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33905
Keratin 5 (E2T4B) XP® Rabbit mAb (Alexa Fluor® 488 Conjugate)
Antibody Conjugates
Monoclonal Antibody
R
Recombinant

Keratin 5 (E2T4B) XP® Rabbit mAb (Alexa Fluor® 488 Conjugate) #33905

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  1. IHC
  2. IF
Immunohistochemical analysis of paraffin-embedded human urothelial carcinoma using Keratin 5 (E2T4B) XP® Rabbit mAb (Alexa Fluor® 488 Conjugate) (green) and DAPI #4083 (blue).
Immunohistochemical analysis of paraffin-embedded normal human thymus using Keratin 5 (E2T4B) XP® Rabbit mAb (Alexa Fluor® 488 Conjugate) (green) and DAPI #4083 (blue).
Confocal immunofluorescent analysis of fixed frozen mouse skin labeled with Keratin 5 (E2T4B) XP® Rabbit mAb (Alexa Fluor® 488 Conjugate) (green), Vimentin (D21H3) XP® Rabbit mAb (Alexa Fluor® 555 Conjugate) #9855 (red), and DAPI #4083 (blue).
Confocal immunofluorescent analysis of BxPC-3 cells (left, positive) and PANC-1 cells (right, negative) using Keratin 5 (E2T4B) XP® Rabbit mAb (Alexa Fluor® 488 Conjugate) (green), DyLight 650 Phalloidin #12956 (red), and DAPI #4083 (blue).
To Purchase # 33905
Cat. # Size Qty. Price
33905S
100 µl  (50 tests)

Supporting Data

REACTIVITY H M
SENSITIVITY Endogenous
MW (kDa)
Source/Isotype Rabbit IgG

Application Key:

  • WB-Western Blot
  • IP-Immunoprecipitation
  • IHC-Immunohistochemistry
  • ChIP-Chromatin Immunoprecipitation
  • C&R-CUT&RUN
  • C&T-CUT&Tag
  • DB-Dot Blot
  • eCLIP-eCLIP
  • IF-Immunofluorescence
  • F-Flow Cytometry

Species Cross-Reactivity Key:

  • H-Human
  • M-Mouse
  • R-Rat
  • Hm-Hamster
  • Mk-Monkey
  • Vir-Virus
  • Mi-Mink
  • C-Chicken
  • Dm-D. melanogaster
  • X-Xenopus
  • Z-Zebrafish
  • B-Bovine
  • Dg-Dog
  • Pg-Pig
  • Sc-S. cerevisiae
  • Ce-C. elegans
  • Hr-Horse
  • GP-Guinea Pig
  • Rab-Rabbit
  • All-All Species Expected

Product Description

This Cell Signaling Technology® antibody is conjugated to Alexa Fluor® 488 fluorescent dye under optimal conditions. This antibody conjugate is expected to exhibit the same species cross-reactivity as the unconjugated Keratin 5 (E2T4B) XP® Rabbit mAb #71536.

Product Usage Information

Application Dilution
Immunohistochemistry (Paraffin) 1:100 - 1:400
Immunofluorescence (Frozen) 1:800 - 1:1600
Immunofluorescence (Immunocytochemistry) 1:400 - 1:800

Storage

Supplied in PBS (pH 7.2), less than 0.1% sodium azide, and 2 mg/mL BSA. Store at 4°C. Do not aliquot the antibody. Protect from light. Do not freeze.

Protocol

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Immunohistochemistry (Paraffin)

A. Solutions and Reagents

NOTE: Prepare solutions with reverse osmosis deionized (RODI) or equivalent grade water.

  1. Xylene.
  2. Ethanol, anhydrous denatured, histological grade (100% and 95%).
  3. Deionized water (dH2O).
  4. Wash Buffer:
    1. 1X Tris Buffered Saline with Tween® 20 (TBST): To prepare 1 L 1X TBST, add 100 ml 10X Tris Buffered Saline with Tween® 20 (TBST)(#9997) to 900 ml dH20, mix.
    2. 1X Phosphate Buffered Saline (PBS): To prepare 1L 1X PBS, add 100 mL 10X Wash Buffer, Phosphate Buffered Saline(#12528) to 900 ml dH20, mix.
  5. 1X Phosphate Buffered Saline with Tween® 20 Antibody Diluent: To prepare 5 mL of 1X PBST, dilute 250 µl of Phosphate Buffered Saline with Tween® 20 (PBST-20X) (#9809) with 5 ml dH20.
  6. 1X EDTA Unmasking Solution: To prepare 250 mL of 1X EDTA unmasking solution, dilute 25 ml of SignalStain® EDTA Unmasking Solution (10X) (#14747) with 225 ml dH20.
  7. Blocking Solution: 1X TBST/5% Normal Goat Serum or 1X Animal-Free Blocking Solution.
    1. TBST/5% Normal Goat Serum: to 5 ml 1X TBST, add 250 µl Normal Goat Serum (#5425).
    2. 1X Animal-Free Blocking Solution: to 4 mL of dH2O, add 1 ml of Animal-Free Blocking Solution (5X) (#15019).
  8. Prolong® Gold AntiFade Reagent(#9071), Prolong® Gold AntiFade Reagent with DAPI(#8961).
  9. (optional) TrueBlack® Lipofuscin Autofluorescence Quencher (#92401).

