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Western blot analysis in NCI-H460 cell line lysates (35ug/lane).
CHST6 Antibody immunohistochemistry analysis in formalin fixed and paraffin embedded human brain tissue followed by peroxidase conjugation of the secondary antibody and DAB staining.
Western blot analysis in NCI-H460 cell line lysates (35ug/lane).

CHST6 Antibody

CATALOG NUMBER: 56-365

Clonality:
Polyclonal
Tested Applications:
IHC-P, WB
Host Species:
Rabbit
Species Reactivity:
Human
Conjugate:
Unconjugated
Specifications
Host Species:
Rabbit
Species Reactivity:
Human
Immunogen:
This CHST6 antibody is generated from rabbits immunized with a KLH conjugated synthetic peptide between 296-325 amino acids from the C-terminal region of human CHST6.
Conjugate:
Unconjugated
Tested Applications:
IHC-P, WB
Application Note:
For WB starting dilution is: 1:1000
For IHC-P starting dilution is: 1:10~50
Predicted Molecular Weight:
44 kDa
Purification:
This antibody is purified through a protein A column, followed by peptide affinity purification.
Clonality:
Polyclonal
Isotype:
Rabbit Ig
Physical State:
Liquid
Buffer:
Supplied in PBS with 0.09% (W/V) sodium azide.
Concentration:
batch dependent
Storage Conditions:
Store at 4°C for three months and -20°C, stable for up to one year. As with all antibodies care should be taken to avoid repeated freeze thaw cycles. Antibodies should not be exposed to prolonged high temperatures.
Ncbi Official Symbol:
CHST6
Additional Names:
Carbohydrate sulfotransferase 6, 282-, Corneal N-acetylglucosamine-6-O-sulfotransferase, C-GlcNAc6ST, hCGn6ST, Galactose/N-acetylglucosamine/N-acetylglucosamine 6-O-sulfotransferase 4-beta, GST4-beta, N-acetylglucosamine 6-O-sulfotransferase 5, GlcNAc6ST-5, Gn6st-5, CHST6
Protein Accession Number:
Q9GZX3
Ncbi Gene Id Number:
4166
User Note:
Optimal dilutions for each application to be determined by the researcher.
Background:
The protein encoded by this gene is an enzyme thatcatalyzes the transfer of a sulfate group to the GlcNAc residues ofkeratan. Keratan sulfate helps maintain corneal transparency.Defects in this gene are a cause of macular corneal dystrophy(MCD).
Background Reference 1:
Liu, Z., et al. Cornea 29(8):883-888(2010)
Background Reference 2:
Dastani, Z., et al. Eur. J. Hum. Genet. 18(3):342-347(2010)
Background Reference 3:
Dang, X., et al. Mol. Vis. 15, 700-705 (2009) :
Background Reference 4:
Birgani, S.A., et al. Mol. Vis. 15, 373-377 (2009) :

FOR RESEARCH USE ONLY

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

Disclaimer:
Optimal dilutions/concentrations should be determined by the end user. The information provided is a guideline for product use. This product is for research use only.

CATALOG NUMBER:

56-365

List Size:
400 ul

List Price:

$495.00

Datasheet
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