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Anti-beta 2 Microglobulin antibody [B2M-01]
See all beta 2 Microglobulin products (28) ...
Mouse monoclonal [B2M-01] to beta 2 Microglobulin
This antibody reacts with beta-2-microglobulin, associated with cell-surface MHC Class I molecules and other membrane antigens as well as with soluble forms of beta-2-microglobulin. The antibody detected beta-2-microglobulin in U-937 and RAJI cell lines in WB in non reducing conditions however failed to detect a band in JEG-3 and A431 cell lysates. All lysates gave a signal in direct ELISA.
ELISA, Flow Cyt, IP, RIA, WBmore details
Reacts with
Human
Does not react with
Mouse, Rabbit, Chicken, Cow, Dog, Pig
Full length native protein (purified) (Human).
U-937 and RAJI cell lysates
Liquid
Store at +4°C short term (1-2 weeks). Aliquot and store at -20°C or -80°C. Avoid repeated freeze / thaw cycles.
Preservative: 15mM Sodium Azide
Constituents: PBS, pH 7.4
Concentration information loading...
>95% by SDS-PAGE
Purified from ascites using precipitation methods and DEAE-chromatography.
Monoclonal
B2M-01
IgG2a
Cardiovascular >> Blood >> Blood Cell Antigens >> WBC Antigens >> HLA
Cancer >> Tumor biomarkers >> Globulins
Cardiovascular >> Blood >> Serum Proteins
Western blot - beta 2 Microglobulin antibody [B2M-01] (ab759)
(enlarge)
Our Abpromise guarantee covers the use of ab759 in the following tested applications.
The application notes include recommended starting dilutions; optimal dilutions/concentrations should be determined by the end user.
ELISA: Use at an assay dependent dilution.
Flow Cyt: Use at an assay dependent dilution.
IP: Use at an assay dependent dilution.
RIA: Use at an assay dependent dilution. (Dissociation constant of the antibody-soluble b2-microglobulin is 1.5 x 10-8 mol/l as determined by competitive RIA.)
WB: Use a concentration of 2 µg/ml Use under non reducing condition. Detects a band of approximately 13 kDa (predicted molecular weight: 13 kDa).(Use under non reducing conditions. Incubate overnight. Block with 5%milk for 2hrs. )
Component of the class I major histocompatibility complex (MHC). Involved in the presentation of peptide antigens to the immune system.
Defects in B2M are the cause of hypercatabolic hypoproteinemia (HYCATHYP) [MIM:241600]. Affected individuals show marked reduction in serum concentrations of immunoglobulin and albumin, probably due to rapid degradation.
Note=Beta-2-microglobulin may adopt the fibrillar configuration of amyloid in certain pathologic states. The capacity to assemble into amyloid fibrils is concentration dependent. Persistently high beta(2)-microglobulin serum levels lead to amyloidosis in patients on long-term hemodialysis.
Belongs to the beta-2-microglobulin family.
Contains 1 Ig-like C1-type (immunoglobulin-like) domain.
Glycation of Ile-21 is observed in long-term hemodialysis patients.
Secreted. Detected in serum and urine.
Target information above from: UniProt accessionP61769
The UniProt Consortium
The Universal Protein Resource (UniProt) in 2010
Nucleic Acids Res. 38:D142-D148 (2010).
Western blot - beta 2 Microglobulin antibody [B2M-01] (ab759)
![Western blot - beta 2 Microglobulin antibody [B2M-01] (ab759)](/ps/datasheet/Images/0/ab759/ab759_1.jpg)
All lanes : Anti-beta 2 Microglobulin antibody [B2M-01] (ab759) at 2 µg/ml
Lane 1 : JEG-3 cell lysate
Lane 2 : A-431 cell lysate
Lane 3 : U-937 cell lysate
Lane 4 : Raji cell lysate
developed using the ECL technique
Performed under non-reducing conditions.
Predicted band size : 13 kDa
Lysates were separated on 15% SDS–PAGE gel and electrotransferred to a PVDF membrane. The membrane was blocked in PBS/Tween buffer containing 5% non fat dry milk for 2 hours and probed with ab759 at 4°C overnight.
This product has been referenced in:
See all 8 publications for this product
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![Western blot - beta 2 Microglobulin antibody [B2M-01] (ab759)](/ps/datasheet/Images/0/ab759/ab759_1.jpg)
All lanes : Anti-beta 2 Microglobulin antibody [B2M-01] (ab759) at 2 µg/ml
Lane 1 : JEG-3 cell lysate
Lane 2 : A-431 cell lysate
Lane 3 : U-937 cell lysate
Lane 4 : Raji cell lysate
developed using the ECL technique
Performed under non-reducing conditions.
Predicted band size : 13 kDa
Lysates were separated on 15% SDS–PAGE gel and electrotransferred to a PVDF membrane. The membrane was blocked in PBS/Tween buffer containing 5% non fat dry milk for 2 hours and probed with ab759 at 4°C overnight.
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