Suprabasin antibody
The Mouse Monoclonal anti-Suprabasin antibody is suitable to detect Suprabasin in samples from Human. It has been validated for IHC (p).
Catalog No. ABIN7882393
$640.46
Plus shipping costs $50.00
100 μg
Shipping to:
United States
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Quick Overview for Suprabasin antibody (ABIN7882393)
Target
Suprabasin (SBSN)
Reactivity
Human
Host
Mouse
Clonality
Monoclonal
Conjugate
This Suprabasin antibody is un-conjugated
Application
Immunohistochemistry (Paraffin-embedded Sections) (IHC (p))
Grade
Carrier-free
Clone
SBSN-7961
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Purpose
- SBSN Antibody / Suprabasin (azide and preservative free)
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Purification
- Protein A/G affinity
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Immunogen
- A recombinant fragment from the human protein was used as the immunogen for the SBSN antibody.
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Isotype
- IgG1, kappa
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anti-Suprabasin (SBSN) (AA 434-590) antibody
SBSN Reactivity: Human WB Host: Rabbit Polyclonal unconjugated
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Application Notes
- Optimal dilution of the SBSN antibody should be determined by the researcher.
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Restrictions
- For Research Use only
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Format
- Liquid
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Concentration
- 1 mg/mL
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Buffer
- 1 mg/mL in 1X PBS, BSA free, sodium azide free
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Preservative
- Azide free
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Storage
- -20 °C
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Storage Comment
- Aliquot the SBSN antibody and store frozen at -20oC or colder. Avoid repeated freeze-thaw cycles.
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- Suprabasin (SBSN)
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Alternative Name
- SBSN
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Background
- Suprabasin (SBSN) is a 247 amino acid secreted protein that is upregulated in differentiating keratinocytes and is though to play a role in epidermal differentiation. Expressed in uterus, skin, thymus and esophagus, suprabasin is encoded by a gene that maps to human chromosome 19q13.12. Chromosome 19 consists of about 63 million bases with over 1,400 genes, making up over 2 % of human genomic DNA. Chromosome 19 is the genetic home for a number of immunoglobulin superfamily members, including the killer cell and leukocyte Ig-like receptors, a number of ICAMs, the CEACAM and PSG families, and Fca receptors. Key genes for eye color and hair color also map to chromosome 19. Peutz-Jeghers syndrome, spinocerebellar ataxia type 6, the stroke disorder CADASIL, hypercholesterolemia and Insulin-dependent diabetes have been linked to chromosome 19.
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UniProt
- Q6UWP8
Target
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