptide of human ATRX
Category ID III
Polyclonal Antibodies

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Alle Produkte sind nur für Forschungszwecke bestimmt. Nicht für den menschlichen, tierärztlichen oder therapeutischen Gebrauch.

Menge: 120 uL
Lieferbar: In stock
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