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Thermo Fisher Scientific RAB41 Polyclonal Antibody
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Thermo Fisher Scientific RAB41 Polyclonal Antibody

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RAB41 단백질을 인식하는 Thermo Fisher Scientific의 rabbit polyclonal antibody로, Western blot에 적합합니다. 인간, 생쥐, 랫트 반응성이 있으며, 항원 친화 크로마토그래피로 정제되었습니다. PBS/glycerol buffer에 보관하며 연구용으로만 사용됩니다.

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마지막 업데이트 2025. 08. 04. 오후 05:55
Thermo Fisher Scientific PA575905 RAB41 Polyclonal Antibody 100 ul pk판매 단위 pk ·
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642,300원VAT 포함 706,530원

Thermo Fisher Scientific · Thermo Fisher Scientific RAB41 Polyclonal Antibody

Thermo Fisher Scientific RAB41 Polyclonal Antibody

Applications

  • Western Blot (WB)

Tested Dilution: 1:500–1:1,000
Publications: - [References not provided]


Product Specifications

항목 내용
Species Reactivity Human, Mouse, Rat
Host / Isotype Rabbit / IgG
Class Polyclonal
Type Antibody
Immunogen Synthetic peptide corresponding to residues in Human RAB41
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_2719633

Product Specific Information

The antibody was affinity-purified from rabbit antiserum by affinity chromatography using epitope-specific immunogen, and the purity is >95% (by SDS-PAGE).


Target Information

Rab41 (Ras-related protein Rab-41) is a 222 amino acid protein belonging to the small GTPase superfamily and the Rab family. Members of the Rab family regulate membrane trafficking and cycle between inactive GDP-bound and active GTP-bound states, controlled by GTP hydrolysis-activating proteins (GAPs).
Rab41 can be activated by the GAP protein RN-Tre and localizes to the Golgi complex, participating in protein transport and GTP binding.
It exists as two alternatively spliced isoforms, and the gene encoding Rab41 maps to human chromosome Xq13.1. The X chromosome contains about 153 million base pairs and nearly 1,000 genes. Known X-linked conditions include color blindness, hemophilia, and Duchenne muscular dystrophy, which affect males more frequently due to their single X chromosome.


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

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