B. Deparaffinization/Rehydration

NOTE: Do not allow slides to dry at any time during this procedure.

  1. Deparaffinize/hydrate sections:
    1. Incubate sections in three washes of xylene for 5 minutes each.
    2. Incubate sections in two washes of 100% ethanol for 10 minutes each.
    3. Incubate sections in two washes of 95% ethanol for 10 minutes each.
  2. Wash sections twice in dH2O for 5 minutes each.

C. Antigen Unmasking

  1. Heat slides submersed in 1X EDTA unmasking solution in a microwave until boiling is initiated; follow with 15 min at sub-boiling temperature (95°C-98°C). No cooling is necessary.

D. Staining

  1. Wash sections in dH2O three times for 5 minutes each.
  2. Incubate sections in 1X TBST for 5 min.
  3. Block each section with 100-400 µl of preferred blocking solution for 1 hour at room temperature.
  4. Remove blocking solution and add 100-400 µl primary antibody diluted in 1X Phosphate Buffered Saline with Tween® 20 Antibody Diluent (#9809) to each section.
  5. Incubate overnight at 4°C.
  6. Rinse three times in 1X PBS for 5 min each protected from light.
    NOTE: See below for optional TrueBlack® Lipofuscin Autofluorescence Quencher protocol.
  7. Coverslip slides with Prolong® Gold Antifade Reagent or Prolong® Gold Antifade Reagent with DAPI.
  8. For best results, allow mountant to cure overnight at room temperature. For long-term storage, store slides flat at 4°C protected from light.

TrueBlack® Lipofuscin Autofluorescence Quencher protocol

Following Section D Step 6:

IMPORTANT: TrueBlack® Lipofuscin Autofluorescence Quencher is not compatible with detergent. Any steps involving detergent must be done before applying TrueBlack® Lipofuscin Autofluorescence Quencher.

  1. Prepare TrueBlack® Lipofuscin Autofluorescence Quencher solution by diluting 1:20 in 70% ethanol. Vortex to mix.
    NOTE: Quenching solution should be made fresh prior to use and discarded if precipitate is visible. We recommend heating the vial of stock solution of TrueBlack® Lipofuscin Autofluorescence Quencher, 20X in DMF to 70°C prior to dilution in order to avoid precipitate formation.
  2. Immediately cover tissue sections with 100 µL - 200 µL of quenching solution for 30 seconds at room temperature.
    IMPORTANT: Do not allow sections to dry out. Sections may tolerate longer incubations (up to 3 minutes) so long as they remain hydrated.
  3. Tap slides on an absorbent towel to collect excess TrueBlack® Lipofuscin Autofluorescence Quencher before transferring to 1X PBS.
  4. Rinse three times in 1X PBS for 5 min each.
  5. Proceed with counterstaining/mounting.

Protocol Id: 3244

Immunofluorescence (Frozen Tissue), BSA-free Protocol for Directly Conjugated Antibodies

A. Solutions and Reagents

NOTE: Prepare solutions with reverse osmosis deionized (RODI) or equivalently purified water.

  1. 1X Phosphate Buffered Saline (PBS): To prepare 1L 1X PBS: add 100 ml 10X PBS (#12528) to 900 ml water, mix.
  2. 4% Formaldehyde, Methanol-Free: (#47746): Use fresh.
  3. Blocking Buffer: Purchase ready-to-use Immunofluorescence Blocking Buffer (#12411), or prepare a 1X PBS / 5% normal serum / 0.3% Triton X-100 buffer by adding 0.5 ml normal serum (e.g., Normal Goat Serum (#5425)) and 30 µL Triton X-100 to 9.5 ml 1X PBS. Mix well and store at 4°C.
  4. Antibody Dilution Buffer: (1X PBS / 0.3% Triton X-100): To prepare 10 ml, add 30 µl Triton X-100 to 10 ml 1X PBS. Mix well.
  5. Mounting medium: Prolong® Gold AntiFade Reagent (#9071) or Prolong® Gold AntiFade Reagent with DAPI (#8961).

B. Specimen Preparation - Frozen/Cryostat Sections

  1. For fixed frozen tissue proceed with Section C.
  2. For fresh, unfixed frozen tissue, fix specimens using the follow procedure:
    1. Cover sections with 4% formaldehyde for 15 minutes at room temperature.
    2. Aspirate fixative, wash three times in 1X PBS for 5 minutes each.

C. Procedure

NOTE: Do not allow specimens to dry at any time during this procedure and protect sensitive fluorophores from light.

