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Thermo Fisher Scientific SGOL1 Polyclonal Antibody
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Thermo Fisher Scientific SGOL1 Polyclonal Antibody

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SGOL1 단백질을 인식하는 Thermo Fisher Scientific의 Rabbit Polyclonal Antibody로, 인간·마우스·랫트에 반응합니다. Western blot, ICC/IF, ELISA에 적합하며 고순도 Affinity Chromatography로 정제되었습니다. 연구용으로만 사용됩니다.

카탈로그번호
PA5120429
판매단위
pk
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마지막 업데이트 2025. 08. 05. 오전 10:27
Thermo Fisher Scientific PA5120429 SGOL1 Polyclonal Antibody 100 ul pk판매 단위 pk ·
재고 확인 필요
710,700원VAT 포함 781,770원

Thermo Fisher Scientific · Thermo Fisher Scientific SGOL1 Polyclonal Antibody

Thermo Fisher Scientific SGOL1 Polyclonal Antibody

Applications and Tested Dilution

Application Tested Dilution
Western Blot (WB) 1:500–1:2,000
Immunocytochemistry (ICC/IF) 1:50–1:200
ELISA 1 µg/mL

Product Specifications

Specification Description
Species Reactivity Human, Mouse, Rat
Host / Isotype Rabbit / IgG
Class Polyclonal
Type Antibody
Immunogen Recombinant fusion protein containing a sequence corresponding to amino acids 10–100 of human SGOL1 (NP_612493.1)
Conjugate Unconjugated
Form Liquid
Concentration 2.06 mg/mL
Purification Affinity Chromatography
Storage Buffer PBS, pH 7.3, with 50% glycerol
Contains 0.01% thimerosal
Storage Conditions −20°C, Avoid Freeze/Thaw Cycles
Shipping Conditions Wet ice
RRID AB_2914001

Product Specific Information

Positive test controls include: A-549, HT-29, Mouse testis, Rat testis.
The target is usually found in the following locations: Chromosome, Cytoplasm, Nucleus, Centromere, Centrosome, Cytoskeleton, Kinetochore, Microtubule organizing center, Spindle pole.

Immunogen sequence:
SFQDSLEDIK KRMKEKRNKN LAEIGKRRSF IAAPCQIITN TSTLLKNYQD NNKMLVLALE NEKSKVKEAQ DIILQLRKEC YYLTCQLYAL K

Target Information

The protein encoded by this gene is a member of the shugoshin family of proteins. It protects centromeric cohesin from cleavage during mitotic prophase by preventing phosphorylation of a cohesin subunit. Reduced expression leads to premature loss of centromeric cohesion, mis-segregation of sister chromatids, and mitotic arrest.
Evidence suggests protection of cohesin along chromosome arms during mitotic prophase. An isoform lacking exon 6 plays a role in centriole cohesion. Mutations are associated with Chronic Atrial and Intestinal Dysrhythmia (CAID) syndrome, characterized by Sick Sinus Syndrome (SSS) and Chronic Intestinal Pseudo-obstruction (CIPO). Fibroblast cells from CAID patients show increased proliferation and senescence. Pseudogenes exist on chromosomes 1 and 7. Alternative splicing results in multiple transcript variants.

Safety Information

WARNING: This product can expose you to chemicals including mercury, known to cause birth defects or other reproductive harm.
For more information, visit www.P65Warnings.ca.gov.

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

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