KBTBD3 Polyclonal Antibody, Invitrogen™
Manufacturer: Thermo Scientific
Select a Size
| Pack Size | SKU | Availability | Price |
|---|---|---|---|
| Each of 1 | PIPA5102592-Each-of-1 | In Stock | ₹ 46,502.50 |
PIPA5102592 - Each of 1
In Stock
Quantity
1
Base Price: ₹ 46,502.50
GST (18%): ₹ 8,370.45
Total Price: ₹ 54,872.95
Antigen
KBTBD3
Classification
Polyclonal
Conjugate
Unconjugated
Gene
KBTBD3
Gene Alias
2200003A07Rik; Bklhd3; BTB and kelch domain containing 3; BTB and kelch domain-containing protein 3; Kbtbd3; kelch repeat and BTB (POZ) domain containing 3; kelch repeat and BTB domain containing 3; kelch repeat and BTB domain-containing protein 3
Host Species
Rabbit
Purification Method
Affinity chromatography
Regulatory Status
RUO
Gene ID (Entrez)
143879, 315394, 69149
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.
Q8BHI4, Q8NAB2
Gene Symbols
KBTBD3
Immunogen
A synthesized peptide derived from human KBTBD3(Accession Q8NAB2), corresponding to amino acid residues L507-A557.
Quantity
100 μL
Primary or Secondary
Primary
Target Species
Human, Mouse, Rat
Product Type
Antibody
Isotype
IgG
Related Products
Description
- Antibody detects endogenous levels of total KBTBD3
- The BTB (Broad-Complex, Tram track and Bric a brac) domain, also known as the POZ (Poxvirus and Zinc finger) domain, is an N-terminal homodimerization domain that contains multiple copies of kelch repeats and/or C2H2-type zinc fingers
- Proteins that contain BTB domains are thought to be involved in transcriptional regulation via control of chromatin structure and function
- KBTBD3 (kelch repeat and BTB domain-containing protein 3), also known as BKLHD3, is a 608 amino acid protein that contains one BACK (BTB/Kelch associated) domain, one BTB (POZ) domain and five kelch repeats
- The gene encoding KBTBD3 maps to human chromosome 11, which houses over 1,400 genes and comprises nearly 4% of the human genome
- Jervell and Lange-Nielsen syndrome, Jacobsen syndrome, Niemann-Pick disease, hereditary angioedema and Smith-Lemli-Opitz syndrome are associated with defects in genes that maps to chromosome 11.