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GRHL2 Antibody (HRP)

CAT: 0013-GTR17900809-01Size: 50 µgDry Ice: NoHazardous: No
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CAT#:0013-GTR17900809-01Size:50 µg
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24/48H Stock Items & 2 to 6 Weeks non Stock Items.
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Description
This GRHL2 Antibody, HRP conjugated is an HRP polyclonal product. It tagets GRHL2 using a Recombinant Human Grainyhead-like protein 2 homolog protein (1-265AA) as the immunogen. This antibody is suitable for ELISA. Purification: Antigen Affinity Purified.
Product Name Alternative
BOM antibody; Brother of mammalian grainyhead antibody; Deafness autosomal dominant 28 antibody; DFNA28 antibody; ECTDS antibody; FLJ11172 antibody; FLJ13782 antibody; Grainyhead like 2 (Drosophila) antibody; Grainyhead like 2 antibody; Grainyhead like protein 2 homolog antibody; Grainyhead like transcription factor 2 antibody; Grainyhead-like protein 2 homolog antibody; GRHL 2 antibody; GRHL2 antibody; GRHL2_HUMAN antibody; MGC149294 antibody; MGC149295 antibody; RGD1561191 antibody; TFCP2L3 antibody; Transcription factor CP2 like 3 antibody; Transcription factor CP2-like 3 antibody
UniProt
Q6ISB3
Reactivity
Human
Immunogen
Recombinant Human Grainyhead-like protein 2 homolog protein (1-265AA)
Target
GRHL2
Clonality
Polyclonal
Conjugation
HRP
Field of Research
Neuroscience
Purification
>95%, Protein G purified
Dilution
ELISA
Form
Liquid
Storage Conditions
Upon receipt, store at -20°C or -80°C. Avoid repeated freeze.
Notes
For research use only.
Tested Applications
ELISA
Host or Source
Rabbit
Preservative
Preservative: 0.03% Proclin 300. Constituents: 50% Glycerol
Isotype
IgG

UniProtKB · Q6ISB3

Grainyhead-like protein 2 homolog

GRHL2_HUMAN · Homo sapiens

View on UniProt ↗
Primary accession
Q6ISB3
Review status
UniProtKB reviewed (Swiss-Prot)
Gene
GRHL2
Protein existence
1: Evidence at protein level
Organism
Homo sapiens (Human)
Taxonomy ID
9606
Alternative names
—
EC number
—
Processing
—
Secondary accessions
A1L303, Q6NT03, Q9H8B8
Protein keywords

Technical term

3D-structureProteomics identificationReference proteome

Molecular function

ActivatorDNA-binding

Coding sequence diversity

Alternative splicing

Disease

Corneal dystrophyDeafnessDisease variantDwarfismEctodermal dysplasiaNon-syndromic deafness

Cellular component

MembraneNucleus

Biological process

TranscriptionTranscription regulation

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