FAM105B Polyclonal Antibody, APC-Cy7 Conjugated
Cat# bs-21613R-APC-Cy7
Size : 100ul
Marca : Bioss
FAM105B Polyclonal Antibody, APC-Cy7 Conjugated
Applications
Reactivity
Overview | |
Catalog # | bs-21613R-APC-Cy7 |
Product Name | FAM105B Polyclonal Antibody, APC-Cy7 Conjugated |
Applications | WB |
Reactivity | Human, Mouse, Rat |
Specifications | |
Conjugation | APC-Cy7 |
Host | Rabbit |
Source | KLH conjugated synthetic peptide derived from human FAM105B |
Clonality | Polyclonal |
Isotype | IgG |
Concentration | 1ug/ul |
Purification | Purified by Protein A. |
Storage Buffer | Aqueous buffered solution containing 0.01M TBS (pH7.4) with 1% BSA, 0.03% Proclin300 and 50% Glycerol. |
Storage Condition | Store at -20°C. Aliquot into multiple vials to avoid repeated freeze-thaw cycles. |
Target | |
Gene ID | Q96BN8 |
Swiss Prot | 90268 |
Synonyms | OTUL_HUMAN; Fam105b; Family with sequence similarity 105, member B; FLJ34884; OTULIN; Protein FAM105B. |
Background | 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. The FAM105B gene product has been provisionally designated FAM105B pending further characterization. |
Application Dilution | |
WB |