RRBP1 Antikörper
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- Target Alle RRBP1 Antikörper anzeigen
- RRBP1 (Ribosome Binding Protein 1 (RRBP1))
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Reaktivität
- Human, Maus, Ratte
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Wirt
- Kaninchen
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Klonalität
- Polyklonal
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Konjugat
- Dieser RRBP1 Antikörper ist unkonjugiert
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Applikation
- Western Blotting (WB), Flow Cytometry (FACS), Immunohistochemistry (Paraffin-embedded Sections) (IHC (p)), Immunocytochemistry (ICC), Immunohistochemistry (Frozen Sections) (IHC (fro))
- Verwendungszweck
- Rabbit IgG polyclonal antibody for RRBP1 detection. Tested with WB, IHC-P, IHC-F, ICC, FCM in Human,Mouse,Rat.
- Sequenz
- EKEKKLTSDL GRAATRLQEL LKTTQEQLAR EKDTVKKLQE QLEKAED
- Kreuzreaktivität (Details)
- No cross reactivity with other proteins.
- Produktmerkmale
- Rabbit IgG polyclonal antibody for RRBP1 detection. Tested with WB, IHC-P, IHC-F, ICC, FCM in Human,Mouse,Rat.
- Aufreinigung
- Immunogen affinity purified.
- Immunogen
- A synthetic peptide corresponding to a sequence of human RRBP1(EKEKKLTSDLGRAATRLQELLKTTQEQLAREKDTVKKLQEQLEKAED).
- Isotyp
- IgG
- Top Product
- Discover our top product RRBP1 Primärantikörper
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- Applikationshinweise
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Application details: Western blot|0.1-0.5 μg/mL Immunohistochemistry(Paraffin-embedded Section)|0.5-1 μg/mL Immunohistochemistry(Frozen Section)|0.5-1 μg/mL Immunocytochemistry|0.5-1 μg/mL Flow Cytometry|1-3 μg/1x106 cells
- Kommentare
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Tested Species: In-house tested species with positive results. By Heat: Boiling the paraffin sections in 10mM citrate buffer, pH6.0, for 20mins is required for the staining of formalin/paraffin sections. Other applications have not been tested. Optimal dilutions should be determined by end users.
- Beschränkungen
- Nur für Forschungszwecke einsetzbar
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- Format
- Lyophilized
- Rekonstitution
- Add 0.2 mL of distilled water will yield a concentration of 500 μg/mL.
- Buffer
- Each vial contains 4 mg Trehalose, 0.9 mg NaCl, 0.2 mg Na2HPO4, 0.05 mg Sodium azide.
- Konservierungsmittel
- Sodium azide
- Vorsichtsmaßnahmen
- This product contains Sodium azide: a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.
- Lagerung
- 4 °C,-20 °C
- Informationen zur Lagerung
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At -20°C for one year. After reconstitution, at 4°C for one month.
It can also be aliquotted and stored frozen at -20 °C for a longer time. Avoid repeated freezing and thawing.
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- Target
- RRBP1 (Ribosome Binding Protein 1 (RRBP1))
- Andere Bezeichnung
- RRBP1 (RRBP1 Produkte)
- Synonyme
- 1700087N07Rik antikoerper, 5730465C04Rik antikoerper, ES/130 antikoerper, mKIAA1398 antikoerper, mRRp0 antikoerper, mRRp1.8 antikoerper, mRRp10 antikoerper, mRRp15a antikoerper, mRRp15b antikoerper, mRRp16.8 antikoerper, mRRp2 antikoerper, mRRp41 antikoerper, mRRp47 antikoerper, mRRp5.4 antikoerper, p180 antikoerper, ES130 antikoerper, RRp antikoerper, hES antikoerper, P180 antikoerper, rrbp1 antikoerper, sb:cb489 antikoerper, wu:fc47a01 antikoerper, ribosome binding protein 1 antikoerper, ribosome binding protein 1 homolog 180kDa (dog) antikoerper, ribosome binding protein 1b antikoerper, Rrbp1 antikoerper, RRBP1 antikoerper, rrbp1b antikoerper
- Hintergrund
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Synonyms: Ribosome-binding protein 1, 180 kDa ribosome receptor homolog, RRp, ES/130-related protein, Ribosome receptor protein, RRBP1, KIAA1398
Background: Ribosome-binding protein 1, also referred to as p180, is a protein that in humans is encoded by the RRBP1 gene. It is mapped to 20p12.1. This gene encodes a ribosome-binding protein of the endoplasmic reticulum (ER) membrane. Studies suggest that this gene plays a role in ER proliferation, secretory pathways and secretory cell differentiation, and mediation of ER-microtubule interactions. Alternative splicing has been observed and protein isoforms are characterized by regions of N-terminal decapeptide and C-terminal heptad repeats. Splicing of the tandem repeats results in variations in ribosome-binding affinity and secretory function. The full-length nature of variants which differ in repeat length has not been determined. Pseudogenes of this gene have been identified on chromosomes 3 and 7, and RRBP1 has been excluded as a candidate gene in the cause of Alagille syndrome, the result of a mutation in a nearby gene on chromosome 20p12.
- Gen-ID
- 6238
- UniProt
- Q9P2E9
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