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Product Name FAM153B Chinese Name FAM153B蛋白抗体 Alias DKFZp434D115; F153B_HUMAN; FAM153B; Family with sequence similarity 153, member B; Hypothetical protein LOC202134; OTTHUMP00000223257; Protein FAM153B. Research Area Tumour Cell biology immunology Immunogen Species Rabbit Clonality Polyclonal React Species Human, Applications WB=1:500-2000 ELISA=1:5000-10000 IHC-P=1:100-500 IHC-F=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 44kDa Cellular localization The nucleus cytoplasmic Form Liquid Concentration 1mg/ml immunogen KLH conjugated synthetic peptide derived from human FAM153B: 301-387/387 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 FAM153A, FAM153B and FAM153C are 310, 387 and 144 amino acid proteins, respectively, that are encoded by a genes mapping to human chromosome 5. 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.
Similarity:
Belongs to the FAM153 family.
SWISS:
P0C7A2
Gene ID:
202134
Database links:Entrez Gene: 202134 Human
SwissProt: P0C7A2 Human
Unigene: 368516 Human
Unigene: 646912 Human
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