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Product Name LYSMD3 Chinese Name LYSMD3蛋白抗体 Alias 1110030H10Rik; BC003322; lysM and putative peptidoglycan binding domain containing protein 3; LysM and putative peptidoglycan-binding domain-containing protein 3; LYSM3_HUMAN; lysmd3; RGD1308805. Research Area Cell biology immunology Immunogen Species Rabbit Clonality Polyclonal React Species (predicted: Human, Mouse, Rat, Dog, Pig, Cow, Horse, Sheep, ) Applications ELISA=1:5000-10000 IHC-P=1:100-500 IHC-F=1:100-500 ICC=1:100-500 IF=1:100-500 (Paraffin sections need antigen repair)
not yet tested in other applications.
optimal dilutions/concentrations should be determined by the end user.Theoretical molecular weight 34kDa Cellular localization The cell membrane Form Liquid Concentration 1mg/ml immunogen KLH conjugated synthetic peptide derived from human LYSMD3: 1-100/306 <Extracellular> Lsotype IgG Purification affinity purified by Protein A Buffer Solution 0.01M TBS(pH7.4) with 1% BSA, 0.03% Proclin300 and 50% Glycerol. Storage Shipped at 4℃. Store at -20 °C for one year. Avoid repeated freeze/thaw cycles. Attention This product as supplied is intended for research use only, not for use in human, therapeutic or diagnostic applications. PubMed PubMed Product Detail LYSMD3 is a 306 amino acid single-pass membrane protein that contains one LysM repeat and exists as three alternatively spliced isoforms. The gene encoding LYSMD3 maps to human chromosome 5q14.3. With 181 million base pairs encoding around 1,000 genes, chromosome 5 is about 6% of human genomic DNA. It is associated with Cockayne syndrome through the ERCC8 gene and familial adenomatous polyposis through the adenomatous polyposis coli (APC) tumor suppressor gene. Treacher Collins syndrome is also chromosome 5 associated and is caused by insertions or deletions within the TCOF1 gene. Deletion of the p arm of chromosome 5 leads to Cri du chat syndrome. Deletion of 5q or chromosome 5 altogether is common in therapy-related acute myelogenous leukemias and myelodysplastic syndrome.
Subcellular Location:
Membrane.
Similarity:
Contains 1 LysM repeat.
SWISS:
Q7Z3D4
Gene ID:
116068
Database links:Entrez Gene: 116068 Human
SwissProt: Q7Z3D4 Human
Unigene: 136235 Human
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