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SMRD1 rabbit pAb

CAT: 0855-ES10771-02Size: 100 µLDry Ice: NoHazardous: No
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CAT#:0855-ES10771-02Size:100 µL
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Background
The protein encoded by this gene is a member of the SWI/SNF family of proteins, whose members display helicase and ATPase activities and which are thought to regulate transcription of certain genes by altering the chromatin structure around those genes. The encoded protein is part of the large ATP-dependent chromatin remodeling complex SNF/SWI and has sequence similarity to the yeast Swp73 protein. Two transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Jul 2008]
Description
The protein encoded by this gene is a member of the SWI/SNF family of proteins, whose members display helicase and ATPase activities and which are thought to regulate transcription of certain genes by altering the chromatin structure around those genes. The encoded protein is part of the large ATP-dependent chromatin remodeling complex SNF/SWI and has sequence similarity to the yeast Swp73 protein. Two transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Jul 2008],
UniProt
Q96GM5
Swiss Prot
Q96GM5
Reactivity
Human; Mouse
Immunogen
Synthesized peptide derived from part region of human protein AA range: 268-318
Clonality
Polyclonal
Source
Rabbit
Applications
WB; ELISA
Concentration
1 mg/ml
Dilution
WB 1:500-2000 ELISA 1:5000-20000
Molecular Weight
56kD
Storage Conditions
-20°C/1 year
Observed Molecular Weight
56kD
Fragment
IgG
Subcellular Location
Nucleus .
Gene ID (Human)
6602

UniProtKB · Q96GM5

SWI/SNF-related matrix-associated actin-dependent regulator of chromatin subfamily D member 1

SMRD1_HUMAN · Homo sapiens

View on UniProt ↗
Primary accession
Q96GM5
Review status
UniProtKB reviewed (Swiss-Prot)
Gene
SMARCD1
Protein existence
1: Evidence at protein level
Organism
Homo sapiens (Human)
Taxonomy ID
9606
Alternative names
—
EC number
—
Processing
—
Secondary accessions
A6NN27, Q92924, Q9Y635
Protein keywords

Technical term

3D-structureProteomics identificationReference proteome

PTM

AcetylationIsopeptide bondMethylationPhosphoproteinUbl conjugation

Coding sequence diversity

Alternative splicing

Molecular function

Chromatin regulator

Domain

Coiled coil

Disease

Disease variantIntellectual disability

Biological process

Neurogenesis

Cellular component

Nucleus

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SMRD1 rabbit pAb | 0855-ES10771-02 | Gentaur