MAGE-Like 2 Antikörper
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- Target Alle MAGE-Like 2 (MAGEL2) Antikörper anzeigen
- MAGE-Like 2 (MAGEL2)
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Reaktivität
- Human, Maus, Ratte
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Wirt
- Kaninchen
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Klonalität
- Polyklonal
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Konjugat
- Dieser MAGE-Like 2 Antikörper ist unkonjugiert
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Applikation
- ELISA, Western Blotting (WB)
- Aufreinigung
- Antigen affinity purification
- Immunogen
- Synthetic peptide of human MAGEL2
- Isotyp
- IgG
- Top Product
- Discover our top product MAGEL2 Primärantikörper
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anti-MAGE-Like 2 (MAGEL2) (AA 499-529), (C-Term) antibody
MAGEL2 Reaktivität: Human WB, IHC (p) Wirt: Kaninchen Polyclonal RB2131 unconjugated
anti-MAGE-Like 2 (MAGEL2) antibodyMAGEL2 Reaktivität: Human ELISA, WB Wirt: Kaninchen Polyclonal unconjugated
anti-MAGE-Like 2 (MAGEL2) (N-Term) antibodyMAGEL2 Reaktivität: Human, Rind (Kuh), Hund, Schwein, Kaninchen, Affe WB Wirt: Kaninchen Polyclonal unconjugated
anti-MAGE-Like 2 (MAGEL2) (N-Term) antibodyMAGEL2 Reaktivität: Human, Rind (Kuh), Hund, Schwein, Kaninchen WB Wirt: Kaninchen Polyclonal unconjugated
anti-MAGE-Like 2 (MAGEL2) (N-Term) antibodyMAGEL2 Reaktivität: Human WB, IHC (p), EIA Wirt: Kaninchen Polyclonal unconjugated
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- Applikationshinweise
- Optimal working dilution should be determined by the investigator.
- Beschränkungen
- Nur für Forschungszwecke einsetzbar
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- Format
- Liquid
- Handhabung
- Avoid freeze / thaw cycles.
- Lagerung
- -20 °C/-80 °C
- Informationen zur Lagerung
- Store at -20°C (regular) and -80°C (long term).
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- Target
- MAGE-Like 2 (MAGEL2)
- Andere Bezeichnung
- MAGEL2 (MAGEL2 Produkte)
- Synonyme
- NDNL1 antikoerper, nM15 antikoerper, MAGEL2 antikoerper, Mage-l2 antikoerper, ns7 antikoerper, MAGE family member L2 antikoerper, melanoma antigen, family L, 2 antikoerper, MAGEL2 antikoerper, Magel2 antikoerper
- Hintergrund
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Prader-Willi syndrome (PWS) is caused by the loss of expression of imprinted genes in chromosome 15q11-q13 region. Affected individuals exhibit neonatal hypotonia, developmental delay, and childhood-onset obesity. Necdin (NDN), a gene involved in the terminal differentiation of neurons, localizes to this region of the genome and has been implicated as one of the genes responsible for the etiology of PWS. This gene is structurally similar to NDN, is also localized to the PWS chromosomal region, and is paternally imprinted, suggesting a possible role for it in PWS.
Synonyms: PWLS, nM15, NDNL1 - Molekulargewicht
- Calculated MW: 59 kDa
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