PA5-19857
antibody from Invitrogen Antibodies
Targeting: CXCR4
CD184, D2S201E, fusin, HM89, HSY3RR, LESTR, NPY3R, NPYR, NPYY3R
Antibody data
- Antibody Data
- Antigen structure
- References [1]
- Comments [0]
- Validations
- Western blot [1]
- Other assay [1]
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Validation data
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- Product number
- PA5-19857 - Provider product page
- Provider
- Invitrogen Antibodies
- Product name
- CXCR4 Polyclonal Antibody
- Antibody type
- Polyclonal
- Antigen
- Synthetic peptide
- Description
- A suggested positive control is Hela cell lysate. PA5-19857 can be used with blocking peptide PEP-0002. The PA5-19857 immunogen is located within amino acids 170-220 of CXCR4. Predicted molecular ~ 40kD. In Western blot applications, this antibody has been observed to detect a band at: 44kD (Post-modification: 2 N-linked glycosylation) Predicted species reactivity based on immunogen sequence: Pig: (100%), Bovine: (86%), Sheep: (86%), Mouse: (73%), Rat: (67%)
- Reactivity
- Human, Mouse, Rat
- Host
- Rabbit
- Isotype
- IgG
- Vial size
- 100 µg
- Concentration
- 1 mg/mL
- Storage
- Maintain refrigerated at 2-8°C for up to 3 months. For long term storage store at -20°C
Submitted references Cigarette smoke promotes HIV infection of primary bronchial epithelium and additively suppresses CFTR function.
Chinnapaiyan S, Dutta R, Bala J, Parira T, Agudelo M, Nair M, Unwalla HJ
Scientific reports 2018 May 22;8(1):7984
Scientific reports 2018 May 22;8(1):7984
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Supportive validation
- Submitted by
- Invitrogen Antibodies (provider)
- Main image
- Experimental details
- Western blot analysis of HeLa total cell lysate using a CD184/CXCR4 polyclonal antibody (Product # PA5-19857) at 1:1000 dilution.
Supportive validation
- Submitted by
- Invitrogen Antibodies (provider)
- Main image
- Experimental details
- Figure 2 CS increases expression of HIV receptors CD4 and CCR5 in NHBE ALI cultures. NHBE ALI cultures were exposed to CS and total protein was extracted. Cells were lysed with RIPA buffer containing protease inhibitor cocktail and protein expression was quantified by Western blot analysis and normalized using beta-actin. CS significantly enhances expression of CD4 (panel a) and CCR5 protein expression (panel b) when compared to air-exposed controls. CS does not increase CXCR4 protein expression (panel c). Western blot images ( a - c ) are representative of NHBE ALI cultures from three independent lungs. Relative density of the detected protein band was measured by using the ImageJ software and the values obtained were averaged. n = 3 lungs (unless stated otherwise). *Significant (p < 0.05).