FAM13B Polyclonal Antibody
Product Specifications
Background
FAM13B is a 915 amino acid protein that is encoded by a gene that maps 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.
Abbreviation
FAM13B
UniProt
Q9NYF5
Host
Rabbit
Reactivity
Human; Mouse
Immunogen
Synthetic peptide of human FAM13B
Target
ARHGAP49; C5orf5; FA13B; Fam13b; FAM13B1; Family with sequence similarity 13 member B; Family with sequence similarity 13; member B1; GAP-like protein N61; KHCHP; N61; Protein FAM13B
Clonality
Polyclonal
Conjugation
Unconjugated
Applications
IHC
Field of Research
Cancer; Cell biology; Signal transduction
Purification
Affinity purification
Concentration
0.4 mg/mL
Dilution
IHC 1:50-1:200
Buffer
PBS with 0.05% sodium azide and 50% glycerol, PH7.4
Shipping Conditions
The product is shipped with ice pack, upon receipt, store it immediately at the temperature recommended.
Storage Conditions
Store at -20°C Valid for 12 months. Avoid freeze / thaw cycles.
Product Datasheet
https://789.bio/ea/ope5vh
Product MSDS
https://789.bio/eb/Hu9WPG
Isotype
IgG
Available Sizes
Curated Selection
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