FAM13B antibody
FAM13B
Reactivity: Human, Mouse
ELISA, IHC
Host: Rabbit
Polyclonal
unconjugated
-
- Target See all FAM13B products
- FAM13B (Family with Sequence Similarity 13, Member B (FAM13B))
- Reactivity
- Human, Mouse
-
Host
- Rabbit
-
Clonality
- Polyclonal
-
Conjugate
- This FAM13B antibody is un-conjugated
-
Application
- ELISA, Immunohistochemistry (IHC)
- Characteristics
- Polyclonal Antibody
- Purification
- Affinity purification
- Immunogen
- Synthetic peptide of human FAM13B
- Isotype
- IgG
-
anti-Family with Sequence Similarity 13, Member B (FAM13B) (AA 566-594) antibody
FAM13B Reactivity: Human WB Host: Rabbit Polyclonal RB31467 unconjugated
anti-Family with Sequence Similarity 13, Member B (FAM13B) (AA 1-915) antibodyFAM13B Reactivity: Human WB Host: Mouse Polyclonal unconjugated
-
- Application Notes
- IHC 1:50-1:200
- Restrictions
- For Research Use only
-
- Format
- Liquid
- Concentration
- 0.4 mg/mL
- Buffer
- PBS with 0.05 % sodium azide and 50 % glycerol, PH7.4
- Preservative
- Sodium azide
- Precaution of Use
- This product contains Sodium azide: a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.
- Storage
- -20 °C
- Storage Comment
- Store at -20°C. Avoid freeze / thaw cycles.
-
- Target
- FAM13B (Family with Sequence Similarity 13, Member B (FAM13B))
- Alternative Name
- FAM13B (FAM13B Products)
- Synonyms
- ARHGAP49 antibody, C5orf5 antibody, FAM13B1 antibody, KHCHP antibody, N61 antibody, 2610024E20Rik antibody, AW060714 antibody, AW546153 antibody, family with sequence similarity 13 member B antibody, family with sequence similarity 13, member B antibody, FAM13B antibody, Fam13b antibody
- 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.
- NCBI Accession
- NP_057687
- UniProt
- Q9NYF5
-
You are here:
