Product Name
HYLS1, Polyclonal Antibody
Popular Item
Full Product Name
HYLS1 Polyclonal Antibody
Product Gene Name
anti-HYLS1 antibody
[Similar Products]
Research Use Only
For Research Use Only. Not for use in diagnostic procedures.
3D Structure
ModBase 3D Structure for Q96M11
Purity/Purification
Affinity Purification
Immunogen
Recombinant Protein
Immunogen
Recombinant protein of human HYLS1
Preparation and Storage
Store at -20 degree C. Avoid freeze / thaw cycles.
Buffer: PBS with 0.02% sodium azide, 50% glycerol, pH7.3.
Other Notes
Small volumes of anti-HYLS1 antibody vial(s) may occasionally become entrapped in the seal of the product vial during shipment and storage. If necessary, briefly centrifuge the vial on a tabletop centrifuge to dislodge any liquid in the container`s cap. Certain products may require to ship with dry ice and additional dry ice fee may apply.
Related Product Information for
anti-HYLS1 antibody
This gene encodes a protein localized to the cytoplasm. Mutations in this gene are associated with hydrolethalus syndrome. Multiple alternatively spliced variants, encoding the same protein, have been identified.
Applications Tested/Suitable for anti-HYLS1 antibody
Western Blot (WB)
Application Notes for anti-HYLS1 antibody
WB 1:500 - 1:2000
Western Blot (WB) of anti-HYLS1 antibody
Western blot analysis of extracts of MCF-7 cells, using HYLS1 antibody at 1:1000 dilution.
Secondary antibody: HRP Goat Anti-Rabbit IgG (H+L) (MBS128200) at 1:10000 dilution.
Lysates/proteins: 25ug per lane.
Blocking buffer: 3% nonfat dry milk in TBST.
Detection: ECL Basic Kit.
Exposure time: 90s.

NCBI/Uniprot data below describe general gene information for HYLS1. It may not necessarily be applicable to this product.
NCBI Accession #
NP_001128265.1
[Other Products]
NCBI GenBank Nucleotide #
NM_001134793.1
[Other Products]
UniProt Primary Accession #
Q96M11
[Other Products]
UniProt Secondary Accession #
Q96BX9; B3KXI8[Other Products]
UniProt Related Accession #
Q96M11[Other Products]
NCBI Official Full Name
hydrolethalus syndrome protein 1
NCBI Official Synonym Full Names
hydrolethalus syndrome 1
NCBI Official Symbol
HYLS1??[Similar Products]
NCBI Official Synonym Symbols
HLS
??[Similar Products]
NCBI Protein Information
hydrolethalus syndrome protein 1
UniProt Protein Name
Hydrolethalus syndrome protein 1
Protein Family
Hydrolethalus syndrome protein
UniProt Gene Name
HYLS1??[Similar Products]
UniProt Synonym Gene Names
HLS??[Similar Products]
UniProt Entry Name
HYLS1_HUMAN
NCBI Summary for HYLS1
This gene encodes a protein localized to the cytoplasm. Mutations in this gene are associated with hydrolethalus syndrome. Multiple alternatively spliced variants, encoding the same protein, have been identified. [provided by RefSeq, Oct 2008]
UniProt Comments for HYLS1
HYLS1: Defects in HYLS1 are the cause of hydrolethalus syndrome type 1 (HLS1). HLS1 is a lethal malformation syndrome leading to stillbirth or death shortly after birth. It is characterized by hydrocephaly with absent upper midline structures of the brain, micrognathia and polydactyly. Belongs to the HYLS1 family.
Protein type: Unknown function
Chromosomal Location of Human Ortholog: 11q24.2
Cellular Component: centrosome; cytoplasm; plasma membrane; nucleus
Disease: Hydrolethalus Syndrome 1
Research Articles on HYLS1
1. Clinical trial of gene-disease association and gene-environment interaction. (HuGE Navigator)
Precautions
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Disclaimer
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