Products for Research Use Only

Rabbit SMARCA2/BRM Antibody

CAT: 0013-GTR18219682-01Size: 10 µLDry Ice: NoHazardous: No
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CAT#:0013-GTR18219682-01Size:10 µL
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Description
SMARCA2/BRM Antibody
Product Name Alternative
ATP-dependent helicase SMARCA2; BAF190; BAF190B; brahma homolog; BRG1-associated factor 190B; BRM; global transcription activator homologous sequence; hBRM; hSNF2a; NCBRS; probable global transcription activator SNF2L2; protein brahma homolog; SNF2; SNF2/SWI2-like protein 2; SNF2-alpha; SNF2L2; SNF2LA; Sth1p; sucrose nonfermenting 2-like protein 2; SWI/SNF-related matrix-associated actin-dependent regulator of chromatin a2; SWI/SNF-related matrix-associated actin-dependent regulator of chromatin subfamily A member 2; SWI2
UniProt
P51531
Reactivity
Human
Immunogen
Between 1 and 50
Target
SMARCA2/BRM
Clonality
Polyclonal
Conjugation
Unconjugated
Field of Research
Neuroscience
Purification
Antigen Affinity Purified
Concentration
200 μg/ml
Dilution
WB - 1:2,000 - 1:10,000; IP - 2 - 5 μg/mg lysate
Form
Liquid
Storage Conditions
2 - 8°C
Notes
For research use only.
Applications Notes
Format: Whole IgG
Tested Applications
IP, WB
NCBI Accession Number
NP_003061.3
Host or Source
Rabbit
Preservative
Tris-buffered Saline containing 0.1% rAlbumin and 0.09% Sodium Azide
Isotype
IgG

UniProtKB · P51531

SWI/SNF-related matrix-associated actin-dependent regulator of chromatin subfamily A member 2

SMCA2_HUMAN · Homo sapiens

View on UniProt ↗
Primary accession
P51531
Review status
UniProtKB reviewed (Swiss-Prot)
Gene
SMARCA2
Protein existence
1: Evidence at protein level
Organism
Homo sapiens (Human)
Taxonomy ID
9606
Alternative names
SAMRCA2
EC number
3.6.4.-
Processing
—
Secondary accessions
B1ALG3, B1ALG4, D3DRH4, D3DRH5
Protein keywords

Technical term

3D-structureProteomics identificationReference proteome

PTM

AcetylationIsopeptide bondPhosphoproteinUbl conjugation

Molecular function

ActivatorDNA-bindingHydrolase

Coding sequence diversity

Alternative splicing

Ligand

ATP-bindingNucleotide-binding

Domain

Bromodomain

Disease

Disease variantHypotrichosisIntellectual disabilitySchizophrenia

Biological process

NeurogenesisTranscriptionTranscription regulation

Cellular component

Nucleus