IL-1a Antibody

ProSci
Product Code: PSI-XP-5175
Product Group: Primary Antibodies
Supplier: ProSci
CodeSizePrice
PSI-XP-5175-0.1mg0.1mg£524.00
Quantity:
Prices exclude any Taxes / VAT

Overview

Host Type: Rabbit
Antibody Clonality: Polyclonal
Regulatory Status: RUO
Target Species: Mouse
Applications:
  • Enzyme-Linked Immunosorbent Assay (ELISA)
  • Neutralisation
  • Western Blot (WB)
Storage:
IL-1a antibody is stable for at least 2 years from date of receipt at -20˚C. The reconstituted antibody is stable for at least two weeks at 2-8˚C. Frozen aliquots are stable for at least 6 months when stored at -20˚C. Avoid repeated freeze-

Images

1 / 5
To detect mIL-1-alpha by sandwich ELISA (using 100 ul/well antibody solution) a concentration of 0.5 - 2.0 ug/ml of this antibody is required. This antigen affinity purified antibody, in conjunction with ProSci?s Biotinylated Anti-Murine IL-1-alpha (XP-5175Bt) as a detection antibody, allows the detection of at least 0.2 - 0.4 ng/well of recombinant mIL-1-alpha.
2 / 5
To detect mIL-1-alpha by Western Blot analysis this antibody can be used at a concentration of 0.1-0.2 ug/ml. Used in conjunction with compatible secondary reagents the detection limit for recombinant mIL-1-alpha is 1.5-3.0 ng/lane, under either reducing or non-reducing conditions.
3 / 5
To detect mIL-1-alpha by Western Blot analysis this antibody can be used at a concentration of 0.1-0.2 ug/ml. Used in conjunction with compatible secondary reagents the detection limit for recombinant mIL-1-alpha is 1.5-3.0 ng/lane, under either reducing or non-reducing conditions.
4 / 5
This antibody stained colchicine injected mouse brain (including the hippocampal fissure) tissue.  The primary antibody was incubated at 1.0 mg/ml overnight at 4°C.  This was followed by a peroxidase conjugated secondary antibody and then a fluorescein Tyramide Signal Amplification (TSA) reagent.  Optimal concentrations and conditions may vary.
5 / 5
This antibody stained colchicine injected mouse brain (including the hippocampal fissure) tissue.  The primary antibody was incubated at 1.0 mg/ml overnight at 4°C.  This was followed by a peroxidase conjugated secondary antibody and then a fluorescein Tyramide Signal Amplification (TSA) reagent.  Optimal concentrations and conditions may vary.

To detect mIL-1-alpha by sandwich ELISA (using 100 ul/well antibody solution) a concentration of 0.5 - 2.0 ug/ml of this antibody is required. This antigen affinity purified antibody, in conjunction with ProSci?s Biotinylated Anti-Murine IL-1-alpha (XP-5175Bt) as a detection antibody, allows the detection of at least 0.2 - 0.4 ng/well of recombinant mIL-1-alpha.
To detect mIL-1-alpha by Western Blot analysis this antibody can be used at a concentration of 0.1-0.2 ug/ml. Used in conjunction with compatible secondary reagents the detection limit for recombinant mIL-1-alpha is 1.5-3.0 ng/lane, under either reducing or non-reducing conditions.
To detect mIL-1-alpha by Western Blot analysis this antibody can be used at a concentration of 0.1-0.2 ug/ml. Used in conjunction with compatible secondary reagents the detection limit for recombinant mIL-1-alpha is 1.5-3.0 ng/lane, under either reducing or non-reducing conditions.
This antibody stained colchicine injected mouse brain (including the hippocampal fissure) tissue.  The primary antibody was incubated at 1.0 mg/ml overnight at 4°C.  This was followed by a peroxidase conjugated secondary antibody and then a fluorescein Tyramide Signal Amplification (TSA) reagent.  Optimal concentrations and conditions may vary.
This antibody stained colchicine injected mouse brain (including the hippocampal fissure) tissue.  The primary antibody was incubated at 1.0 mg/ml overnight at 4°C.  This was followed by a peroxidase conjugated secondary antibody and then a fluorescein Tyramide Signal Amplification (TSA) reagent.  Optimal concentrations and conditions may vary.

Further Information

Additional Names:
Il-1aInterleukin-1 alphaIL-1 alpha
Application Note:
Neutralization:
To yield one-half maximal inhibition [ND50] of the biological activity of mIL-1 alpha (0.05 ng/mL), a concentration of 0.03 - 0.05 μg/mL of this antibody is required.

ELISA:

To detect mIL-1 alpha by direct ELISA (using 100 μL/well antibody solution) a concentration of at least 0.5 μg/mL of this antibody is required. This antigen affinity purified antibody, in conjunction with compatible secondary reagents, allows the detection of 0.2 - 0.4 ng/well of recombinant mIL-1 alpha.

Sandwich:

To detect mIL-1α by sandwich ELISA (using 100 μL/well antibody solution) a concentration of 0.5 - 2.0 μg/mL of this antibody is required. This antigen affinity purified antibody, in conjunction with our Biotinylated Anti-Murine IL-1α (XP-5175Bt) as a detection antibody, allows the detection of at least 0.2 - 0.4 ng/well of recombinant mIL-1α.

Western Blot:

To detect mIL-1 alpha by Western Blot analysis this antibody can be used at a concentration of 0.1 - 0.2 μg/mL. Used in conjunction with compatible secondary reagents the detection limit for recombinant mIL-1 alpha is 1.5 - 3.0 ng/lane, under either reducing or non-reducing conditions.
Concentration:
batch dependent
Conjugate:
Unconjugated
Immunogen:
Produced from sera of rabbits pre-immunized with highly pure (>98%) recombinant mIL-1-alpha (murine IL-1 alpha).
NCBI Gene ID #:
16175
NCBI Official Name:
interleukin 1 alpha
NCBI Official Symbol:
Il1a
NCBI Organism:
Mus musculus
Physical State:
Lyophilized
Protein Accession #:
P01582
Protein GI Number:
124298
Purification:
Anti-mIL-1 alpha specific antibody was purified by affinity chromatography employing immobilized mIL-1 alpha matrix.
Research Area:
Immunology,Chemokines & Cytokines,Antibody Pairs, Functional Assays
Swissprot #:
P01582
User NOte:
Centrifuge vial prior to opening.