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Invitrogen™ FAM13B Polyclonal Antibody

Rabbit Polyclonal Antibody

Supplier:  Invitrogen™ PA567216

Catalog No. PIPA567216


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Description

Description

Immunogen sequence: YSLLKFLCRFL ANVASHHEEI WSANSLAAVF GPDVFHIYTD VEDMKEQEIV SRIMAGLLEN YYEFFENEEE DFSSNDLSSI Highest antigen sequence identity to the following orthologs - mouse 100%, rat 100%.

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.
TRUSTED_SUSTAINABILITY
Specifications

Specifications

FAM13B
Polyclonal
Unconjugated
FAM13B
2610024E20Rik; ARHGAP49; AW060714; AW546153; C5orf5; Fam13b; FAM13B1; family with sequence similarity 13 member B; family with sequence similarity 13, member B; family with sequence similarity 13, member B1; GAP-like protein N61; KHCHP; N61; protein FAM13B; RGD1310484
Rabbit
Antigen affinity chromatography
RUO
51306
Store at 4°C short term. For long term storage, store at -20°C, avoiding freeze/thaw cycles.
Liquid
Immunohistochemistry (Paraffin)
0.2 mg/mL
PBS with 40% glycerol and 0.02% sodium azide; pH 7.2
Q9NYF5
FAM13B
Recombinant Human FAM13B. Recombinant protein control fragment (Product #RP-107851).
100 μL
Primary
Human
Antibody
IgG
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