BAZ1B Recombinant Rabbit Monoclonal Antibody (JG36-32), Invitrogen™
Manufacturer: Thermo Scientific
Select a Size
| Pack Size | SKU | Availability | Price |
|---|---|---|---|
| Each of 1 | PIMA534748-Each-of-1 | In Stock | ₹ 46,947.50 |
PIMA534748 - Each of 1
In Stock
Quantity
1
Base Price: ₹ 46,947.50
GST (18%): ₹ 8,450.55
Total Price: ₹ 55,398.05
Antigen
BAZ1B
Classification
Monoclonal
Concentration
1 mg/mL
Formulation
TBS with 0.05% BSA, 40% glycerol and 0.05% sodium azide; pH 7.4
Gene Accession No.
Q9UIG0
Gene Symbols
BAZ1B
Immunogen
Recombinant protein within Human WSTF aa 2-96
Quantity
100 μL
Primary or Secondary
Primary
Target Species
Human
Product Type
Antibody
Isotype
IgG
Applications
Flow Cytometry, Western Blot
Clone
JG36-32
Conjugate
Unconjugated
Gene
BAZ1B
Gene Alias
BAZ1B; bromodomain adjacent to zinc finger domain 1B; bromodomain adjacent to zinc finger domain protein 1B; bromodomain adjacent to zinc finger domain, 1B; bromodomain adjacent to zinc finger domain, 1B; Williams-Beuren syndrome chromosome region 9 homolog; C87820; hWALp2; transcription factor WSTF; tyrosine-protein kinase BAZ1B; tyrosine-protein kinase BAZ1B; LOW QUALITY PROTEIN: tyrosine-protein kinase BAZ1B; Tyrosine-protein kinase BAZ1B-like protein; WBSC10; WBSCR10; WBSCR9; williams syndrome transcription factor; Williams syndrome transcription factor homolog; williams-Beuren syndrome chromosomal region 10 protein; Williams-Beuren syndrome chromosomal region 9 protein; williams-Beuren syndrome chromosomal region 9 protein homolog; Williams-Beuren syndrome chromosome region 9 homolog; Wstf
Host Species
Rabbit
Purification Method
Protein A
Regulatory Status
RUO
Gene ID (Entrez)
9031
Content And Storage
-20° C, Avoid Freeze/Thaw Cycles, store in dark
Form
Liquid
Related Products
Description
- Positive Control: SiHa, K562
- BAZ1B is a member of the bromodomain protein family
- The bromodomain is a structural motif characteristic of proteins involved in chromatin-dependent regulation of transcription
- This gene is deleted in Williams-Beuren syndrome, a developmental disorder caused by deletion of multiple genes at 7q11.23.This gene encodes a member of the bromodomain protein family
- The bromodomain is a structural motif characteristic of proteins involved in chromatin-dependent regulation of transcription
- This gene is deleted in Williams-Beuren syndrome, a developmental disorder caused by deletion of multiple genes at 7q11.23.