C1orf101 antibody
The Rabbit Polyclonal anti-C1orf101 antibody is suitable to detect C1orf101 in samples from Human. It has been validated for ELISA and IHC.
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Catalog No. ABIN7246079
$480.43
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Quick Overview for C1orf101 antibody (ABIN7246079)
Target
C1orf101 (C1ORF101)
(Chromosome 1 Open Reading Frame 101 (C1ORF101))
Reactivity
Human
Host
Rabbit
Clonality
Polyclonal
Conjugate
This C1orf101 antibody is un-conjugated
Application
ELISA, Immunohistochemistry (IHC)
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Characteristics
- Polyclonal Antibody
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Purification
- Antigen affinity purification
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Immunogen
- Fusion protein of human C1orf101
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Isotype
- IgG
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Application Notes
- IHC 1:50-1:300, ELISA 1:5000-1:10000
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Restrictions
- For Research Use only
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Format
- Liquid
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Concentration
- 1.1 mg/mL
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Buffer
- PBS with 0.05 % Sodium azide and 40 % Glycerol, pH 7.4
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Preservative
- Sodium azide
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Precaution of Use
- This product contains Sodium azide: a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.
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Storage
- -20 °C
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Storage Comment
- Store at -20°C. Avoid freeze / thaw cycles.
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- C1orf101 (C1ORF101) (Chromosome 1 Open Reading Frame 101 (C1ORF101))
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Alternative Name
- C1orf101
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Background
- Chromosome 1 is the largest human chromosome spanning about 260 million base pairs and making up 8 % of the human genome. There are about 3,000 genes on chromosome 1, and considering the great number of genes there are also a large number of diseases associated with chromosome 1. Notably, the rare aging disease Hutchinson-Gilford progeria is associated with the LMNA gene which encodes lamin A. When defective, the LMNA gene product can build up in the nucleus and cause characteristic nuclear blebs. The mechanism of rapidly enhanced aging is unclear and is a topic of continuing exploration. The MUTYH gene is located on chromosome 1 and is partially responsible for familial adenomatous polyposis. Stickler syndrome, Parkinsons, Gaucher disease and Usher syndrome are also associated with chromosome 1. A breakpoint has been identified in 1q which disrupts the DISC1 gene and is linked to schizophrenia. Aberrations in chromosome 1 are found in a variety of cancers including head and neck cancer, malignant melanoma and multiple myeloma. The C1orf101 gene product has been provisionally designated C1orf101 pending further characterization.
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UniProt
- Q5SY80
Target
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