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Thermo Fisher Scientific CSH1 Monoclonal Antibody (OTI1C9)
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Thermo Fisher Scientific CSH1 Monoclonal Antibody (OTI1C9)

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CSH1 단백질을 인식하는 Mouse IgG2a 단일클론 항체로, Western blot, IHC, ICC/IF 등 다양한 응용에 적합. 고순도 Affinity Chromatography 정제, 1 mg/mL 농도. 인간 시료 반응성, 연구용으로만 사용.

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마지막 업데이트 2025. 08. 04. 오전 03:18
Thermo Fisher Scientific MA526275 CSH1 Monoclonal Antibody (OTI1C9) 100 ul pk판매 단위 pk ·
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775,200원VAT 포함 852,720원

Thermo Fisher Scientific · Thermo Fisher Scientific CSH1 Monoclonal Antibody (OTI1C9)

Applications

Application Tested Dilution
Western Blot (WB) 1:1,000
Immunohistochemistry (Paraffin) (IHC (P)) 1:150
Immunocytochemistry (ICC/IF) Assay-Dependent

Product Specifications

항목 내용
Species Reactivity Human
Host / Isotype Mouse / IgG2a
Class Monoclonal
Type Antibody
Clone OTI1C9
Immunogen Full length human recombinant protein of CSH1 produced in HEK293T cell
Conjugate Unconjugated
Form Liquid
Concentration 1 mg/mL
Purification Affinity Chromatography
Storage Buffer PBS, pH 7.3, with 1% BSA, 50% glycerol
Contains 0.02% sodium azide
Storage Conditions -20°C, Avoid Freeze/Thaw Cycles
Shipping Conditions Ambient (domestic); Wet ice (international)
RRID AB_2723018

Target Information

The protein encoded by this gene is a member of the somatotropin/prolactin family of hormones and plays an important role in growth control. The gene is located at the growth hormone locus on chromosome 17 along with four other related genes in the same transcriptional orientation; an arrangement thought to have evolved by a series of gene duplications. Although the five genes share a remarkably high degree of sequence identity, they are expressed selectively in different tissues. Alternative splicing generates additional isoforms, leading to further diversity and specialization. This particular family member is expressed mainly in the placenta and utilizes multiple transcription initiation sites. Expression of the identical mature proteins for chorionic somatomammotropin hormones 1 and 2 is upregulated during development, although the ratio of 1 to 2 increases by term. Mutations in this gene result in placental lactogen deficiency and Silver-Russell syndrome.

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

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