Kelch Repeat And BTB Domain-Containing Protein 3 (KBTBD3) Antibody

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468€ (100 µl)

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935106861
info@markelab.com
name
Kelch Repeat And BTB Domain-Containing Protein 3 (KBTBD3) Antibody
category
Primary Antibodies
provider
Abbexa
reference
abx117232
tested applications
ELISA, WB, IHC

Description

KBTBD3 Antibody is a Rabbit Polyclonal antibody against KBTBD3.

Documents del producto

Instrucciones
Data sheet
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Product specifications

Category
Primary Antibodies
Immunogen Target
Kelch Repeat And BTB Domain-Containing Protein 3 (KBTBD3)
Host
Rabbit
Reactivity
Human, Mouse, Rat
Recommended Dilution
WB: 1/500 - 1/2000, IHC: 1/50 - 1/200. Optimal dilutions/concentrations should be determined by the end user.
Clonality
Polyclonal
Conjugation
Unconjugated
Isotype
IgG
Purification
Purified by affinity chromatography.
Size 1
100 µl
Form
Liquid
Tested Applications
ELISA, WB, IHC
Buffer
PBS, pH 7.3, containing 0.02% sodium azide and 50% glycerol.
Availability
Shipped within 5-10 working days.
Storage
Aliquot and store at -20°C. Avoid repeated freeze/thaw cycles.
Dry Ice
No
UniProt ID
Q8NAB2
Gene ID
143879
Background
Antibody anti-KBTBD3
Status
RUO

Descripción

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Kelch Repeat And BTB Domain-Containing Protein 3 (KBTBD3) Antibody

KBTBD3 Antibody is a Rabbit Polyclonal antibody against KBTBD3. The BTB (Broad-Complex, Tramtrack and Bric a brac) domain, also known as the POZ (Poxvirus and Zinc finger) domain, is an N-terminal homodimerization domain that contains multiple copies of kelch repeats and/or C2H2-type zinc fingers. Proteins that contain BTB domains are thought to be involved in transcriptional regulation via control of chromatin structure and function. KBTBD3 (kelch repeat and BTB domain-containing protein 3), also known as BKLHD3, is a 608 amino acid protein that contains one BACK (BTB/Kelch associated) domain, one BTB (POZ) domain and five kelch repeats. The gene encoding KBTBD3 maps to human chromosome 11, which houses over 1,400 genes and comprises nearly 4% of the human genome. Jervell and Lange-Nielsen syndrome, Jacobsen syndrome, Niemann-Pick disease, hereditary angioedema and Smith-Lemli-Opitz syndrome are associated with defects in genes that maps to chromosome 11.

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