KRCC1 Antikörper
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- Target Alle KRCC1 Produkte
- KRCC1 (Lysine-Rich Coiled-Coil 1 (KRCC1))
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Reaktivität
- Human, Maus
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Wirt
- Kaninchen
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Klonalität
- Polyklonal
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Konjugat
- Dieser KRCC1 Antikörper ist unkonjugiert
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Applikation
- Western Blotting (WB), ELISA, Immunohistochemistry (IHC)
- Produktmerkmale
- Polyclonal Antibody
- Aufreinigung
- Antigen affinity purification
- Immunogen
- Fusion protein of human KRCC1
- Isotyp
- IgG
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- Applikationshinweise
- WB 1:500-1:2000, IHC 1:100-1:300, ELISA 1:5000-1:10000
- Beschränkungen
- Nur für Forschungszwecke einsetzbar
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- Format
- Liquid
- Konzentration
- 1.68 mg/mL
- Buffer
- PBS with 0.05 % Sodium azide and 40 % Glycerol, pH 7.4
- Konservierungsmittel
- Sodium azide
- Vorsichtsmaßnahmen
- This product contains Sodium azide: a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.
- Lagerung
- -20 °C
- Informationen zur Lagerung
- Store at -20°C. Avoid freeze / thaw cycles.
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- Target
- KRCC1 (Lysine-Rich Coiled-Coil 1 (KRCC1))
- Andere Bezeichnung
- KRCC1 (KRCC1 Produkte)
- Synonyme
- DKFZp468N1119 antikoerper, CHBP2 antikoerper, AA792894 antikoerper, RGD1306495 antikoerper, lysine rich coiled-coil 1 antikoerper, lysine-rich coiled-coil 1 antikoerper, KRCC1 antikoerper, Krcc1 antikoerper
- Hintergrund
- KRCC1 (lysine-rich coiled-coil 1), also known as CHBP2 (cryptogenic hepatitis-binding protein 2), is a 259 amino acid protein that is encoded by a gene located on human chromosome 2p11.2. Consisting of 237 million bases, chromosome 2 is the second largest human chromosome and encodes over 1,400 genes. 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.
- Molekulargewicht
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Observed_MW: Refer to figures
Calculated_MW: 31 kDa
- UniProt
- Q9NPI7
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