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Thermo Fisher Scientific KBTBD3 Polyclonal Antibody
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Thermo Fisher Scientific KBTBD3 Polyclonal Antibody

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KBTBD3 단백질을 검출하는 Thermo Fisher Scientific의 Rabbit Polyclonal Antibody. Western blot, IHC, ICC/IF 등 다양한 응용에 사용 가능. 인간, 마우스, 랫트 반응성. 고순도 Affinity chromatography 정제 및 안정적인 PBS/glycerol 저장.

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Thermo Fisher Scientific PA5102592 KBTBD3 Polyclonal Antibody 100 ul pk판매 단위 pk
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Thermo Fisher Scientific · Thermo Fisher Scientific KBTBD3 Polyclonal Antibody

Applications

Western Blot (WB)

  • Tested Dilution: 1:500–1:2,000

Immunohistochemistry (Paraffin) (IHC (P))

  • Tested Dilution: 1:50–1:200

Immunocytochemistry (ICC/IF)

  • Tested Dilution: 1:100–1:500

Product Specifications

항목 내용
Species Reactivity Human, Mouse, Rat
Host/Isotype Rabbit / IgG
Class Polyclonal
Type Antibody
Immunogen A synthesized peptide derived from human KBTBD3 (Accession Q8NAB2), corresponding to amino acid residues L507–A557
Conjugate Unconjugated
Form Liquid
Concentration 1 mg/mL
Purification Affinity chromatography
Storage buffer PBS, pH 7.4, with 50% glycerol
Contains 0.02% sodium azide
Storage conditions -20°C
Shipping conditions Wet ice
RRID AB_2851994

Product Specific Information

Antibody detects endogenous levels of total KBTBD3.


Target Information

The BTB (Broad-Complex, Tram track 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 containing BTB domains are 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 on chromosome 11.


For Research Use Only. Not for use in diagnostic procedures. Not for resale without express authorization.

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