추천 제품
생물학적 소스
goat
Quality Level
결합
FITC conjugate
항체 형태
affinity isolated antibody
항체 생산 유형
secondary antibodies
클론
polyclonal
양식
buffered aqueous solution
기술
indirect immunofluorescence: 1:40
저장 온도
2-8°C
타겟 번역 후 변형
unmodified
일반 설명
Goat polyclonal anti-Rabbit IgG (whole molecule), F(ab′)2 fragment–FITC antibody binds all rabbit IgGs.
Immunoglobulins (Igs) are glycoprotein antibodies that modulate several immune responses. Rabbit IgGs against target proteins are often used as primary antibodies in various research applications. Thus, secondary anti-rabbit IgGs can be useful tools for the analysis of target proteins
Anti-Rabbit IgG (whole molecule), (F(ab′)2) fragment-FITC is specific for all rabbit immunoglobulins. The use of this product prevents background staining due to the presence of Fc receptors.
Anti-Rabbit IgG (whole molecule), (F(ab′)2) fragment-FITC is specific for all rabbit immunoglobulins. The use of this product prevents background staining due to the presence of Fc receptors.
Rabbit IgG is a plasma B cell derived antibody isotype defined by its heavy chain. IgG is the most abundant antibody isotype found in rabbit serum. IgG crosses the placental barrier, is a complement activator and binds to the Fc-receptors on phagocytic cells. The level of IgG may vary with the status of disease or infection.
Fluorescein isothiocyanate (FITC) is a fluorescein derivative (fluorochrome) used to tag antibodies, including secondary antibodies, for use in fluorescence-based assays and procedures. FITC excites at 495 nm and emits at 521 nm.
Fluorescein isothiocyanate (FITC) is a fluorescein derivative (fluorochrome) used to tag antibodies, including secondary antibodies, for use in fluorescence-based assays and procedures. FITC excites at 495 nm and emits at 521 nm.
면역원
Purified rabbit IgG
애플리케이션
Anti-Rabbit IgG (whole molecule), (F(ab′)2) fragment-FITC is suitable for use in flow cytometry.
Anti-Rabbit IgG (whole molecule), F(ab′)2 fragment–FITC antibody produced in goat has also been used for fluorescence labeling and immunocytochemistry.
Goat polyclonal anti-Rabbit IgG (whole molecule), F(ab′)2 fragment–FITC antibody may be used to detect and quantitate the level of IgG in rabbut serum and biological fluids by fluorescent techniques. It may also be used as a secondary antibody in assays that use rabbit IgG as the primary antibody. F(ab′)2 fragment–FITC antibody is useful when trying to avoid background staining due to the presence of Fc receptors.
물리적 형태
Solution in 0.01 M phosphate buffered saline, pH 7.4, containing 1% bovine serum albumin and 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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Storage Class Code
10 - Combustible liquids
WGK
nwg
Flash Point (°F)
Not applicable
Flash Point (°C)
Not applicable
Edith Terrenoire et al.
Genome biology, 11(11), R110-R110 (2010-11-17)
Immunolabeling of metaphase chromosome spreads can map components of the human epigenome at the single cell level. Previously, there has been no systematic attempt to explore the potential of this approach for epigenomic mapping and thereby to complement approaches based
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Follo MY, et al.
Leukemia, 25(2), 271-271 (2011)
Differentiation of human alveolar epithelial cells in primary culture: morphological characterization and synthesis of caveolin-1 and surfactant protein-C
Fuchs S, et al.
Cell and Tissue Research, 311(1), 31-45 (2003)
Edith Terrenoire et al.
BMC genetics, 16, 44-44 (2015-05-01)
Using metaphase spreads from human lymphoblastoid cell lines, we previously showed how immunofluorescence microscopy could define the distribution of histone modifications across metaphase chromosomes. We showed that different histone modifications gave consistent and clearly defined immunofluorescent banding patterns. However, it
Milka Luna-Nácar et al.
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