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iFluor™ 647 Conjugated Ki67 Recombinant Rabbit Monoclonal Antibody [SR00-02]

Usd: 429

Specification

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Catalog# HA720163F

iFluor™ 647 Conjugated Ki67 Recombinant Rabbit Monoclonal Antibody [SR00-02]

Application

  • IF-Cell

  • IF-Tissue

  • FC

  • IHC-Fr

Reactivity

  • Human

  • Mouse

  • Rat

Conjugation

  • iFluor™ 647

This product has been cited in peer reviewed publications, see list HERE

Overview

Product Name

iFluor™ 647 Conjugated Ki67 Recombinant Rabbit Monoclonal Antibody [SR00-02]

Antibody Type

Recombinant Rabbit monoclonal Antibody

Immunogen

Synthetic peptide within human Ki67 aa 1,040-1,080.

Species Reactivity

Human, Mouse, Rat

Validated Applications

IF-Cell, IF-Tissue, FC, IHC-Fr

Target Molecular Weight

Predicted band size: 359 kDa

Positive Control

A431, Jurkat cells, human colon carcinoma tissue, mouse small intestine tissue, rat brain tissue, MOLT-4.

Conjugation

iFluor™ 647

Clone Number

SR00-02

RRID

AB_3072100

Reactivity Data

Tested Tested Tested
Verified (internally validated)
Published Tested
Reported in literature (not internally validated)
Predicted Tested
Predicted reactive (based on sequence homology)
Not recommended Tested
Not recommended (failed internal validation)
IHC-Fr FC IF-Cell IF-Tissue
human
 
Tested Tested
Tested Tested
Tested Tested
mouse
Tested Tested
 
 
 
rat
Tested Tested
 
 
 

Product Features

Form

Liquid

Concentration

1 mg/mL.(The concentration of this product may be batch-dependent)

Storage Instructions

Shipped at 4℃. Store at +4℃ short term (1-2 weeks). It is recommended to aliquot into single-use upon delivery. Store at -20℃ long term.

Storage Buffer

Preservative: 0.02% Sodium azide Constituents: 30% Glycerol, 1% BSA, 68.98% PBS

Isotype

IgG

Purification Method

Protein A affinity purified.

Application Dilution

  • IF-Cell

  • 1:250

  • IF-Tissue

  • 1:100

  • FC

  • 1:1,000

  • IHC-Fr

  • 1:500

Target

Function

The Ki-67 protein is a nuclear protein doublet, 345-395 kDa, playing a pivotal role in maintaining cell proliferation. Ki-67 is present in all non-G0 phases of the cell cycle. Beginning in the mid G1, the level increases through S and G2 to reach a peak in M. In the end of M, is is rapidly catabolized. The Ki-67 labelling index (LI), i.e., the percentage of cells in a tissue staining for Ki-67, indicates the growth fraction. For many tumours, the rate of cell proliferation as assessed by Ki-67 immunoreactivity correlates with tumour grade and clinical course. In Non-Hodgkin lymphoma a labelling index of less than 20% is seen in low grade lymphomas, greater than 20% is associated with high grade lymphomas. Low grade lymphomas with a labelling index in excess of 5% have a worse prognosis than those with an index of less than 5%. In Burkitt and Burkitt-like lymphoma, nearly 100% of the nuclei are stained. This can be used as a diagnostic criterion. In gliomas the indices ranges from 0% to 5% for low grade astrocytomas while anaplastic astrocytomas and glioblastomas most frequently show an index above 10%. In soft tissue sarcomas Ki-67 index is positively correlated with mitotic count, cellularity and histological grade. In some benign tumours, like meningioma, a high LI is associated with a high recurrence rate. In dysplasia in Barrett's oesophagus and in granulosa cell tumours and ovarian serous tumours, Ki-67 LI is associated with progression. In the former, reproducibility of dysplasia grading is improved when Ki67 is included. In breast cancer, the proliferative index measured by Ki67 immunoreactivity has both prognostic and predictive value.

Background References

1. Cuylen S. et al. Ki-67 acts as a biological surfactant to disperse mitotic chromosomes. Nature 535:308-312(2016).

2. Booth D.G. et al. Ki-67 is a PP1-interacting protein that organises the mitotic chromosome periphery. Elife 3:E01641-E01641(2014).

Subcellular Location

Nucleus, Chromosome.

UNIPROT

SwissProt: P46013 Human

SwissProt: E9PVX6 Mouse

Entrez Gene: 246042 Rat

Synonyms

Antigen identified by monoclonal antibody Ki 67 antibody

Antigen identified by monoclonal antibody Ki-67 antibody

Antigen KI-67 antibody

Antigen KI67 antibody

Antigen Ki67 antibody

KI67_HUMAN antibody

KIA antibody

Marker of proliferation Ki-67 antibody

MIB 1 antibody

MIB antibody

Expand

Images

  • Immunocytochemistry analysis of A431 cells labeling Ki67 with Rabbit anti-Ki67 antibody (<a href="/products/HA720163F" style="font-weight: bold;text-decoration: underline;">HA720163F</a>) at 1/250 dilution.<br /><br />Cells were fixed in 4% paraformaldehyde for 20 minutes at room temperature, permeabilized with 0.1% Triton X-100 in PBS for 5 minutes at room temperature, then blocked with 1% BSA in 10% negative goat serum for 1 hour at room temperature. Cells were then incubated with Rabbit anti-Ki67 antibody (<a href="/products/HA720163F" style="font-weight: bold;text-decoration: underline;">HA720163F</a>, red) at 1/250 dilution in 1% BSA in PBST overnight at 4 ℃. Nuclear DNA was labelled in blue with DAPI.<br /><br />Beta tubulin (<a href="/products/M1305-2" style="font-weight: bold;text-decoration: underline;">M1305-2</a>, green) was stained at 1/100 dilution overnight at +4℃. Goat Anti-Mouse IgG H&L (iFluor&trade; 488, <a href="/products/HA1125" style="font-weight: bold;text-decoration: underline;">HA1125</a>) was used as the secondary antibody at 1/1,000 dilution.

