FASTKD1 Antikörper
Quick Overview for FASTKD1 Antikörper (ABIN7263405)
Target
Reaktivität
Wirt
Klonalität
Konjugat
Applikation
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Produktmerkmale
- Polyclonal Antibody
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Aufreinigung
- Affinity purification
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Immunogen
- Recombinant fusion protein of human FASTKD1 (NP_078898.3).
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Isotyp
- IgG
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anti-FAST Kinase Domains 1 (FASTKD1) (AA 638-847) antibody
FASTKD1 Reaktivität: Human WB Wirt: Kaninchen Polyclonal unconjugated
anti-FAST Kinase Domains 1 (FASTKD1) (AA 2-99) antibodyFASTKD1 Reaktivität: Human ELISA, WB Wirt: Maus Polyclonal unconjugated
anti-FAST Kinase Domains 1 (FASTKD1) antibodyFASTKD1 Reaktivität: Human WB, ICC, IF Wirt: Kaninchen Polyclonal unconjugated
anti-FAST Kinase Domains 1 (FASTKD1) (Internal Region) antibodyFASTKD1 Reaktivität: Human, Maus ELISA, WB, ICC, IF Wirt: Kaninchen Polyclonal unconjugated
anti-FAST Kinase Domains 1 (FASTKD1) (Internal Region) antibodyFASTKD1 Reaktivität: Human, Maus, Affe ELISA, WB Wirt: Kaninchen Polyclonal unconjugated
anti-FAST Kinase Domains 1 (FASTKD1) (AA 561-610) antibodyFASTKD1 Reaktivität: Human, Maus ELISA, WB, IHC, IHC (p) Wirt: Kaninchen Polyclonal unconjugated
anti-FAST Kinase Domains 1 (FASTKD1) (Internal Region) antibodyFASTKD1 Reaktivität: Human, Maus, Affe ELISA, WB Wirt: Kaninchen Polyclonal unconjugated
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Applikationshinweise
- IHC 1:50-1:200
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Beschränkungen
- Nur für Forschungszwecke einsetzbar
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Format
- Liquid
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Konzentration
- 1 mg/mL
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Buffer
- PBS with 0.02 % sodium azide, 50 % glycerol, pH 7.3
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Konservierungsmittel
- Sodium azide
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Vorsichtsmaßnahmen
- This product contains Sodium azide: a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.
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Lagerung
- -20 °C
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Informationen zur Lagerung
- Store at -20°C. Avoid freeze / thaw cycles.
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- FASTKD1 (FAST Kinase Domains 1 (FASTKD1))
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Andere Bezeichnung
- FASTKD1
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Hintergrund
- The second largest human chromosome, 2 consists of 237 million bases encoding over 1,400 genes and making up approximately 8 % of the human genome. A number of genetic diseases are linked to genes on chromosome 2. Harlequin icthyosis, a rare and morbid skin deformity, is associated with mutations in the ABCA12 gene. The lipid metabolic disorder sitosterolemia is associated with ABCG5 and ABCG8. An extremely rare recessive genetic disorder, Alstrm syndrome is due to mutations in the ALMS1 gene. Interestingly, chromosome 2 contains what appears to be a vestigial second centromere and vestigial telomeres which gives credence to the hypothesis that human chromosome 2 is the result of an ancient fusion of two ancestral chromosomes seen in modern form today in apes.
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Gen-ID
- 79675
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UniProt
- Q53R41
Target
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