推荐产品
生物来源
sheep
质量水平
抗体产品类型
primary antibodies
克隆
polyclonal
表单
liquid
包含
≤0.1% sodium azide as preservative (Anti-p53 and Anti-Sheep IgG only)
种属反应性
human, rat, mouse
制造商/商品名称
Calbiochem®
储存条件
OK to freeze
同位素/亚型
IgG
运输
wet ice
储存温度
−20°C
靶向翻译后修饰
unmodified
基因信息
human ... TP53(7157)
一般描述
Recognizes the ~53 kDa wild-type and mutant p53 protein in A431 and SVT2 cells and breast carcinoma tissue.
Sheep polyclonal antibody supplied as diluted serum. Recognizes the ~53 kDa wild-type or mutant p53 protein. Supplied with normal sheep serum and biotinylated rabbit anti-sheep IgG.
This Anti-p53 (Ab-7) (Pantropic) Sheep pAb is validated for use in Frozen Sections, Immunoblotting, ICC, Paraffin Sections, IP for the detection of p53 (Ab-7) (Pantropic).
免疫原
Human
recombinant, human p53 protein
应用
Frozen Sections (1:500)
Immunoblotting (1:2500)
Immunocytochemistry (1:500)
Paraffin Sections (1:500, pepsin or heat pre-treatment required)
Immunoprecipitation (chromatin, see application references)
组分
Anti-p53 antisera, normal sheep serum, and biotinylated rabbit anti-sheep IgG
警告
Toxicity: Standard Handling (A)
外形
200 µl diluted (1:4) anti-p53 sheep serum, 500 µl undiluted normal sheep serum, and 100 µl biotinylated rabbit anti-sheep IgG.
分析说明
Positive Control
A431 or SVT2 cells or breast carcinoma tissue
A431 or SVT2 cells or breast carcinoma tissue
其他说明
El-Deiry, W.S., et al. 1994. Cancer Res.54, 1169.
Greenblatt, M.S., et al. 1994. Cancer Res. 54, 4855.
Barak, Y., et al. 1993. EMBO J.12, 461.
Kastan, M.B., et al. 1992. Cell71, 587.
Kuerbitz, S.J. 1992. Proc. Natl. Acad. Sci. USA 89, 7491.
Lane, D.P. 1992. Nature358, 15.
Kastan, M.B., et al. 1991. Cancer Res.51, 6304.
Greenblatt, M.S., et al. 1994. Cancer Res. 54, 4855.
Barak, Y., et al. 1993. EMBO J.12, 461.
Kastan, M.B., et al. 1992. Cell71, 587.
Kuerbitz, S.J. 1992. Proc. Natl. Acad. Sci. USA 89, 7491.
Lane, D.P. 1992. Nature358, 15.
Kastan, M.B., et al. 1991. Cancer Res.51, 6304.
Recommended dilutions for the biotinylated rabbit anti-sheep secondary are 1:25,000-1:200,000 for immunoblotting and 1:10,000 for immunocytochemistry and paraffin sections. For immunoblotting, do not add normal serum, non-fat dried milk, culture medium or other potential sources of biotin to the working solutions (i.e. block with 2-5% fatty acid free BSA). Use streptavidin-horseradish peroxidase (Cat. No. OR03L) or streptavidin-alkaline phosphatase (Cat. No. OR04L) at 10 ng/ml to attach an enzyme to the biotinylated secondary antibody, then visualize using standard colorimetric or chemiluminescent reagents. To maximize sensitivity of immunoblots, preconcentrate samples by immunoprecipitation with Cat. No. OP03, OP09, or OP43, then immunoblot using Cat. No. PC35 and chemiluminescent detection. Antibodies should be titrated for optimal results in individual systems.
法律信息
CALBIOCHEM is a registered trademark of Merck KGaA, Darmstadt, Germany
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储存分类代码
10 - Combustible liquids
Joshua D Dowell et al.
Biochimica et biophysica acta, 1773(3), 358-366 (2007-01-19)
p193/CUL7 is an E3 ubiquitin ligase initially identified as an SV40 Large T Antigen binding protein. Expression of a dominant interfering variant of mouse p193/CUL7 (designated 1152stop) conferred resistance to MG132- and etoposide-induced apoptosis in U2OS cells. Immune precipitation/Western analyses
A Li et al.
Biology of reproduction, 76(3), 362-367 (2006-11-10)
The expression of TRP53 in blastocysts that had been cultured from the zygote stage in vitro for 90 h was compared with that in blastocysts collected from the uterus in C57BL6 (B6) and in F1 hybrid (B6CBF1) strain mice. In
Glen C Ulett et al.
Journal of immunology (Baltimore, Md. : 1950), 175(4), 2555-2562 (2005-08-06)
Apoptosis of murine and human macrophages induced by group B Streptococcus agalactiae (GBS) is likely an important virulence mechanism that is used by the bacteria to suppress the host immune response and to persist at sites of infection. The mechanisms
Vashe Chandrakanthan et al.
Reproductive biology and endocrinology : RB&E, 5, 39-39 (2007-10-18)
In a mouse model, in vitro fertilization or extended embryo culture leads to the increased expression of TRP53 in susceptible embryos. Ablation of the TRP53 gene improved embryo viability indicating that increased expression of TRP53 is a cause of the
Tinke L Vormer et al.
Molecular and cellular biology, 28(24), 7263-7273 (2008-10-22)
Mouse embryonic fibroblasts (MEFs) deficient for pocket proteins (i.e., pRB/p107-, pRB/p130-, or pRB/p107/p130-deficient MEFs) have lost proper G(1) control and are refractory to Ras(V12)-induced senescence. However, pocket protein-deficient MEFs expressing Ras(V12) were unable to exhibit anchorage-independent growth or to form
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