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当前位置: 首页 > 产品中心 > Goat_resistance > GenWay/绵羊/山羊IgG抗体(FITC)/GWB-74034D/1 mg
商品详细GenWay/绵羊/山羊IgG抗体(FITC)/GWB-74034D/1 mg
GenWay/绵羊/山羊IgG抗体(FITC)/GWB-74034D/1 mg
GenWay/绵羊/山羊IgG抗体(FITC)/GWB-74034D/1 mg
商品编号: GWB-74034D
品牌: genwaybio
市场价: ¥11580.00
美元价: 8685.00
产地: 美国(厂家直采)
公司:
产品分类: 抗山羊
公司分类: Goat_resistance
联系Q Q: 3392242852
电话号码: 4000-520-616
电子邮箱: info@ebiomall.com
商品介绍

Description:

Short Description: DONKEY ANTI SHEEP/GOAT IgGFITC

Additional Information:

Name Sheep/Goat IgG Antibody (FITC)
Related Product Names DONKEY ANTI SHEEP/GOAT IgG: FITC IgGIGHG1
Gene Symbol IGHG3
Gene Family IGH
Gene id 3502
Alias Symbols IgG3, FLJ39988, FLJ40036, FLJ40253, FLJ40587, FLJ40789, FLJ40834, MGC45809, DKFZp686H11213, IGHG3
Description of Target DONKEY ANTI SHEEP/GOAT IgG:FITC
Swissprot ID P01860
Species Reactivity Sheep
Host Donkey
Isotype Polyclonal IgG
Conjugation FITC
Replacement This antibody may replace item sc-34663 from Santa Cruz Biotechnology.
Immunogen Sheep IgG
Homology Sheep
Product Format Purified IgG conjugated to Fluorescein Isothiocyanate Isomer 1 (FITC) - liquid
Specificity IgG
Concentration 1mg/ml
Applications C
Application Info Immunohistology - Frozen:    1/100 - 1/200
Clonality Polyclonal
Format Solution: Phosphate buffered saline, Stabalizer: 0.09%, Sodium Azide. 1%, Bovine Serum Albumin, Form: Purified IgG conjugated to Fluorescein Isothiocyanate Isomer 1 (FITC) - liquid
Stability 18 months from date of despatch.
Reconstitution and Storage Store at +4oC or at -20oC if preferred.
This product should be stored undiluted.
Storage in frost-free freezers is not recommended. This product is photosensitive and should be protected from light.
Avoid repeated freezing and thawing as this may denature the antibody. Should this product contain a precipitate we recommend microcentrifugation before use.
Reactivity Sheep
Storage Store at +4°C or at -20°C if preferred. This product should be stored undiluted. Storage in frost-free freezers is not recommended. This product is photosensitive and should be protected from light. Avoid repeated freezing and thawing as this
Protocol Information Citation: 1: Hallström T, Resman F, Ristovski M, Riesbeck K. Binding of complement regulators to invasive nontypeable Haemophilus influenzae isolates is not increased compared to nasopharyngeal isolates, but serum resistance is linked to disease severity. J Clin Microbiol. 2010 Mar;48(3):921-7. Epub 2010 Jan 20. PubMed PMID: 20089757; PubMed Central PMCID: PMC2832458.
Species: Normal Human Serum(NHS)
Experiment Name: Serum binding assay
Experiment Background: In the present study, the characteristics of invasive nontypeable Haemophilus influenzae (NTHi) infections, including evidence of immune deficiency in the individual patient and the clinical presentation of the septic event, were studied. Teresia et al. correlated these findings with the capacity to bind specific complement regulators and the in vitro serum resistance of the individual isolates.
Experimental Steps: 1. To analyze whether NTHi from different isolation sites bound C4BP or factor H directly from NHS, bacteria were grown overnight in BHI broth. NTHi bacteria (109) were incubated with hiNHS and buffer (100 mM NaCl, 50 mM Tris-HCl, pH 7.4) for 1 h at37°C. 2. To remove unbound proteins, bacteria were washed 5 times with the same buffer. Thereafter, the bacterial pellet was resuspended in 150 µl of 0.1 M glycine-HCl, pH 2.0, in order to elute bound proteins.3. Bacteria without NHS were used as a negative control. After 15 min of incubation at 37°C with shaking, bacteria were centrifuged and the supernatants were subjected to SDS-PAGE (10%).4. To analyze whether NTHi bound vitronectin from NHS, bacteria were grown overnight and incubated with hiNHS and PBS. To removeunbound proteins, NTHi bacteria were washed 5 times with the same buffer.5. Thereafter, the bacterial pellet was resuspended in 50 µl of 0.1% Triton X-100 (Darmstadt, Germany) and protease inhibitors (Complete; Roche, Mannheim, Germany).6. After 30 min of incubation at 4°C, bacteria were centrifuged and the supernatants were subjected to SDS-PAGE (10%).7. Electrophoretic transfer of protein bands from the gel to an Immobilon-P membrane (Millipore, Bedford, MA) was done at 35 V for 2 h. After transfer, the Immobilon-P membrane was blocked in PBS with 0.1% Tween 20 (PBS-Tween) containing 5% milk powder. After several washings, the membrane was incubated with rabbit anti-human C4BP, goat anti-human factor H, or goat anti-human vitronectin pAb, followed by incubation with HRP-conjugated swine anti-rabbit or donkey-anti-goat pAb.8. After incubation and additional washings in PBS-Tween, development was performed with enhanced chemiluminescence (ECL) Western blotting detection reagents (Pierce, Rockford, IL).
Other Reagents Used: NaCl, glucose, gelatin, MgCl2 , CaCl2.
Number Of Protocols: 1
Lead Time Domestic: within 2-3 weeks delivery International: 2-3 weeks
Intended Use Research Use Only
Key Reference 1. Singh, M. et al. (1999) A recombinant measles virus expressing hepatitis B virus surface antigen induces humoral immune responses in genetically modified mice. J. Virol. 73 (6): 4823 - 4828.
2. Tedla, N. et al. (1998) Regulation of T lymphocyte trafficking into lymph nodes during an immune response by the chemokines macrophage inflammatory protein (MIP) - 1 alpha and MIP-1 beta. J. Immunol. 161: 5663 - 5672
3. Turner, J. et al. (2002) in vivo IL-10 production reactivates chronic pulmonary tuberculosis in C57BL/6 mice. J. Immunol. 169: 6343 - 6351.
:: Preservative Stabilisers: 0.09% - Sodium Azide
1% - Bovine Serum Albumin
Antiserum Preparation: Antisera to sheep IgG were raised by repeated immunisation of donkeys with highly purified antigen. Purified IgG was prepared by affinity chromatography.
:: Approx Protein Conc: IgG concentration 1.0 mg/ml
Buffer Solutions: Phosphate buffered saline pH7.2
品牌介绍
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