Septin 9 anticorps (AA 536-586)
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- Antigène Voir toutes Septin 9 (SEPT9) Anticorps
- Septin 9 (SEPT9)
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Épitope
- AA 536-586
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Reactivité
- Humain
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Hôte
- Lapin
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Clonalité
- Polyclonal
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Conjugué
- Cet anticorp Septin 9 est non-conjugé
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Application
- Western Blotting (WB), Immunoprecipitation (IP), Immunofluorescence (Paraffin-embedded Sections) (IF (p))
- Fonction
- Rabbit anti-Septin 9 Antibody, Affinity Purified
- Purification
- Affinity Purified
- Immunogène
- between AA 536 and 586
- Isotype
- IgG
- Top Product
- Discover our top product SEPT9 Anticorps primaire
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- Indications d'application
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IHC-IF: 1:1,000 - 1:5,000
IP: 2 - 5 μg/mg lysate
WB: Not recommended. Use rabbit anti-Septin 9 antibody ABIN7453779.
- Restrictions
- For Research Use only
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- Concentration
- 1000 μg/mL
- Buffer
- Tris-citrate/phosphate buffer, pH 7 to 8 containing 0.09 % Sodium Azide
- Agent conservateur
- Sodium azide
- Précaution d'utilisation
- This product contains Sodium azide: a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.
- Stock
- 4 °C
- Date de péremption
- 12 months
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- Antigène
- Septin 9 (SEPT9)
- Autre désignation
- Septin 9 (SEPT9 Produits)
- Synonymes
- anticorps SEPT9, anticorps msf, anticorps msf1, anticorps napb, anticorps sint1, anticorps pnutl4, anticorps septd1, anticorps af17q25, anticorps septin-9, anticorps AF17q25, anticorps MSF, anticorps MSF1, anticorps NAPB, anticorps PNUTL4, anticorps SINT1, anticorps SeptD1, anticorps Msf, anticorps Sint1, anticorps Eseptin, anticorps Slpa, anticorps cb999, anticorps fb02h06, anticorps sept9, anticorps wu:fb02h06, anticorps septin 9, anticorps septin-9, anticorps septin 9 S homeolog, anticorps septin 9a, anticorps SEPT9, anticorps sept9, anticorps LOC100605286, anticorps sept9.S, anticorps Sept9, anticorps sept9a
- Sujet
- 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].
- ID gène
- 10801
- NCBI Accession
- NP_001106963
- UniProt
- Q9UHD8
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