推薦產品
生物源
rabbit
共軛
unconjugated
抗體表格
affinity isolated antibody
抗體產品種類
primary antibodies
無性繁殖
polyclonal
形狀
buffered aqueous solution
分子量
antigen ~23 kDa
物種活性
mouse, human, rat
技術
indirect immunofluorescence: 5-10 μg/mL using rat NRK and mouse NIH-3T3 cells fixed and permeabilized with 3% paraformaldehyde followed by 0.4% saponin
western blot: 2.5-5.0 μg/mL using extract of human A431 cells
UniProt登錄號
運輸包裝
dry ice
儲存溫度
−20°C
目標翻譯後修改
unmodified
基因資訊
human ... RAB7A(7879)
mouse ... Rab7(19349)
rat ... Rab7a(29448)
一般說明
Rab7 is a member of the Rab family of small guanosine triphosphatases (GTPases). Rab proteins contain conserved regions involved in guanine nucleotide binding, and hypervariable COOH-terminal domains with a cysteine motif, implicated in subcellular targeting. Each Rab protein shows a characteristic subcellular distribution. The antibody is affinity-purified using the immunizing peptide immobilized on agarose.
Ras-related protein Rab-7 (Rab7) is a member of the Rab family of small guanosine triphosphatases (GTPases).
特異性
Anti- Rab7 recognizes human, mouse and rat Rab7.
免疫原
Synthetic peptide corresponding to amino acid residues of human Rab7 with C-terminal added cysteine, conjugated to KLH.
應用
Anti-Rab7 antibody can be used in indirect immunofluorescence and immunoblotting.
Anti-Rab7 antibody produced in rabbit has been used in confocal microscopy.
生化/生理作用
Rab family of small guanosine triphosphatases (GTPases) are central regulators of membrane trafficking between the different subcellular compartments of the eukaryotic cell. Their regulatory capacity depends on their ability to cycle between the GDP-bound inactive and GTP-bound active states. Conversion from one state to the other is regulated by GDP/GTP exchange factors (GEPs), GDP dissociation inhibitors (GDIs) and GTPase-activating proteins (GAPs). Activation of a Rab protein is coupled to its association with intracellular membranes, allowing it to recruit downstream effector proteins to the cytoplasmic surface of a subcellular compartment. Through their effector proteins, Rab GTPases regulate vesicle formation, actin- and tubulin-dependent vesicle movement, and membrane fusion. Rab7 is also involved in the maturation of late autophagic vacuoles. Among Rab7 effectors are RILP (Rab-interacting lysosome protein) that controls late endosomal and lysosomal transport by mediating the recruitment of dynein/dynactin motors, Rabring7 (Rab7- interacting ring finger protein),(10) and the hVPS34/p150 complex. Anti-Rab7 may be used as a marker for late endosomes.
外觀
0.01M 磷酸缓冲盐溶液,pH 7.4,含 15mM 叠氮化钠。
儲存和穩定性
For continuous use, store at 2-8 °C for up to one month. For extended storage freeze in working aliquots. Repeated freezing and thawing is not recommended. If slight turbidity occurs upon prolonged storage, clarify the solution by centrifugation before use. Working dilution samples should be discarded if not used within 12 hours.
免責聲明
Unless otherwise stated in our catalog or other company documentation accompanying the product(s), our products are intended for research use only and are not to be used for any other purpose, which includes but is not limited to, unauthorized commercial uses, in vitro diagnostic uses, ex vivo or in vivo therapeutic uses or any type of consumption or application to humans or animals.
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儲存類別代碼
10 - Combustible liquids
水污染物質分類(WGK)
WGK 3
閃點(°F)
Not applicable
閃點(°C)
Not applicable
分析證明 (COA)
輸入產品批次/批號來搜索 分析證明 (COA)。在產品’s標籤上找到批次和批號,寫有 ‘Lot’或‘Batch’.。
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Role for Rab7 in maturation of late autophagic vacuoles
Journal of Cell Science, 117(20), 4837-4848 (2004)
Rab7 and Rab9 are recruited onto late endosomes by biochemically distinguishable processes
The Journal of Biological Chemistry, 270(43), 25541-25548 (1995)
IL-7 induces clathrin-mediated endocytosis of CD127 and subsequent degradation by the proteasome in primary human CD8 T cells
Immunology and Cell Biology, 94(2), 196-207 (2016)
Human VPS34 and p150 are Rab7 interacting partners
Traffic, 4(11), 754-771 (2003)
Structural basis for recruitment of RILP by small GTPase Rab7
The Embo Journal, 24(8), 1491-1501 (2005)
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