CacheBy
Thermo Fisher Scientific STAC3 Polyclonal Antibody
원본

Thermo Fisher Scientific STAC3 Polyclonal Antibody

상품 한눈에 보기

STAC3 단백질을 인식하는 Thermo Fisher Scientific의 rabbit polyclonal antibody로, Western blot에 적합합니다. 고순도(>95%) 항원 친화 크로마토그래피로 정제되었으며, 인간·생쥐·랫드 반응성을 가집니다. 장기 보관 시 -20°C에서 안정적으로 유지됩니다.

판매단위
pk
카탈로그 보기

카탈로그

1개 옵션
회원가입 없이 바로 구매하세요
가입하지 않아도 비회원가로 구매하실 수 있습니다.
마지막 업데이트 2025. 08. 02. 오전 07:26
Thermo Fisher Scientific PA575753 STAC3 Polyclonal Antibody 100 ul pk판매 단위 pk ·
재고 확인 필요
642,300원VAT 포함 706,530원

Thermo Fisher Scientific · Thermo Fisher Scientific STAC3 Polyclonal Antibody

Applications

  • Western Blot (WB): 1:500–1:1,000 dilution

Product Specifications

항목 내용
Species Reactivity Rat, Human, Mouse
Host / Isotype Rabbit / IgG
Class Polyclonal
Type Antibody
Immunogen Synthetic peptide corresponding to residues in Human STAC3
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_2719481

Product Specific Information

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

Target Information

The Src homology 3 (SH3) domain is a conserved 60 amino acid protein domain organized into a beta-barrel fold with five or six beta strands forming two tightly packed anti-parallel beta sheets. This domain mediates assembly of protein complexes and interacts with proline-rich regions.
STAC3 (SH3 and cysteine rich domain 3) is a 364 amino acid protein containing one phorbol-ester/DAG-type zinc finger and two SH3 domains. It exists as two alternatively spliced isoforms and maps to human chromosome 12q13.3.
Chromosome 12 encodes over 1,400 genes (~4.5% of the human genome) and is associated with various diseases such as hypochondrogenesis, achondrogenesis, Kniest dysplasia, Noonan syndrome, and trisomy 12p, which causes facial developmental defects and seizure disorders.


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

Thermo Fisher Scientific 상품 둘러보기

전체보기

문의

0

아직 등록된 문의가 없어요.