C9orf21 Antikörper (AA 101-200) (Biotin)
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- Target Alle C9orf21 (AAED1) Antikörper anzeigen
- C9orf21 (AAED1) (AhpC/TSA Antioxidant Enzyme Domain Containing 1 (AAED1))
- Bindungsspezifität
- AA 101-200
- Reaktivität
- Human
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Wirt
- Kaninchen
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Klonalität
- Polyklonal
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Konjugat
- Dieser C9orf21 Antikörper ist konjugiert mit Biotin
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Applikation
- Western Blotting (WB), Immunohistochemistry (Frozen Sections) (IHC (fro)), Immunohistochemistry (Paraffin-embedded Sections) (IHC (p)), ELISA
- Homologie
- Human,Mouse,Rat,Cow,Sheep,Pig,Horse,Rabbit
- Aufreinigung
- Purified by Protein A.
- Immunogen
- KLH conjugated synthetic peptide derived from human C9orf21
- Isotyp
- IgG
- Top Product
- Discover our top product AAED1 Primärantikörper
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- Applikationshinweise
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WB 1:300-5000
IHC-P 1:200-400
IHC-F 1:100-500 - Beschränkungen
- Nur für Forschungszwecke einsetzbar
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- Format
- Liquid
- Konzentration
- 1 μg/μL
- Buffer
- Aqueous buffered solution containing 0.01M TBS ( pH 7.4) with 1 % BSA, 0.03 % Proclin300 and 50 % Glycerol.
- Konservierungsmittel
- ProClin
- Vorsichtsmaßnahmen
- This product contains ProClin: a POISONOUS AND HAZARDOUS SUBSTANCE, which should be handled by trained staff only.
- Lagerung
- -20 °C
- Informationen zur Lagerung
- Store at -20°C for 12 months.
- Haltbarkeit
- 12 months
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- Target
- C9orf21 (AAED1) (AhpC/TSA Antioxidant Enzyme Domain Containing 1 (AAED1))
- Andere Bezeichnung
- C9orf21 (AAED1 Produkte)
- Synonyme
- C9orf21 antikoerper, 1110018J18Rik antikoerper, AI849003 antikoerper, C8H9orf21 antikoerper, AhpC/TSA antioxidant enzyme domain containing 1 antikoerper, AAED1 antikoerper, Aaed1 antikoerper, aaed1 antikoerper
- Hintergrund
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Synonyms: C9orf21, AAED1_HUMAN, RP11-392G7.2, UPF0308 protein C9orf21.
Background: C9orf21 (chromosome 9 open reading frame 21) is a 226 amino acid protein that belongs to the UPF0308 family and is encoded by a gene that maps to human chromosome 9q22.33. Chromosome 9 consists of about 145 million bases, represents 4 % of the human genome and encodes nearly 900 genes. Thought to play a role in gender determination, deletion of the distal portion of 9p can lead to development of male to female sex reversal, the phenotype of a female with a male X,Y genotype. Hereditary hemorrhagic telangiectasia, which is characterized by harmful vascular defects, is associated with the chromosome 9 gene encoding endoglin protein, ENG. Familial dysautonomia is also associated with chromosome 9 though through the gene IKBKAP. Notably, chromosome 9 encompasses the largest interferon family gene cluster. Chromosome 9 is partnered with chromosome 22 in the translocation leading to the aberrant production of BCR-ABL fusion protein often found in leukemias.
- Gen-ID
- 195827
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