Home > Product > Antibody > Rabbit Anti-CHST14 antibody
2600016L03Rik; ATCS; Carbohydrate (N acetylgalactosamine 4 0) sulfotransferase 14; Carbohydrate sulfotransferase 14; CHST14; CHSTE_HUMAN; D4ST-1; D4st1; Dermatan 4-sulfotransferase 1; hD4ST1; RP23-286G12.2; UNQ1925/PRO4400.
Cat:
SL13933R
Species Reactivity:
Mouse,Rat,(predicted: Human,Dog,Pig,Cow,Horse,Sheep,)
Immunogen:
KLH conjugated synthetic peptide derived from human CHST14:201-300/376
Format:
Liquid
Storage instructions:
Shipped at 4℃. Store at -20 °C for one year. Avoid repeated freeze/thaw cycles.
Concentration:
1mg/ml
Clonality:
Polyclonal
Isotype:
IgG
Applications:
WB=1:500-2000ELISA=1:5000-10000not yet tested in other applications.optimal dilutions/concentrations should be determined by the end user.
Host:
Rabbit
Product Overview:
Sample:Ovary (Mouse) Lysate at 40 ugPrimary: Anti- CHST14 (SL13933R)at 1/300 dilutionSecondary: IRDye800CW Goat Anti-Rabbit IgG at 1/20000 dilutionPredicted band size: 43kDObserved band size: 43kD
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Unit:
Price: $
Product PDFs
Datasheet:


This gene encodes a member of the HNK-1 family of sulfotransferases. The encoded protein transfers sulfate to the SLC4 hydroxyl of N-acetylgalactosamine residues in dermatan sulfate. Mutations in this gene have been associated with adducted thumb-clubfoot syndrome.[provided by RefSeq, Mar 2010]

Function:
Catalyzes the transfer of sulfate to position 4 of the N-acetylgalactosamine (GalNAc) residue of dermatan sulfate. Transfers sulfate to the SLC4 hydroxyl of beta1,4-linked GalNAc that is substituted with an alpha-linked iduronic acid (IdoUA) at the SLC3 hydroxyl. Transfers sulfate more efficiently to GalNAc residues in -IdoUA-GalNAc-IdoUA- than in -GlcUA-GalNAc-GlcUA-sequences. Has preference for partially desulfated dermatan sulfate. Addition of sulfate to GalNAc may occur immediately after epimerization of GlcUA to IdoUA.

Subcellular Location:
Golgi apparatus membrane.

Tissue Specificity:
Widely expressed. Expressed at high level in pituitary gland, placenta, uterus and thyroid.

DISEASE:
Defects in CHST14 are the cause of Ehlers-Danlos syndrome musculocontractural type (EDSMC) [MIM:601776]. It is a form of Ehlers-Danlos syndrome characterized by distinctive craniofacial dysmorphism, congenital contractures of thumbs and fingers, clubfeet, severe kyphoscoliosis, muscular hypotonia, hyperextensible thin skin with easy bruisability and atrophic scarring, wrinkled palms, joint hypermobility, and ocular involvement.

Similarity:
Belongs to the sulfotransferase 2 family.

SWISS:
Q8NCH0

Gene ID:
113189

Database links:

Entrez Gene: 113189 Human

Entrez Gene: 72136 Mouse

Omim: 608429 Human

SwissProt: Q8NCH0 Human

SwissProt: Q80V53 Mouse

Unigene: 442449 Human

Unigene: 278349 Mouse

Unigene: 48484 Mouse



Picture

Sample:
Ovary (Mouse) Lysate at 40 ug
Primary: Anti- CHST14 (SL13933R)at 1/300 dilution
Secondary: IRDye800CW Goat Anti-Rabbit IgG at 1/20000 dilution
Predicted band size: 43kD
Observed band size: 43kD
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