ANKS3 antibody (AbBy Fluor® 555)
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- Target See all ANKS3 Antibodies
- ANKS3 (Ankyrin Repeat and SAM Domain-Containing Protein 3 (ANKS3))
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Reactivity
- Human, Mouse, Rat
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Host
- Rabbit
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Clonality
- Polyclonal
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Conjugate
- This ANKS3 antibody is conjugated to AbBy Fluor® 555
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Application
- Immunofluorescence (Paraffin-embedded Sections) (IF (p))
- Cross-Reactivity
- Human, Mouse, Rat
- Purification
- Purified by Protein A.
- Immunogen
- KLH conjugated synthetic peptide derived from human ANKS3
- Isotype
- IgG
- Top Product
- Discover our top product ANKS3 Primary Antibody
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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
- ANKS3 (Ankyrin Repeat and SAM Domain-Containing Protein 3 (ANKS3))
- Alternative Name
- ANKS3 (ANKS3 Products)
- Synonyms
- 2700067D09Rik antibody, C81345 antibody, mKIAA1977 antibody, RGD1305833 antibody, ankyrin repeat and sterile alpha motif domain containing 3 antibody, anks3 antibody, ANKS3 antibody, Anks3 antibody
- Background
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Synonyms: Ankyrin repeat and SAM domain containing protein 3, Ankyrin repeat and sterile alpha mot domain containing 3, KIAA1977, ANKS3_HUMAN.
Background: ANKS3 is a 656 amino acid protein that contain six ANK repeats and one SAM (sterile alpha motif) domain. The gene encoding ANKS3 maps to human chromosome 16. Chromosome 16, which is associated with a variety of genetic disorders, encodes over 900 genes and comprises nearly 3 % of the human genome. The GAN gene is located on chromosome 16 and, with mutation, may lead to giant axonal neuropathy, a nervous system disorder characterized by increasing malfunction with growth. The rare disorder Rubinstein-Taybi syndrome is associated with chromosome 16, as is Crohn's disease, which is a gastrointestinal inflammatory condition.
- Gene ID
- 124401
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