Septin 9 Antikörper (AA 536-586)
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- Target Alle Septin 9 (SEPT9) Antikörper anzeigen
- Septin 9 (SEPT9)
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Bindungsspezifität
- AA 536-586
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Reaktivität
- Human
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Wirt
- Kaninchen
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Klonalität
- Polyklonal
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Konjugat
- Dieser Septin 9 Antikörper ist unkonjugiert
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Applikation
- Immunohistochemistry (IHC), Immunofluorescence (Paraffin-embedded Sections) (IF (p))
- Verwendungszweck
- Rabbit anti-Septin 9 IHC Antibody, Affinity Purified
- Homologie
- Monkey,White-tufted-ear marmoset,Crab-eating macaque
- Aufreinigung
- Affinity Purified
- Immunogen
- Between AA 536 and 586
- Isotyp
- IgG
- Top Product
- Discover our top product SEPT9 Primärantikörper
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- Applikationshinweise
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IHC-IF: 1:50 - 1:500
IHC: 1:100 - 1:500
- Beschränkungen
- Nur für Forschungszwecke einsetzbar
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- Konzentration
- 100 μg/mL
- Buffer
- Tris-buffered Saline containing 0.1 % BSA and 0.09 % 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
- Haltbarkeit
- 12 months
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- Target
- Septin 9 (SEPT9)
- Andere Bezeichnung
- Septin 9 (SEPT9 Produkte)
- Synonyme
- SEPT9 antikoerper, msf antikoerper, msf1 antikoerper, napb antikoerper, sint1 antikoerper, pnutl4 antikoerper, septd1 antikoerper, af17q25 antikoerper, septin-9 antikoerper, AF17q25 antikoerper, MSF antikoerper, MSF1 antikoerper, NAPB antikoerper, PNUTL4 antikoerper, SINT1 antikoerper, SeptD1 antikoerper, Msf antikoerper, Sint1 antikoerper, Eseptin antikoerper, Slpa antikoerper, cb999 antikoerper, fb02h06 antikoerper, sept9 antikoerper, wu:fb02h06 antikoerper, septin 9 antikoerper, septin-9 antikoerper, septin 9 S homeolog antikoerper, septin 9a antikoerper, SEPT9 antikoerper, sept9 antikoerper, LOC100605286 antikoerper, sept9.S antikoerper, Sept9 antikoerper, sept9a antikoerper
- Hintergrund
- Background: Septin 9 is a member of the septin family involved in cytokinesis and cell cycle control. This gene is a candidate for the ovarian tumor suppressor gene. Mutations in this gene cause hereditary neuralgic amyotrophy, also known as neuritis with brachial predilection. A chromosomal translocation involving this gene on chromosome 17 and the MLL gene on chromosome 11 results in acute myelomonocytic leukemia [taken from NCBI GeneID:10801].
- Gen-ID
- 10801
- NCBI Accession
- NP_001106963
- UniProt
- Q9UHD8
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