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FAM13B Rabbit anti-Human, Mouse, Polyclonal, Invitrogen™

Rabbit Polyclonal Antibody

Manufacturer:  Invitrogen PA550659

Catalog No. PA550659


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Description

Description

The antibody detects endogenous levels of total FAM13B protein.

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.
Specifications

Specifications

FAM13B
Polyclonal
Unconjugated
FAM13B
Liquid
FAM13B
Synthetic peptide corresponding to a region derived from internal residues of human family with sequence similarity 13, member B
Antigen affinity chromatography
RUO
Antibody
Polyclonal
Human, Mouse
Immunohistochemistry (Paraffin)
1.3 mg/mL
PBS with 50% glycerol and 0.05% sodium azide; pH 7.3
Q9NYF5, Q8K2H3
C5orf5, FAM13B1
Rabbit
IgG
100 μL
-20°C
Primary
225358, 51306
Documents
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