RAB23 Mouse mAb (一抗) - WB,Flow-Cyt,ELISA | Bioss

2026-05-01~2026-06-30,AB2605
货号:bsm-51516M
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概述

产品编号
bsm-51516M
英文名称
RAB23 Mouse mAb
中文名称
G蛋白偶联受体RAB23单克隆抗体
英文别名
HSPC137; opb; opb2; rab-15; RAB23_HUMAN; RAB23; 3.6.5.2; RAB23, member RAS oncogene family
抗体来源
Mouse
免疫原
Recombinant human RAB23 (Fragment) (His-tagged).
亚型
IgG1
性状
Liquid
纯化方法
affinity purified by Protein G
克隆类型
Monoclonal
克隆号
G6S4
理论分子量
23 kDa
浓度
1mg/ml
储存液
0.01M TBS (pH7.4) with 1% BSA, 0.02% Proclin300 and 50% Glycerol.
SWISS
Gene ID
保存条件
Shipped at 4℃. Store at -20℃ for one year. Avoid repeated freeze/thaw cycles.
注意事项
This product as supplied is intended for research use only, not for use in human, therapeutic or diagnostic applications.
背景资料
The Ras-related superfamily of guanine nucleotide binding proteins includes the R-Ras, Rap, Ral/Rec and Rho/Rab subfamilies. Increasing data suggests an important role for Rab proteins in either endocytosis or in biosynthetic protein transport. The process of transporting newly synthesized proteins from the endoplasmic reticulum to various stacks of the Golgi complex and to secretory vesicles involves the movement of carrier vesicles and requires Rab protein function. Rab proteins are also an integral part of endocytic pathways. Rab 23, also known as HSPC137, is a 237 amino acid member of the Rab family of proteins and localizes to the cytoplasmic side of the cell membrane. Rab 23 is believed to play a role in intracellular protein transportation and signal transduction mediated by small GTPases. Mutations in the gene encoding Rab 23 may result in Carpenter syndrome, also known as ACPS2 (acrocephalopolysyndactyly type 2), a condition characterized by obesity, cardiac defects, polysyndactyly and craniosynostosis.

产品应用

应用已检合格种属预测种属推荐稀释比例
WBHuman, Mouse1:500-2000
Flow-CytHuman, Mouse1:50-100
ELISAHuman, Mouse1:5000-10000

交叉反应

交叉反应: Human, Mouse

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靶标

基因名
RAB23
蛋白名
Ras-related protein Rab-23
亚基
Interacts with SUFU.
亚细胞定位
Cell membrane; Lipid-anchor; Cytoplasmic side. Cell membrane. Cytoplasm. Cytoplasmic vesicle, autophagosome. Endosome membrane. Cytoplasmic vesicle, phagosome. Cytoplasmic vesicle, phagosome membrane; Lipid-anchor; Cytoplasmic side. Note=Recruited to phagosomes containing S.aureus or M.tuberculosis.
疾病
Defects in RAB23 are the cause of acrocephalopolysyndactyly type 2 (ACPS2) [MIM:201000]. A syndrome characterized by craniosynostosis, polysyndactyly, obesity, and cardiac defects.
相似性
Belongs to the small GTPase superfamily. Rab family.
功能
The small GTPases Rab are key regulators of intracellular membrane trafficking, from the formation of transport vesicles to their fusion with membranes. Rabs cycle between an inactive GDP-bound form and an active GTP-bound form that is able to recruit to membranes different set of downstream effectors directly responsible for vesicle formation, movement, tethering and fusion. Together with SUFU, prevents nuclear import of GLI1, and thereby inhibits GLI1 transcription factor activity. Regulates GLI1 in differentiating chondrocytes. Likewise, regulates GLI3 proteolytic processing and modulates GLI2 and GLI3 transcription factor activity. Plays a role in autophagic vacuole assembly, and mediates defense against pathogens, such as S.aureus, by promoting their capture by autophagosomes that then merge with lysosomes.

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