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About This Item
UNSPSC Code:
12352203
NACRES:
NA.41
eCl@ss:
32160702
Conjugate:
unconjugated
Clone:
3D9.1, monoclonal
Application:
ICC, WB
Citations:
-
biological source
mouse
Quality Level
conjugate
unconjugated
antibody form
purified immunoglobulin
antibody product type
primary antibodies
clone
3D9.1, monoclonal
species reactivity
human, mouse
technique(s)
immunocytochemistry: suitable, western blot: suitable
isotype
IgG2bκ
NCBI accession no.
UniProt accession no.
shipped in
ambient
target post-translational modification
unmodified
Gene Information
human ... ARID1B(57492)
General description
AT-rich interactive domain-containing protein 1B (UniProt: Q8NFD5; also known as ARID domain-containing protein 1B, BRG1-associated factor 250b, BAF250B, BRG1-binding protein hELD/OSA1, Osa homolog 2, hOsa2, p250R) is encoded by the ARID1B (also known as BAF250B, DAN15, KIAA1235, OSA2) gene (Gene ID: 57492) in human. ARID domain-containing protein 1B (ARID1B) is widely expressed with high levels in heart, skeletal muscle, and kidney. Four isoform of ARID1B have been reported that are produced by alternative splicing. Its ARID domain is localized to amino acids 1053-1144. ARID1B is a component of the SWI/SNF chromatin remodeling complex and may play a role in cell-cycle activation. It is involved in transcriptional activation and repression of select genes by chromatin remodeling (alteration of DNA-nucleosome topology). ARID1B and ARID1A display about 60% homology, but have been reported to have opposing functions in cell cycle arrest and are mutually exclusive since individual SWI/SNF chromatin remodeling complexes can contain either ARID1A or ARID1B, but not both. ARID1B belongs to the neural progenitors-specific chromatin remodeling complex (npBAF complex) and the neuron-specific chromatin remodeling complex (nBAF complex). During neural development a switch from a stem/progenitor to a post-mitotic chromatin remodeling mechanism occurs as neurons exit the cell cycle and become committed to their adult state. Mutations in ARID1B gene are linked to the development of Coffin-Siris syndrome 1, a congenital multiple malformation syndrome with intellectual disability, coarse facial features, and malformations of the cardiac, gastrointestinal, genitourinary, and/or central nervous systems.
~300 kDa observed; 236.12 kDa calculated. Uncharacterized bands may be observed in some lysate(s).
Immunogen
GST/His-tagged recombinant fragment corresponding to 138 amino acids from the N-terminal half of human AT-rich interactive domain-containing protein 1B.
Application
Anti-ARID1B, clone 3D9.1, Cat. No. MABN2266, is a highly specific mouse monoclonal antibody that targets AT-rich interactive domain-containing protein 1B and has been tested for use in Immunocytochemistry and Western Blotting.
Immunocytochemistry Analysis: A 1:250 dilution from a representative lot detected ARID1B in HeLa, A431, HUVEC and NIH/3T3 cells.
Biochem/physiol Actions
Clone 3D9.1 detects AT-rich interactive domain-containing protein 1B (ARID1B) in human and murine cells. It targets an epitope within 138 amino acids from the N-terminal half.
Physical form
Format: Purified
Analysis Note
Evaluated by Western Blotting in HeLa cell lysate.
Western Blotting Analysis: A 1:1,000 dilution of this antibody detected ARID1B in 10 µg of HeLa cell lysate.
Western Blotting Analysis: A 1:1,000 dilution of this antibody detected ARID1B in 10 µg of HeLa cell lysate.
Other Notes
Concentration: Please refer to lot specific datasheet.
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Storage Class
12 - Non Combustible Liquids
wgk
WGK 1
flash_point_f
Not applicable
flash_point_c
Not applicable
Certificates of Analysis (COA)
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Global Trade Item Number
| SKU | GTIN |
|---|---|
| MABN2266 | 04054839412370 |