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BD Pharmingen™ Human Lineage Cocktail 4 (lin 4) (CD2, CD3, CD4, CD7, CD8, CD10, CD11b, CD14, CD19, CD20, CD56, CD235a)
Lineage cocktail 4 staining on enriched human cord blood: Frozen human cord blood mononuclear cells were thawed then enriched using the Human Lineage Cell Depletion Set (Cat No. 560030). The enriched human cord blood was then stained with the human lineage cocktail 4, APC CD34 (Cat. No 340667), BD Horizon™ BV421 CD38 (Cat. No 562444), APC-H7 CD45RA (Cat. No. 560674), BD Horizon™ BV605 CD90 (Cat. No. 562685) and the viability dye 7-AAD (Cat. No.559925). Prospective hematopoietic stem cells (HSCs) were identified by first selecting cells based on the scatter profile (left plot), then the Lineage negative and viable cells (center left plot), then the CD34+CD38- cells (center right plot) and then the CD90+CD45RA- cells (right plot). Flow cytometry was performed on a BD LSRFortessa™ flow cytometry system.
Lineage cocktail 4 staining on enriched human cord blood: Frozen human cord blood mononuclear cells were thawed then enriched using the Human Lineage Cell Depletion Set (Cat No. 560030). The enriched human cord blood was then stained with the human lineage cocktail 4, APC CD34 (Cat. No 340667), BD Horizon™ BV421 CD38 (Cat. No 562444), APC-H7 CD45RA (Cat. No. 560674), BD Horizon™ BV605 CD90 (Cat. No. 562685) and the viability dye 7-AAD (Cat. No.559925). Prospective hematopoietic stem cells (HSCs) were identified by first selecting cells based on the scatter profile (left plot), then the Lineage negative and viable cells (center left plot), then the CD34+CD38- cells (center right plot) and then the CD90+CD45RA- cells (right plot). Flow cytometry was performed on a BD LSRFortessa™ flow cytometry system.
Lineage cocktail 4 staining on enriched human cord blood: Frozen human cord blood mononuclear cells were thawed then enriched using the Human Lineage Cell Depletion Set (Cat No. 560030). The enriched human cord blood was then stained with the human lineage cocktail 4, APC CD34 (Cat. No 340667), BD Horizon™ BV421 CD38 (Cat. No 562444), APC-H7 CD45RA (Cat. No. 560674), BD Horizon™ BV605 CD90 (Cat. No. 562685) and the viability dye 7-AAD (Cat. No.559925). Prospective hematopoietic stem cells (HSCs) were identified by first selecting cells based on the scatter profile (left plot), then the Lineage negative and viable cells (center left plot), then the CD34+CD38- cells (center right plot) and then the CD90+CD45RA- cells (right plot). Flow cytometry was performed on a BD LSRFortessa™ flow cytometry system.
Regulatory Statusの凡例
Becton, Dickinson and Companyの書面による明示的な許諾を得た使用以外での製品の使用は固く禁じられています。
Product Details
説明
The FITC Human Lineage Cocktail 4 has been designed to react with cells from the major hematopoietic lineages, such as T lymphocytes, B lymphocytes, monocytes/macrophages, NK cells, erythrocytes, and granulocytes. This pre-diluted cocktail of twelve FITC-conjugated antibodies is designed to label lineage marker-positive cells for exclusion to facilitate the flow cytometric identification of lineage marker-negative hematopoietic stem cells in human cord blood and bone marrow. Components include clone RPA-2.10, which recognizes CD2; HIT3a, which recognizes CD3; RPA-T4, which recognizes CD4; M-T701, which recognizes CD7 ; HIT8a, which recognizes CD8; HI10a, which recognizes CD10; ICRF44, which recognizes CD11b; M5E2, which recognizes CD14; SJ25-C1, which recognizes CD19; 2H7, which recognizes CD20; B159, which recognizes CD56 and GA-R2 (HIR2), which recognizes CD235a. Additional fluorochrome-labeled reagents may be combined with the FITC Human Lineage Cocktail 4, such as CD34, CD38, CD90 and CD45RA conjugates, to characterize hematopoietic stem cell populations from cord blood or bone marrow.
調製と保管
製品通知
- This reagent has been pre-diluted for use at the recommended Volume per Test. We typically use 1 × 10^6 cells in a 100-µl experimental sample (a test).
- Source of all serum proteins is from USDA inspected abattoirs located in the United States.
- Caution: Sodium azide yields highly toxic hydrazoic acid under acidic conditions. Dilute azide compounds in running water before discarding to avoid accumulation of potentially explosive deposits in plumbing.
- For fluorochrome spectra and suitable instrument settings, please refer to our Multicolor Flow Cytometry web page at www.bdbiosciences.com/colors.
- Please refer to www.bdbiosciences.com/us/s/resources for technical protocols.
コンパニオン製品
Please refer to Support Documents for Quality Certificates
Global - Refer to manufacturer's instructions for use and related User Manuals and Technical data sheets before using this products as described
Comparisons, where applicable, are made against older BD Technology, manual methods or are general performance claims. Comparisons are not made against non-BD technologies, unless otherwise noted.
For Research Use Only. Not for use in diagnostic or therapeutic procedures.