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Thermo Fisher Scientific RhoV Polyclonal Antibody
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Thermo Fisher Scientific RhoV Polyclonal Antibody

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Rabbit polyclonal antibody against human RhoV protein. Suitable for IHC (Paraffin) applications with 1:50–1:200 dilution. Unconjugated, purified by antigen affinity chromatography. Stored in PBS with 40% glycerol and sodium azide. For research use only.

판매단위
pk
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마지막 업데이트 2025. 08. 03. 오후 11:56
Thermo Fisher Scientific PA562781 RhoV Polyclonal Antibody 100 ul pk판매 단위 pk ·
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799,600원VAT 포함 879,560원

Thermo Fisher Scientific · Thermo Fisher Scientific RhoV Polyclonal Antibody

Applications

Tested Dilution

  • Immunohistochemistry (Paraffin) (IHC (P)): 1:50–1:200

Product Specifications

항목 내용
Species Reactivity Human
Host / Isotype Rabbit / IgG
Class Polyclonal
Type Antibody
Immunogen Recombinant protein corresponding to Human RhoV. Recombinant protein control fragment (Product #RP-104211).
Conjugate Unconjugated
Form Liquid
Concentration 0.2 mg/mL
Purification Antigen affinity chromatography
Storage Buffer PBS, pH 7.2, with 40% 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_2646544

Product Specific Information

  • Immunogen sequence: KEVFDSAILS AIEHKARLEK KLNAKGVRTL SRCRWKKFFC FV
  • Highest antigen sequence identity to orthologs: Mouse - 100%, Rat - 100%.

Target Information

The Rho subfamily of Ras-related GTPases regulates various cellular functions such as cytoskeletal rearrangement, nuclear signaling, and cell growth.
RhoV (ras homolog gene family, member V), also known as Rho GTPase-like protein ARHV, CHP, or WRCH2 (Wnt-1 responsive Cdc42 homolog 2), is a 236 amino acid protein that controls the actin cytoskeleton through activation of the JNK pathway.
RhoV functions as a lipid anchor at the cytoplasmic side of the cell membrane and is expressed in placenta, pancreas, and fetal brain. It is implicated in cell transformation and encoded by a gene located on human chromosome 15, which houses over 700 genes and comprises nearly 3% of the human genome.
Diseases such as Angelman syndrome, Prader-Willi syndrome, Tay-Sachs disease, and Marfan syndrome are associated with defects in chromosome 15-localized genes.


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

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