KRCC1 antibody
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- Target See all KRCC1 products
- KRCC1 (Lysine-Rich Coiled-Coil 1 (KRCC1))
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Reactivity
- Human, Mouse
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Host
- Rabbit
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Clonality
- Polyclonal
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Conjugate
- This KRCC1 antibody is un-conjugated
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Application
- Western Blotting (WB), ELISA, Immunohistochemistry (IHC)
- Characteristics
- Polyclonal Antibody
- Purification
- Antigen affinity purification
- Immunogen
- Fusion protein of human KRCC1
- Isotype
- IgG
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anti-Lysine-Rich Coiled-Coil 1 (KRCC1) (AA 1-259) antibody
KRCC1 Reactivity: Human ELISA, IF Host: Rabbit Polyclonal unconjugated
anti-Lysine-Rich Coiled-Coil 1 (KRCC1) (AA 35-84) antibodyKRCC1 Reactivity: Human, Horse WB Host: Rabbit Polyclonal unconjugated
anti-Lysine-Rich Coiled-Coil 1 (KRCC1) (N-Term) antibodyKRCC1 Reactivity: Human, Horse WB Host: Rabbit Polyclonal unconjugated
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- Application Notes
- 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
- Preservative
- Sodium azide
- Precaution of Use
- This product contains Sodium azide: a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.
- Storage
- -20 °C
- Storage Comment
- Store at -20°C. Avoid freeze / thaw cycles.
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- Target
- KRCC1 (Lysine-Rich Coiled-Coil 1 (KRCC1))
- Alternative Name
- KRCC1 (KRCC1 Products)
- Synonyms
- DKFZp468N1119 antibody, CHBP2 antibody, AA792894 antibody, RGD1306495 antibody, lysine rich coiled-coil 1 antibody, lysine-rich coiled-coil 1 antibody, KRCC1 antibody, Krcc1 antibody
- Background
- 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.
- Molecular Weight
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Observed_MW: Refer to figures
Calculated_MW: 31 kDa
- UniProt
- Q9NPI7
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