FAM13B Polyclonal Antibody
| Code | Size | Price |
|---|
| E-AB-16425-20uL | 20uL | £125.00 |
Quantity:
| E-AB-16425-60uL | 60uL | £172.00 |
Quantity:
| E-AB-16425-120uL | 120uL | £237.00 |
Quantity:
| E-AB-16425-200uL | 200uL | £344.00 |
Quantity:
Prices exclude any Taxes / VAT
Overview
Host Type: Rabbit
Antibody Isotype: IgG
Antibody Clonality: Polyclonal
Regulatory Status: RUO
Target Species:
- Human
- Mouse
Applications:
- Enzyme-Linked Immunosorbent Assay (ELISA)
- Immunohistochemistry (IHC)
Shipping:
Ice packs
Storage:
-20°C
Further Information
Abbreviation:
FAM13B
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.
Buffer:
PBS with 0.05% sodium azide and 50% glycerol, PH7.4
Concentration:
0.4 mg/mL
Conjugation:
Unconjugated
Dilution:
IHC 1:50-1:200
Immunogen:
Synthetic peptide of human FAM13B
Purification method:
Affinity purification
Target Synonym:
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
UNIProt ID:
Q9NYF5