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Merck
모든 사진(3)

주요 문서

G7295

Sigma-Aldrich

Anti-GM130 (C-terminal) antibody produced in rabbit

affinity isolated antibody, buffered aqueous solution

동의어(들):

Anti-GM130 (Golgi Matrix Protein of 130 kDa), Anti-Golgi Autoantigen, Anti-Golgi Matrix Protein GM 130

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About This Item

MDL number:
UNSPSC 코드:
12352203
NACRES:
NA.41

생물학적 소스

rabbit

Quality Level

결합

unconjugated

항체 형태

affinity isolated antibody

항체 생산 유형

primary antibodies

클론

polyclonal

양식

buffered aqueous solution

분자량

antigen ~130 kDa

종 반응성

mouse, human, rat

기술

immunoprecipitation (IP): 2-4 μg using Hela and 3T3 cell extracts.
indirect immunofluorescence: 0.2-0.4 μg/mL using rat NRK cells
western blot (chemiluminescent): 0.1-0.2 μg/mL using whole extract of rat NRK cells

UniProt 수납 번호

배송 상태

dry ice

저장 온도

−20°C

타겟 번역 후 변형

unmodified

유전자 정보

human ... GOLGA2(2801)
mouse ... Golga2(99412)
rat ... Golga2(64528)

관련 카테고리

일반 설명

Golgi Matrix Protein of 130 kDa (GM130) is a peripheral cytoplasmic protein and is a member of the golgin family of Golgi autoantigens. GM130 is an extended rod-like protein containing coiled-coil domains and is tightly bound to Golgi membranes.

면역원

synthetic peptide corresponding to the C-terminal region of human GM130 with an N-terminal added lysine, conjugated to KLH. The corresponding sequence is identical in rat and mouse GM130.

애플리케이션

Anti-GM130 (C-terminal) antibody can be used in immunoblotting (approx. 130 kDa), indirect immunofluorescence (0.2-0.4 μg/mL using rat NRK cells), and immunoprecipitation (2-4 μg using Hela and 3T3 cell extracts). The antibody can also be used for chemiluminescent western blot (0.1-0.2 μg/mL using whole extract of rat NRK cells).
Anti-GM130 (C-terminal) antibody produced in rabbit has been used in:
  • immunoblotting
  • indirect immunofluorescence
  • immunoprecipitation
  • immunohistochemistry

Applications in which this antibody has been used successfully, and the associated peer-reviewed papers, are given below.
Immunohistochemistry (1 paper)
Western Blotting (1 paper)

생화학적/생리학적 작용

Golgi Matrix Protein of 130 kDa (GM130) is involved in maintaining the structural integrity of the Golgi apparatus and vesicular transport. GM130 also interacts with Golgi reassembly-stacking protein of 65 kDa (GRASP65) and participated in postmitotic reassembly and stacking of the Golgi cisternae. The protein along with p115 and GRASP65 might acts as a template in nucleating the formation of the Golgi apparatus. GM130 in complex with GRASP65 and other proteins interacts with activated Rab1, a protein known to regulate the transport of newly synthesized proteins from the endoplasmic reticulum (ER) to the Golgi apparatus. This antibody can be used as a cis-Golgi network marker.

물리적 형태

Solution in 0.01 M phosphate buffered saline, pH 7,.4, containing 15 mM sodium azide.

면책조항

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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관련 제품

제품 번호
설명
가격

Storage Class Code

10 - Combustible liquids

WGK

WGK 3

Flash Point (°F)

Not applicable

Flash Point (°C)

Not applicable


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시험 성적서(COA)

Lot/Batch Number

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이 제품을 이미 가지고 계십니까?

문서 라이브러리에서 최근에 구매한 제품에 대한 문서를 찾아보세요.

문서 라이브러리 방문

dGRASP localization and function in the early exocytic pathway in Drosophila S2 cells
Kondylis V, et al.
Molecular Biology of the Cell, 16, 4061-4072 (2005)
Neuronal Expression and Subcellular Localization of Cholesterol 24-Hydroxylase in the Mouse Brain
Ramirez DMO, et al.
The Journal of Comparative Neurology, 507, 1676-1676 (2008)
Excess centrosomes perturb dynamic endothelial cell repolarization during blood vessel formation
Kushner EJ, et al.
Molecular Biology of the Cell, 27(12), 1911-1920 (2016)
Rab1 interaction with a GM130 effector complex regulates COPII vesicle cis-Golgi tethering
Moyer BD, et al.
Traffic, 2, 268-276 (2001)
Characterization of a cis-Golgi matrix protein, GM130
Nakamura N, et al.
The Journal of Cell Biology, 131, Pt-Pt (1995)

문서

The isolation of subcellular fractions by centrifugation is a commonly used technique and is widely applicable across multiple cell and tissue types. Because organelles differ in their size, shape, and density, centrifugation can be easily employed to separate and purify organelle fractions from gently homogenized samples.

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