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Thermo Fisher Scientific LMAN1 Polyclonal Antibody
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Thermo Fisher Scientific LMAN1 Polyclonal Antibody

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LMAN1 단백질을 인식하는 Thermo Fisher Scientific의 토끼 다클론 항체로, Western blot 및 면역형광(ICC/IF)에 적합합니다. 인간, 생쥐, 랫트 시료에서 반응하며, 항원 친화 크로마토그래피로 정제되었습니다. 연구용으로만 사용 가능합니다.

카탈로그번호
PA1074
판매단위
pk
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마지막 업데이트 2025. 08. 02. 오전 01:05
Thermo Fisher Scientific PA1074 LMAN1 Polyclonal Antibody 100 ug pk판매 단위 pk ·
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706,800원VAT 포함 777,480원

Thermo Fisher Scientific · Thermo Fisher Scientific LMAN1 Polyclonal Antibody

Applications and Tested Dilution

Application Tested Dilution Publications
Western Blot (WB) 1:2,000 View 3 publications
Immunocytochemistry (ICC/IF) 1:200 -

Product Specifications

항목 내용
Species Reactivity Human, Mouse, Rat
Published Species Rat
Host / Isotype Rabbit / IgG
Class Polyclonal
Type Antibody
Immunogen Synthetic peptide corresponding to residues F(159) D S F D N D G K K N N P A I(173) of rat ERGIC-53
Conjugate Unconjugated
Form Liquid
Concentration 1 mg/mL
Purification Antigen affinity chromatography
Storage Buffer PBS with 1 mg/mL BSA
Contains 0.05% sodium azide
Storage Conditions -20°C, Avoid Freeze/Thaw Cycles
Shipping Conditions Ambient (domestic); Wet ice (international)
RRID AB_2265708

Product Specific Information

PA1-074 detects ERGIC-53 in rat, mouse, and human samples.
This antibody has been successfully used in Western blot and immunofluorescence (ICC/IF) procedures.
By Western blot, it detects a ~57.5 kDa protein representing ERGIC-53 in rat brain samples.

The immunogen is a synthetic peptide corresponding to residues F(159) D S F D N D G K K N N P A I(173) of rat ERGIC-53, conserved in mouse and human.
The immunizing peptide (Cat. # PEP-277) is available for use in neutralization and control experiments.


Target Information

The LMAN1 protein is a type I integral membrane protein localized in the intermediate region between the endoplasmic reticulum and the Golgi apparatus, recycling between these compartments.
It functions as a mannose-specific lectin and belongs to a family of plant lectin homologs in the secretory pathway of animal cells.
Mutations in this gene are associated with a coagulation defect, specifically combined factor V-factor VIII deficiency, a rare autosomal recessive disorder characterized by reduced levels of both coagulation factors V and VIII.


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

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