CCDC93 antibody (AA 531-631) (AbBy Fluor® 647)
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- Target See all CCDC93 Antibodies
- CCDC93 (Coiled-Coil Domain Containing 93 (CCDC93))
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Binding Specificity
- AA 531-631
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Reactivity
- Rat
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Host
- Rabbit
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Clonality
- Polyclonal
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Conjugate
- This CCDC93 antibody is conjugated to AbBy Fluor® 647
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Application
- Immunofluorescence (Cultured Cells) (IF (cc)), Immunofluorescence (Paraffin-embedded Sections) (IF (p))
- Cross-Reactivity
- Rat
- Predicted Reactivity
- Human,Mouse,Dog,Cow,Sheep,Pig
- Purification
- Purified by Protein A.
- Immunogen
- KLH conjugated synthetic peptide derived from human CCDC93
- Isotype
- IgG
- Top Product
- Discover our top product CCDC93 Primary Antibody
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- Application Notes
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IF(IHC-P) 1:50-200
IF(IHC-F) 1:50-200
IF(ICC) 1:50-200 - Restrictions
- For Research Use only
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- Format
- Liquid
- Concentration
- 1 μg/μL
- Buffer
- Aqueous buffered solution containing 0.01M TBS ( pH 7.4) with 1 % BSA, 0.03 % Proclin300 and 50 % Glycerol.
- Preservative
- ProClin
- Precaution of Use
- This product contains ProClin: a POISONOUS AND HAZARDOUS SUBSTANCE, which should be handled by trained staff only.
- Storage
- -20 °C
- Storage Comment
- Store at -20°C. Aliquot into multiple vials to avoid repeated freeze-thaw cycles.
- Expiry Date
- 12 months
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- Target
- CCDC93 (Coiled-Coil Domain Containing 93 (CCDC93))
- Alternative Name
- CCDC93 (CCDC93 Products)
- Synonyms
- 4633402D15Rik antibody, 9230102M16Rik antibody, coiled-coil domain containing 93 antibody, coiled-coil domain containing 93 L homeolog antibody, CCDC93 antibody, Ccdc93 antibody, ccdc93.L antibody
- Background
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Synonyms: CCDC 93, Coiled-coil domain containing 93, FLJ10996, FLJ25197, MGC13033, CCD93_HUMAN.
Background: The coiled-coil domain is a structural motif found in proteins that are involved in a diverse array of biological functions such as the regulation of gene expression, cell division, membrane fusion, and drug extrusion and delivery. CCDC93 (coiled-coil domain containing 93) is a 631 amino acid protein that belongs to the CCDC93 family. CCDC93 is encoded by a gene located on human chromosome 2, which makes up approximately 8 % of the human genome and contains 237 million bases encoding over 1,400 genes. A number of genetic diseases are linked to genes on chromosome 2. Harlequin icthyosis, a rare 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, Alstr syndrome, is related to mutations in the ALMS1 gene.
- Gene ID
- 54520
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