KRCC1 anticorps
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- Antigène Tous les produits KRCC1
- KRCC1 (Lysine-Rich Coiled-Coil 1 (KRCC1))
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Reactivité
- Humain, Souris
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Hôte
- Lapin
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Clonalité
- Polyclonal
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Conjugué
- Cet anticorp KRCC1 est non-conjugé
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Application
- Western Blotting (WB), ELISA, Immunohistochemistry (IHC)
- Attributs du produit
- Polyclonal Antibody
- Purification
- Antigen affinity purification
- Immunogène
- Fusion protein of human KRCC1
- Isotype
- IgG
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- Indications d'application
- WB 1:500-1:2000, IHC 1:100-1:300, ELISA 1:5000-1:10000
- Restrictions
- For Research Use only
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- Format
- Liquid
- Concentration
- 1.68 mg/mL
- Buffer
- PBS with 0.05 % Sodium azide and 40 % Glycerol, pH 7.4
- 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
- -20 °C
- Stockage commentaire
- Store at -20°C. Avoid freeze / thaw cycles.
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- Antigène
- KRCC1 (Lysine-Rich Coiled-Coil 1 (KRCC1))
- Autre désignation
- KRCC1 (KRCC1 Produits)
- Synonymes
- anticorps DKFZp468N1119, anticorps CHBP2, anticorps AA792894, anticorps RGD1306495, anticorps lysine rich coiled-coil 1, anticorps lysine-rich coiled-coil 1, anticorps KRCC1, anticorps Krcc1
- Sujet
- 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.
- Poids moléculaire
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Observed_MW: Refer to figures
Calculated_MW: 31 kDa
- UniProt
- Q9NPI7
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