Vergleich

Mouse Anti-Human Bcl-xL

Hersteller GENWAY
Kategorie
Typ Antibody
Specific against Human
Clon 7B2. 5
Applikationen WB, FC, IP, IHC
Menge 0.1 mg
Host Mouse
ArtNr 20-787-276239
eClass 6.1 32160702
eClass 9.0 32160702
Lieferbar
Genway ID:
GWB-383EB6
Isotype:
Mouse IgG3
Clone:
7B2. 5
Immunogen:
Recombinant Bcl-xS
Characterization:
To insure lot-to-lot consistency each batch of product is tested by immunoassay to conform to the characteristics of a standard reference reagent.
Specificity:
Human Bcl-xL (Mr 29 kDa)Apoptosis or programmed cell death is a well-documented phenomenon in many cellular systems. ^1 It plays a key role in tissue and organ development as well as in adult tissues during cell turnover. Apoptosis can be induced by a variety of internal and external stimuli including growth factor deprivation cytokine treatment antigen-receptor engagement cell-cell interactions irradiation and glucocorticoid treatment. ^2 Bcl-2 and one of its homologues Bcl-xL protect cells from apoptosis^3 4 while other homologues of Bcl-2 such as Bax Bad and Bak have been shown to enhance apoptosis. ^5-8 Bcl-xL has been shown to block apoptosis which is induced by a variety of stimuli and under certain conditions offers greater protection against apoptosis than Bcl-2. ^9-13 In contrast Bad and Bax inhibit the protective functions of Bcl-xL and Bcl-2 respectively. Although heterodimerization between Bcl-xL/Bad and Bcl-2/Bax was originally thought to be essential for the differential anti-apoptotic activity of Bcl-xL and Bcl-2 ^5 14 other results suggest that the formation of heterodimers may not be necessary for this death-repressing activity. ^15 16 Mab 7B2. 5 recognizes both human and rodent Bcl-xL. ^17
Immunofluorescent Staining:
Product: Mouse Anti-Human Bcl-xLAmount Used: 2 ug/10^6 cellsMurine FL5 cells (FL5-NEO) and FL5 cells transfected with Bcl-xL expression plasmid (FL5-BCL-XL) were fixed with buffered paraformaldehyde and then permeabilized with saponin. The cells were incubated with mouse anti-human Bcl-xL followed by phycoerythrin-conjugated goat antimouse IgG and then were analyzed by flow cytometry.
Working Dilution:
Flow Cytometry: 3 ug/10^6 cells
Western Blotting:
0. 5 ug/ml
Warning:
Reagents contain sodium azide. Sodium azide is very toxic if ingested or inhaled. Avoid contact with skin eyes or clothing. Wear eye or face protection when handling. If skin or eye contact occurs wash with copious amounts of water. If ingested or inhaled contact a physician immediately. Sodium azide yields toxic hydrazoic acid under acidic conditions. Dilute azide-containing compounds in running water before discarding to avoid accumulation of potentially explosive deposits in lead or copper plumbing.
Function:
Potent inhibitor of cell death. Isoform Bcl-X(L) anti-apoptotic activity is inhibited by association with SIVA isoform 1. Inhibits activation of caspases (By similarity). Appears to regulate cell death by blocking the voltage-dependent anion channnel (VDAC) by binding to it and preventing the release of the caspase activator cytochrome c from the mitochondrial membrane. The Bcl-X(S) isoform promotes apoptosis.
Subunit:
Bcl-X(L) forms homodimers and heterodimers with BAX BAK and BCL2. Heterodimerization with BAX does not seem to be required for anti-apoptotic activity. Also interacts with BAD and BBC3. Isoform Bcl-X(L) binds to Siva isoform 1. Interacts with BCL2L11 (By similarity). Interacts with BECN1 and PGAM5.
Subcellular Location:
Mitochondrion membrane; Single-pass membrane protein (By similarity). Nucleus envelope; Single-pass membrane protein; Cytoplasmic side (By similarity). Note=Mitochondrial membranes and perinuclear envelope (By similarity).
Tissue Specificity:
Bcl-X(S) is expressed at high levels in cells that undergo a high rate of turnover such as developing lymphocytes. In contrast Bcl-X(L) is found in tissues containing long-lived postmitotic cells such as adult brain.
Domain:
The BH4 motif is required for anti-apoptotic activity. The BH1 and BH2 motifs are required for both heterodimerization with other Bcl-2 family members and for repression of cell death.
Ptm:
Proteolytically cleaved by caspases during apoptosis. The cleaved protein lacking the BH4 motif has pro-apoptotic activity.
Similarity:
Belongs to the Bcl-2 family. Cohen J. J. 1991. Adv. Immunol. 50:55. Cohen J. J. and R. C. Duke. 1992. Annu. Rev. Immunol. 10:2676. Nunez G. and M. F. Clarke. 1994. Trends Cell Biol. 4:399. Cory S. 1995. Annu. Rev. Immunol. 13:513. Oltvai. Z. N. C. L. Millman and S. J. Korsmeyer. 1993. Cell 74:609. Farrow S. N. et al. 1995. Nature 374:731. Chittenden T. et al. 1995. Nature 374:733. Kiefer M. C. et al. 1995. Nature 374:736. Boise L. H. M. Gonzalez-Garcia C. E. Postema L. Ding T. Lindstein L. A. Turka X. Mao G. Nunez and C. B. Thompson 1993. Cell 74:597. Gottschalk A. R. L. H. Boise C. B. Thompson and J. Quintans. 1994. Proc. Natl. Acad. Sci. USA 91:7350. Gonzalez-Garcia M. I. Garcia L. Ding S. O\' Shea L. H. Boise C. B. Thompson and G. Nunez. 1995. Proc. Natl. Acad. Sci. USA 92:4304Dole M. G. R. Jasty M. J. Cooper C. B. Thompson G. Nunez and V. P. Castle. 1995. Can. Res. 55:2576. Shimizu S. et al. 1995. Nature 374:811. Yin X. M. Z. N. Oltvai and S. J. Korsmeyer. 1994. Nature 369:321. Cheng E. H. -Y. et al. 1996. Nature 379:554. Gottschalk A. R. L. H. Boise Z. N. Oltvai M. A. Accavitti S. J. Korsmeyer J. Quintans and C. B. Thompson. 1996. Cell Death and Differentiation 3:113. Boise L. H. 1997. Personal communication. L. Haughan. 1997. Personal communication.

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Alle Produkte sind nur für Forschungszwecke bestimmt. Nicht für den menschlichen, tierärztlichen oder therapeutischen Gebrauch.

Menge: 0.1 mg
Lieferbar: In stock
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Lieferung vsl. bis 30.05.2024 

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