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Rabbit HELLS Antibody

CAT: 0013-GTR18220407-02Size: 100 µLDry Ice: NoHazardous: No
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CAT#:0013-GTR18220407-02Size:100 µL
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24/48H Stock Items & 2 to 6 Weeks non Stock Items.
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Description
HELLS Antibody
Product Name Alternative
ICF4; LSH; lymphoid-specific helicase; Nbla10143; PASG; proliferation-associated SNF2-like protein; SMARCA6; SWI/SNF2-related matrix-associated actin-dependent regulator of chromatin subfamily A member 6; SWI/SNF2-related, matrix-associated, actin-dependent regulator of chromatin, subfamily A, member 6
UniProt
Q9NRZ9
Reactivity
Human
Immunogen
Between 550 and 600
Target
HELLS
Clonality
Polyclonal
Conjugation
Unconjugated
Field of Research
Stem Cell & Developmental Biology
Purification
Antigen Affinity Purified
Concentration
1000 μg/ml
Dilution
WB - 1:2,000 - 1:10,000; Note: Extra bands of equal intensity may be observed when using orb1530509 for WB of cell lysate.; IP - 2 - 4 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_060533.2
Host or Source
Rabbit
Preservative
Tris-citrate/phosphate buffer, pH 7 to 8 containing 0.09% Sodium Azide
Isotype
IgG

UniProtKB · Q9NRZ9

Lymphoid-specific helicase

HELLS_HUMAN · Homo sapiens

View on UniProt ↗
Primary accession
Q9NRZ9
Review status
UniProtKB reviewed (Swiss-Prot)
Gene
HELLS
Protein existence
1: Evidence at protein level
Organism
Homo sapiens (Human)
Taxonomy ID
9606
Alternative names
LSH
EC number
3.6.4.-
Processing
—
Secondary accessions
B2RB41, Q3LID1, Q6I7N7, Q76H76, Q76H77, Q76H78, Q76H79, Q76H80, Q76H81, Q7Z397, Q7Z5X2, Q8N6P4, Q9H4P5
Protein keywords

Technical term

3D-structureProteomics identificationReference proteome

Coding sequence diversity

Alternative splicing

Ligand

ATP-bindingNucleotide-binding

Biological process

Cell cycleCell divisionMitosisTranscriptionTranscription regulation

Cellular component

ChromosomeNucleus

Domain

Coiled coil

Molecular function

Developmental proteinHelicaseHydrolase

Disease

Disease variant

PTM

Phosphoprotein

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