Products for Research Use Only

Huntingtin/HTT Rabbit Polyclonal Antibody

CAT: 0013-GTR18315870Size: 100 µgDry Ice: NoHazardous: No
Product image 1
1 / 1
CAT#:0013-GTR18315870Size:100 µg
Selected
24/48H Stock Items & 2 to 6 Weeks non Stock Items.
Quick Request Actions
Description
Anti-Huntingtin/HTT Antibody. Tested in ELISA, IHC applications. This antibody reacts with Human.
Product Name Alternative
HD; HD protein; HTT; huntingtin; Huntington disease protein; IT15
UniProt
P42858
Reactivity
Human
Cross Reactivity
No cross reactivity with other proteins.
Immunogen
E.coli-derived human Huntingtin/HTT recombinant protein (Position: R3079-C3142) . Human HTT shares 93.8% and 92.2% amino acid (aa) sequence identity with mouse and rat HTT, respectively.
Target
Huntingtin
Clonality
Polyclonal
Conjugation
Unconjugated
Field of Research
Cell Biology, Signal Transduction
Purification
Immunogen affinity purified.
Concentration
Adding 0.2 ml of distilled water will yield a concentration of 500 μg/ml.
Dilution
Immunohistochemistry (Paraffin-embedded Section), 2-5 μg/ml, Human ELISA, 0.1-0.5 μg/ml
Form
Lyophilized
Molecular Weight
65 kDa
Storage Conditions
Maintain refrigerated at 2-8°C for up to 2 weeks. For long term storage store at -20°C in small aliquots to prevent freeze-thaw cycles.
Notes
For research use only.
Tested Applications
ELISA, IHC
Host or Source
Rabbit
Preservative
Each vial contains 4 mg Trehalose, 0.9 mg NaCl, 0.2 mg Na2HPO4.
Isotype
IgG

UniProtKB · P42858

Huntingtin

HD_HUMAN · Homo sapiens

View on UniProt ↗
Primary accession
P42858
Review status
UniProtKB reviewed (Swiss-Prot)
Gene
HTT
Protein existence
1: Evidence at protein level
Organism
Homo sapiens (Human)
Taxonomy ID
9606
Alternative names
—
EC number
—
Processing
—
Secondary accessions
Q9UQB7
Protein keywords

Technical term

3D-structureProteomics identificationReference proteome

PTM

AcetylationLipoproteinMyristatePhosphoproteinUbl conjugation

Biological process

Apoptosis

Cellular component

CytoplasmCytoplasmic vesicleEndosomeNucleus

Disease

Disease variantIntellectual disabilityNeurodegeneration

Domain

Repeat

Coding sequence diversity

Triplet repeat expansion