CHST6 mouse monoclonal antibody, clone OTI1D1 (formerly 1D1)

Name: CHST6 mouse monoclonal antibody, clone OTI1D1 (formerly 1D1)
SKU: GAM911655
Price: 169 CNY
Availability: InStock

AliasesCHST6

ReactivityDog / Human / Monkey / Mouse

ApplicationsWB

Host / ClonalityMouse / Monoclonal

Lead timeIn stock · ships in 48h

$169/ 50μlIn stock 199 · Ready to ship

50μl$169

100μl$299

Applications & Recommended Dilution

Applications & DilutionRecommended Dilution

Recommended dilution1:500

Reactivity: Dog / Human / Monkey / Mouse
Assay: WB

Product Images

Product ImagesImages

CHST6 mouse monoclonal antibody, clone OTI1D1 (formerly 1D1) 图 1 — Image 1 / 2No text caption for this image

CHST6 mouse monoclonal antibody, clone OTI1D1 (formerly 1D1) 图 2 — Image 2 / 2Western blot analysis of extracts (35ug) from 9 different cell lines by usin g anti-CHST6 monoclonal antibody (HepG2: human; HeLa: human; SVT2: mouse; A549: human; COS7: monkey; Jurkat: human; MDCK: canine; PC12: rat; MCF7: human).

Product Specifications

SpecificationsProduct Specifications

Core Attributes CORE ATTRIBUTES

Species Reactivity: DogHumanMonkeyMouse

Applications: WB

Clone name: OTI1D1

Calculated molecular weight: 43.9 kDa

Immunogen: Human recombinant protein fragment corresponding to amino acids 202-395 of human CHST6 (NP_067628) produced in E.coli.

Isotype: IgG1

Host species: Mouse

Clonality: Monoclonal

Purification method: Affinity Purification

Uniprot-A: Q9GZX3

Recommended Dilution RECOMMENDED DILUTION

WB: 1:500

Product Properties PRODUCT PROPERTIES

Shipping: They are shipped out with dry ice/blue ice unless customers require otherwise

Storage Condition: Store at -20°C PBS (pH 7.3) containing 1% BSA, 50% glycerol and 0.02% sodium azide.Stable for 12 months from date of receipt.

Formulation: Liquid

Storage Buffer: PBS (pH 7.3) containing 1% BSA, 50% glycerol and 0.02% sodium azide.

The protein encoded by this gene is an enzyme that catalyzes the transfer of a sulfate group to the GlcNAc residues of keratan. Keratan sulfate helps maintain corneal transparency. Defects in this gene are a cause of macular corneal dystrophy (MCD). [provided by RefSeq, Jan 2010]