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Antibody used in IHC on Human kidney at 4.0-8.0 ug/ml.
Antibody used in WB on Human heart at 0.2-1 ug/ml.
Antibody used in IF on Human lymphatic endothelial at 1:50 -1:500.
Antibody used in IHC on Human kidney at 4.0-8.0 ug/ml.

SOX18 Antibody

CATALOG NUMBER: 27-776

Clonality:
Polyclonal
Tested Applications:
ELISA, IHC, WB
Host Species:
Rabbit
Species Reactivity:
Human, Mouse, Rat
Conjugate:
Unconjugated
Specifications
Host Species:
Rabbit
Species Reactivity:
Human, Mouse, Rat
Immunogen:
Antibody produced in rabbits immunized with a synthetic peptide corresponding a region of human SOX18.
Conjugate:
Unconjugated
Tested Applications:
ELISA, IHC, WB
Application Note:
SOX18 antibody can be used for detection of SOX18 by ELISA at 1:62500. SOX18 antibody can be used for detection of SOX18 by western blot at 0.5 μg/mL, and HRP conjugated secondary antibody should be diluted 1:50,000 - 100,000.
Positive Control 1:
Cat. No. XBL-10407 - Fetal Heart Tissue Lysate
Predicted Molecular Weight:
41 kDa
Purification:
Antibody is purified by peptide affinity chromatography method.
Clonality:
Polyclonal
physical-state:
Liquid
Buffer:
Purified antibody supplied in 1x PBS buffer with 0.09% (w/v) sodium azide and 2% sucrose.
Concentration:
batch dependent
Storage Conditions:
For short periods of storage (days) store at 4°C. For longer periods of storage, store SOX18 antibody at -20°C. As with any antibody avoid repeat freeze-thaw cycles.
Ncbi Official Symbol:
SOX18
Additional Names:
SOX18, HLTS
Protein Accession Number:
NP_060889
Protein Gi Number:
8924248
Ncbi Gene Id Number:
54345
User Note:
Optimal dilutions for each application to be determined by the researcher.
Background:
SOX18 is a member of the SOX (SRY-related HMG-box) family of transcription factors involved in the regulation of embryonic development and in the determination of the cell fate. The encoded protein may act as a transcriptional regulator after forming a protein complex with other proteins. This protein plays a role in hair, blood vessel, and lymphatic vessel development. Mutations in this gene have been associated with recessive and dominant forms of hypotrichosis-lymphedema-telangiectasia.
Background Reference 1:
Spataro, V., et al., (2005) Arterioscler. Thromb. Vasc. Biol. 25 (11), 2398-2403.

FOR RESEARCH USE ONLY

For additional information, visit ProSci’s Terms & Conditions Page.

Disclaimer:
This product is for research use only.

CATALOG NUMBER:

27-776

List Size:
100 ul

List Price:

$519.00

Datasheet
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