CCDC112 antibody
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- Target See all CCDC112 Antibodies
- CCDC112 (Coiled-Coil Domain Containing 112 (CCDC112))
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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 CCDC112 antibody is un-conjugated
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Application
- ELISA, Immunohistochemistry (IHC)
- Characteristics
- Polyclonal Antibody
- Purification
- Antigen affinity purification
- Immunogen
- Fusion protein of human CCDC112
- Isotype
- IgG
- Top Product
- Discover our top product CCDC112 Primary Antibody
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anti-Coiled-Coil Domain Containing 112 (CCDC112) (AA 201-446) antibody
CCDC112 Reactivity: Human ELISA, WB, IHC, IF Host: Rabbit Polyclonal unconjugated
anti-Coiled-Coil Domain Containing 112 (CCDC112) (AA 71-120) antibodyCCDC112 Reactivity: Human, Mouse, Rat, Bat, Cow, Dog, Monkey WB, IHC, IHC (p) Host: Rabbit Polyclonal unconjugated
anti-Coiled-Coil Domain Containing 112 (CCDC112) (AA 1-30), (N-Term) antibodyCCDC112 Reactivity: Human WB Host: Rabbit Polyclonal RB37835 unconjugated
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- Application Notes
- IHC 1:40-1:200, ELISA 1:5000-1:10000
- Restrictions
- For Research Use only
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- Format
- Liquid
- Concentration
- 0.5 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
- CCDC112 (Coiled-Coil Domain Containing 112 (CCDC112))
- Alternative Name
- CCDC112 (CCDC112 Products)
- Synonyms
- CCDC112 antibody, RGD1561942 antibody, MBC1 antibody, 8430438M01Rik antibody, AW108467 antibody, coiled-coil domain containing 112 antibody, CCDC112 antibody, Ccdc112 antibody, ccdc112 antibody
- Background
- CCDC112 (coiled-coil domain containing 112), also known as MBC1 (mutated in bladder cancer 1), is a 446 amino acid protein. The gene encoding CCDC112 is located on chromosome 5. Due to alternative splicing events, CCDC112 exists as two isoforms. Chromosome 5 comprises about 6 % of human genomic DNA and contains 181 million base pairs encoding around 1,000 genes. It is associated with Cockayne syndrome through the ERCC8 gene and familial adenomatous polyposis through the adenomatous polyposis coli (APC) tumor suppressor gene. Treacher Collins syndrome is also chromosome 5 associated and is caused by insertions or deletions within the TCOF1 gene. Deletion of the p arm of chromosome 5 leads to Cri du chat syndrome. Deletion of 5q or chromosome 5 altogether is common in therapy-related acute myelogenous leukemias and myelodysplastic syndrome.
- UniProt
- Q8NEF3
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