CWF19L1 antibody (AbBy Fluor® 350)
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- Target See all CWF19L1 products
- CWF19L1 (CWF19-Like 1, Cell Cycle Control (CWF19L1))
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Reactivity
- Human, Rat, Mouse
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Host
- Rabbit
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Clonality
- Polyclonal
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Conjugate
- This CWF19L1 antibody is conjugated to AbBy Fluor® 350
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Application
- Western Blotting (WB), Immunofluorescence (Paraffin-embedded Sections) (IF (p))
- Cross-Reactivity
- Human, Mouse, Rat
- Purification
- Purified by Protein A.
- Immunogen
- KLH conjugated synthetic peptide derived from human CWF19L1
- Isotype
- IgG
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- Application Notes
- IF(IHC-P) 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
- CWF19L1 (CWF19-Like 1, Cell Cycle Control (CWF19L1))
- Alternative Name
- CWF19L1 (CWF19L1 Products)
- Synonyms
- 2610528C06Rik antibody, AI854304 antibody, AV336991 antibody, CWF19-like 1, cell cycle control (S. pombe) antibody, CWF19 like 1, cell cycle control (S. pombe) antibody, CWF19 like 1, cell cycle control (S. pombe) L homeolog antibody, Cwf19l1 antibody, CWF19L1 antibody, cwf19l1.L antibody
- Background
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Synonyms: CWF19-like 1, cell cycle control, C19L1_HUMAN.
Background: CWF19L1 is a 538 amino acid protein belonging to the CWF19 family and exists as three alternatively spliced isoforms. CWF19L1 is encoded by a gene located on human chromosome 10, which spans nearly 135 million base pairs, makes up approximately 4.5 % of total DNA in cells and encodes nearly 1,200 genes. Several protein-coding genes, including those that encode for chemokines, cadherins, excision repair proteins, early growth response factors (Egrs) and fibroblast growth receptors (FGFRs), are located on chromosome 10. Defects in some of the genes that map to chromosome 10 are associated with Charcot-Marie Tooth disease, Jackson-Weiss syndrome, Usher syndrome, nonsyndromatic deafness, Wolman?s syndrome, Cowden syndrome, multiple endocrine neoplasia type 2 and porphyria.
- Gene ID
- 55280
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