DNA-binding protein SMUBP-2, ELISA Kit

CATF1; FLJ34220; FLJ41171; HCSA; HMN6; SMARD1; SMUBP2; cardiac transcription factor 1

For Research Use Only. Not for use in diagnostic procedures.

This assay has high sensitivity and excellent specificity for detection of Rat IGHMBP2. No significant cross-reactivity or interference between Rat IGHMBP2 and analogues was observed.

Store at 2-8 degree C.

Select online data sheet information is drawn from bioinformatics databases, occasionally resulting in ambiguous or non-relevant product information. It is the responsibility of the customer to review, verify, and evaluate the information to make sure it matches their requirements before purchasing the kit. Our ELISA Kit assays are dynamic research tools and sometimes they may be updated and improved. If the format of this assay is important to you then please request the current manual or contact our technical support team with a presales inquiry before placing an order. We will confirm the current details of the assay. We cannot guarantee the sample manual posted online is the most current manual.

Small volumes of IGHMBP2 elisa kit vial(s) may occasionally become entrapped in the seal of the product vial during shipment and storage. If necessary, briefly centrifuge the vial on a tabletop centrifuge to dislodge any liquid in the container`s cap. Certain products may require to ship with dry ice and additional dry ice fee may apply.

MBS285094 is a ready-to-use microwell, strip plate ELISA (enzyme-linked immunosorbent assay) Kit for analyzing the presence of the DNA-binding protein SMUBP-2 (IGHMBP2) ELISA Kit target analytes in biological samples. The concentration gradients of the kit standards or positive controls render a theoretical kit detection range in biological research samples containing IGHMBP2. The ELISA analytical biochemical technique of the MBS285094 kit is based on IGHMBP2 antibody-IGHMBP2 antigen interactions (immunosorbency) and an HRP colorimetric detection system to detect IGHMBP2 antigen targets in samples. The ELISA Kit is designed to detect native, not recombinant, IGHMBP2. Appropriate sample types may include undiluted body fluids and/or tissue homogenates, secretions. Quality control assays assessing reproducibility identified the intra-assay CV (%) and inter-assay CV(%).

Principle of the Assay: This assay employs a two-site sandwich ELISA to quantitate IGHMBP2 in samples. An antibody specific for IGHMBP2 has been pre-coated onto a microplate. Standards and samples are pipetted into the wells and anyIGHMBP2 present is bound by the immobilized antibody. After removing any unbound substances, a biotin-conjugated antibody specific for IGHMBP2 is added to the wells. After washing, Streptavidin conjugated Horseradish Peroxidase (HRP) is added to the wells. Following a wash to remove any unbound avidin-enzyme reagent, a substrate solution is added to the wells and color develops in proportion to the amount of IGHMBP2 bound in the initial step. The color development is stopped and the intensity of the color is measured.

108,440 Da

immunoglobulin mu binding protein 2

DNA-binding protein SMUBP-2

DNA-binding protein SMUBP-2

Smbp2; AEP  [Similar Products]

forms a DNA-protein complex with element B [RGD, Feb 2006]

5' to 3' helicase that unwinds RNA and DNA duplices in an ATP-dependent reaction. Acts as a transcription regulator. Required for the transcriptional activation of the flounder liver-type antifreeze protein gene. Exhibits strong binding specificity to the enhancer element B of the flounder antifreeze protein gene intron. Binds to the insulin II gene RIPE3B enhancer region (). May be involved in translation. DNA-binding protein specific to 5'-phosphorylated single-stranded guanine-rich sequence related to the immunoglobulin mu chain switch region. Preferentially binds to the 5'-GGGCT-3' motif. Interacts with tRNA-Tyr ().

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