PIPA5103333
FAM111B Polyclonal Antibody, Invitrogen™
Manufacturer: Thermo Scientific
Select a Size
| Pack Size | SKU | Availability | Price |
|---|---|---|---|
| Each of 1 | PIPA5103333-Each-of-1 | In Stock | ₹ 46,502.50 |
PIPA5103333 - Each of 1
In Stock
Quantity
1
Base Price: ₹ 46,502.50
GST (18%): ₹ 8,370.45
Total Price: ₹ 54,872.95
Antigen
FAM111B
Classification
Polyclonal
Conjugate
Unconjugated
Gene
FAM111B
Gene Alias
Cancer-associated nucleoprotein; CANP; FAM111B; family with sequence similarity 111 member B; family with sequence similarity 111, member B; POIKTMP; Protein FAM111B
Host Species
Rabbit
Purification Method
Affinity chromatography
Regulatory Status
RUO
Gene ID (Entrez)
374393
Content And Storage
-20°C
Form
Liquid
Applications
Immunocytochemistry, Immunohistochemistry (Paraffin), Western Blot
Concentration
1 mg/mL
Formulation
PBS with 50% glycerol and 0.02% sodium azide; pH 7.4
Gene Accession No.
Q6SJ93
Gene Symbols
FAM111B
Immunogen
A synthesized peptide derived from human FAM111B(Accession Q6SJ93), corresponding to amino acid residues L44-R94.
Quantity
100 μL
Primary or Secondary
Primary
Target Species
Human, Mouse
Product Type
Antibody
Isotype
IgG
Related Products
Description
- Antibody detects endogenous levels of total F111B
- FAM111B is a 734 amino acid protein that is encoded by a gene that maps to human chromosome 11, which makes up around 4% of human genomic DNA and isconsidered a gene and disease association dense chromosome.The chromosome 11 encoded Atmgene isimportant for regulation ofcellcycle arrest and apoptosisfollowing double strand DNA breaks
- Atmmutation leads to the disorderknown as ataxia-telangiectasia
- The blood disorders Sickle cell anemia and beta thalassemia are caused by HBB genemutations
- Wilms' tumors, WAGR syndrome and Denys-Drash syndrome are associatedwithmutations of the WT1 gene
- Jervell and Lange-Nielsen syndrome, Jacobsen syndrome, Niemann-Pick disease, hereditary angioedema and Smith-Lemli-Opitz syndrome are also associatedwith defectsin chromosome 11.