RBBP8NL Antikörper (AA 21-120) (Biotin)
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- Target Alle RBBP8NL Produkte
- RBBP8NL (RBBP8 N-Terminal Like (RBBP8NL))
- Bindungsspezifität
- AA 21-120
- Reaktivität
- Human
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Wirt
- Kaninchen
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Klonalität
- Polyklonal
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Konjugat
- Dieser RBBP8NL Antikörper ist konjugiert mit Biotin
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Applikation
- Western Blotting (WB), ELISA, Immunohistochemistry (Frozen Sections) (IHC (fro)), Immunohistochemistry (Paraffin-embedded Sections) (IHC (p))
- Homologie
- Human,Mouse,Rat,Cow,Sheep,Pig,Horse,Chicken
- Aufreinigung
- Purified by Protein A.
- Immunogen
- KLH conjugated synthetic peptide derived from human C20orf151
- Isotyp
- IgG
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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
- RBBP8NL (RBBP8 N-Terminal Like (RBBP8NL))
- Andere Bezeichnung
- C20orf151 (RBBP8NL Produkte)
- Synonyme
- C20H20orf151 antikoerper, C20orf151 antikoerper, chromosome 20 C20orf151 homolog antikoerper, RBBP8 N-terminal like antikoerper, C20H20orf151 antikoerper, RBBP8NL antikoerper
- Hintergrund
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Synonyms: C20orf151, Chromosome 20 open reading frame 151, CT151_HUMAN, RP5-908M14.6, Uncharacterized protein C20orf151.
Background: Representing about 2 % of human DNA, chromosome 20 consists of approximately 63 million bases and 600 genes. Chromosome 20 contains a region with numerous genes expressed in the epididymis, which are thought important for seminal production, and some viewed as potential targets for male contraception. The PRNP gene encoding the prion protein associated with spongiform encephalopathies, like Creutzfeldt-Jakob disease, is found on chromosome 20. Amyotrophic lateral sclerosis, spinal muscular atrophy, ring chromosome 20 epilepsy syndrome and Alagille syndrome are also associated with chromosome 20. The C20orf151 gene product has been provisionally designated C20orf151 pending further characterization.
- Gen-ID
- 140893
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