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

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Thermo Fisher Scientific의 KBTBD3 Polyclonal Antibody는 인간 KBTBD3 단백질을 인식하는 고순도 항체로, Western blot에 적합합니다. 항원 친화 크로마토그래피로 정제되었으며, PBS/glycerol buffer에 보관됩니다. 연구용으로만 사용됩니다.

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마지막 업데이트 2025. 08. 05. 오전 08:35
Thermo Fisher Scientific PA576078 KBTBD3 Polyclonal Antibody 100 ul pk판매 단위 pk ·
재고 확인 필요
731,200원VAT 포함 804,320원

Thermo Fisher Scientific · Thermo Fisher Scientific KBTBD3 Polyclonal Antibody

Applications

  • Western Blot (WB): 1:500–1:2,000

Product Specifications

항목 내용
Species Reactivity Human
Host / Isotype Rabbit / IgG
Class Polyclonal
Type Antibody
Immunogen Recombinant full length Human KBTBD3
Conjugate Unconjugated
Form Liquid
Concentration 1 mg/mL
Purification Antigen affinity chromatography
Storage Buffer PBS, pH 7.2, with 50% glycerol
Contains 0.02% sodium azide
Storage Conditions Store at 4°C short term. For long term storage, store at -20°C, avoiding freeze/thaw cycles.
Shipping Conditions Wet ice
RRID AB_2719805

Product Specific Information

The antibody was affinity-purified from rabbit antiserum by affinity chromatography using epitope-specific immunogen. The purity is >95% (by SDS-PAGE).

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 with 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.
Defects in genes on chromosome 11 are associated with Jervell and Lange-Nielsen syndrome, Jacobsen syndrome, Niemann-Pick disease, hereditary angioedema, and Smith-Lemli-Opitz syndrome.

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

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