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Thermo Fisher Scientific STAC3 Polyclonal Antibody
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Thermo Fisher Scientific STAC3 Polyclonal Antibody

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STAC3 단백질을 인식하는 Thermo Fisher Scientific의 Rabbit Polyclonal 항체로, Western blot 및 SPR 분석에 적합합니다. Human에 반응하며, 0.5 mg/mL 농도의 액상 형태로 제공됩니다. Affinity chromatography로 정제되었으며, -20°C에서 보관합니다.

카탈로그번호
PA571261
판매단위
pk
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마지막 업데이트 2025. 08. 05. 오후 06:40
Thermo Fisher Scientific PA571261 STAC3 Polyclonal Antibody 100 ul pk판매 단위 pk ·
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642,300원VAT 포함 706,530원

Thermo Fisher Scientific · Thermo Fisher Scientific STAC3 Polyclonal Antibody

Applications and Tested Dilution

Application Tested Dilution
Western Blot (WB) 1.0 µg/mL
Surface Plasmon Resonance (SPR) Assay-dependent

Product Specifications

항목 내용
Species Reactivity Human
Host / Isotype Rabbit / IgG
Class Polyclonal
Type Antibody
Immunogen Synthetic peptide directed towards the C-terminal region of human STAC3
Conjugate Unconjugated
Form Liquid
Concentration 0.5 mg/mL
Purification Affinity chromatography
Storage Buffer PBS with 2% sucrose
Contains 0.09% sodium azide
Storage Conditions -20°C, Avoid Freeze/Thaw Cycles
Shipping Conditions Wet ice
RRID AB_2689524

Product Specific Information

This target displays homology in the following species:
Cow: 100%; Dog: 100%; Guinea Pig: 100%; Horse: 100%; Human: 100%; Mouse: 93%; Rabbit: 100%; Rat: 100%

Target Information

The Src homology 3 (SH3) domain is a highly conserved 60 amino acid protein domain organized into a beta-barrel fold of five or six beta strands forming two tightly packed anti-parallel beta sheets.
This domain mediates assembly of specific 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.

Human 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 can cause facial developmental defects and seizure disorders.


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

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