    Immunocytochemistry analysis of A431 cells labeling Ki67 with Rabbit anti-Ki67 antibody (HA720163F) at 1/250 dilution.

    Cells were fixed in 4% paraformaldehyde for 20 minutes at room temperature, permeabilized with 0.1% Triton X-100 in PBS for 5 minutes at room temperature, then blocked with 1% BSA in 10% negative goat serum for 1 hour at room temperature. Cells were then incubated with Rabbit anti-Ki67 antibody (HA720163F, red) at 1/250 dilution in 1% BSA in PBST overnight at 4 ℃. Nuclear DNA was labelled in blue with DAPI.

    Beta tubulin (M1305-2, green) was stained at 1/100 dilution overnight at +4℃. Goat Anti-Mouse IgG H&L (iFluor™ 488, HA1125) was used as the secondary antibody at 1/1,000 dilution.

  • Immunofluorescence analysis of paraffin-embedded Jurkat cells labeling Ki67 with Rabbit anti-Ki67 antibody (<a href="/products/HA720163F" style="font-weight: bold;text-decoration: underline;">HA720163F</a>) at 1/100 dilution.<br /><br />The section was pre-treated using heat mediated antigen retrieval with Tris-EDTA buffer (pH 9.0) for 20 minutes. The tissues were blocked in 10% negative goat serum for 1 hour at room temperature, washed with PBS, and then probed with the primary antibody (<a href="/products/HA720163F" style="font-weight: bold;text-decoration: underline;">HA720163F</a>, red) at 1/100 dilution overnight at 4 ℃, washed with PBS.

    Immunofluorescence analysis of paraffin-embedded Jurkat cells labeling Ki67 with Rabbit anti-Ki67 antibody (HA720163F) at 1/100 dilution.

    The section was pre-treated using heat mediated antigen retrieval with Tris-EDTA buffer (pH 9.0) for 20 minutes. The tissues were blocked in 10% negative goat serum for 1 hour at room temperature, washed with PBS, and then probed with the primary antibody (HA720163F, red) at 1/100 dilution overnight at 4 ℃, washed with PBS.

  • Immunofluorescence analysis of paraffin-embedded human colon carcinoma tissue labeling Ki67 (<a href="/products/HA720163F" style="font-weight: bold;text-decoration: underline;">HA720163F</a>).<br /><br />The section was pre-treated using heat mediated antigen retrieval with sodium citrate buffer (pH 6.0) (high pressure) for 2 minutes. The tissues were blocked in 10% negative goat serum for 1 hour at room temperature, washed with PBS. And then probed with the primary antibody Ki67 (<a href="/products/HA720163F" style="font-weight: bold;text-decoration: underline;">HA720163F</a>, red) at 1/100 dilution overnight at 4 ℃, washed with PBS. DAPI was used as nuclear counterstain.

    Immunofluorescence analysis of paraffin-embedded human colon carcinoma tissue labeling Ki67 (HA720163F).

    The section was pre-treated using heat mediated antigen retrieval with sodium citrate buffer (pH 6.0) (high pressure) for 2 minutes. The tissues were blocked in 10% negative goat serum for 1 hour at room temperature, washed with PBS. And then probed with the primary antibody Ki67 (HA720163F, red) at 1/100 dilution overnight at 4 ℃, washed with PBS. DAPI was used as nuclear counterstain.

  • Application: IHC-Fr<br /><br />Species: Mouse<br /><br />Site: small intestine<br /><br />Sample: Frozen section<br /><br />Antibody concentration: 1/500<br /><br />Antigen retrieval: Not required

    Application: IHC-Fr

    Species: Mouse

    Site: small intestine

    Sample: Frozen section

    Antibody concentration: 1/500

    Antigen retrieval: Not required

  • Application: IHC-Fr<br /><br />Species: Rat<br /><br />Site: brain<br /><br />Sample: Frozen section<br /><br />Antibody concentration: 1/500<br /><br />Antigen retrieval: Not required

    Application: IHC-Fr

    Species: Rat

    Site: brain

    Sample: Frozen section

    Antibody concentration: 1/500

    Antigen retrieval: Not required

  • Flow cytometric analysis of MOLT-4 cells labeling Ki67.<br /><br />Cells were washed twice in 1x PBS and fixed in 70% ethanol at 4℃ overnight. Then incubated for 1 hour at +4℃ with Ki67 (<a href="/products/HA720163F" style="font-weight: bold;text-decoration: underline;">HA720163F</a>, red, 1/1,000) and Rabbit IgG Isotype Control (iFluor&trade; 647, green, 1/1,000). Unlabelled sample was used as a control (cells without incubation with primary antibody; black).

    Flow cytometric analysis of MOLT-4 cells labeling Ki67.

    Cells were washed twice in 1x PBS and fixed in 70% ethanol at 4℃ overnight. Then incubated for 1 hour at +4℃ with Ki67 (HA720163F, red, 1/1,000) and Rabbit IgG Isotype Control (iFluor™ 647, green, 1/1,000). Unlabelled sample was used as a control (cells without incubation with primary antibody; black).

Citation

Please note: All products are "FOR RESEARCH USE ONLY AND ARE NOT INTENDED FOR DIAGNOSTIC OR THERAPEUTIC USE"

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