  1. Block specimen in Blocking Buffer for 60 minutes.
  2. While blocking, prepare primary antibody in Antibody Dilution Buffer (see product website for recommended dilution range).
  3. Aspirate blocking solution, apply diluted primary antibody.
  4. Incubate overnight at 4°C.
  5. Wash three times with 1X PBS for 5 minutes each.
  6. Counterstain as appropriate and then mount samples for imaging.
  7. For long term storage, store stained samples at 4°C protected from light.

Protocol Id: 3269

Immunofluorescence (Immunocytochemistry), BSA-free Protocol for Directly Conjugated Antibodies

A. Solutions and Reagents

NOTE: Prepare solutions with reverse osmosis deionized (RODI) or equivalently purified water.

  1. 1X Phosphate Buffered Saline (PBS): To prepare 1 L 1X PBS: add 100 ml 10X PBS (#12528) to 900 ml water, mix.
  2. 4% Formaldehyde, Methanol-Free: (#47746): Use fresh.
  3. Blocking Buffer: Purchase ready-to-use Immunofluorescence Blocking Buffer (#12411), or prepare a 1X PBS / 5% normal serum / 0.3% Triton X-100 buffer by adding 0.5 mL normal serum (e.g., Normal Goat Serum (#5425)) and 30 µL Triton X-100 to 9.5 mL 1X PBS. Mix well and store at 4°C.
  4. Antibody Dilution Buffer (1X PBS / 0.3% Triton X-100): To prepare 10 ml, add 30 µl Triton X-100 to 10 ml 1X PBS. Mix well.
  5. Mounting medium: Prolong® Gold AntiFade Reagent (#9071) or Prolong® Gold AntiFade Reagent with DAPI (#8961).

B. Procedure

NOTE: Do not allow cells to dry at any time during this procedure and protect sensitive fluorophores from light.

  1. Fix cells with 4% formaldehyde for 15 minutes at room temperature.
  2. Aspirate fixative, wash three times with 1X PBS for 5 minutes each.
  3. Block specimen in Blocking Buffer for 60 minutes.
  4. While blocking, prepare primary antibody in Antibody Dilution Buffer (see product website for recommended dilution range).
  5. Aspirate blocking solution, apply diluted primary antibody.
  6. Incubate overnight at 4°C.
  7. Wash three times with 1X PBS for 5 minutes each.
  8. Counterstain as appropriate and then mount samples for imaging.
  9. For long term storage, store stained samples at 4°C protected from light.

Protocol Id: 3192

Specificity / Sensitivity

Keratin 5 (E2T4B) XP® Rabbit mAb (Alexa Fluor® 488 Conjugate) recognizes endogenous levels of total keratin 5 protein.

Species Reactivity:

Human, Mouse

Source / Purification

Monoclonal antibody is produced by immunizing animals with a synthetic peptide corresponding to residues surrounding Val578 of human keratin 5 protein.

Background

Keratins (cytokeratins) are intermediate filament proteins that are mainly expressed in epithelial cells. Keratin heterodimers composed of an acidic keratin (or type I keratin, keratins K9-K28) and a basic keratin (or type II keratin, keratins K1-K8 and K71-K80) assemble to form filaments. Keratin isoforms demonstrate tissue- and differentiation-specific profiles that make them useful as research and clinical biomarkers (1,2).

Dysregulation/mutations in keratin genes can lead to a variety of disorders affecting the skin, hair, nails, and other epithelial tissues (3). While expression of keratins can be variable, immunohistochemical staining of keratins is widely used to help in the identification and classification of epithelial tumors, and may also provide prognostic information.

Keratins 8 and 18 (K8/K18) are expressed in simple epithelia of normal tissue, as well as in adenocarcinomas of the breast, lung, ovary, and gastrointestinal tract. Keratin 17 is expressed in basal keratinocytes of stratified epithelia, hair follicles, and sebaceous glands. Onset of keratin 17 expression coincides with the definition of major epithelial lineages during skin development (4). Keratin 14 (K14) is expressed in basal cells of stratified epithelia, and in basal-like subtypes of breast cancer and squamous cell carcinomas. Keratin 19 (K19) is expressed in glandular epithelia, including the liver, gallbladder, and pancreas, as well as in adenocarcinomas of the breast, thyroid, and bile duct. Keratin 20 (K20) is expressed in gastrointestinal epithelium, urothelium, and Merkel cells in the skin, as well as in colorectal carcinomas and some urothelial carcinomas. Keratin 5/6 (K5/6) is expressed in basal cells of stratified epithelia, including the skin, prostate, and breast, as well as in basal-like breast cancers, squamous cell carcinomas, and some lung carcinomas. Keratin 7 (K7) is expressed in glandular epithelia, such as those in the lung, breast, and female reproductive tract, as well as in adenocarcinomas of the lung, breast, and ovary (5,6).

Keratins, particularly K8, K18, and K19, serve as biomarkers for identification of circulating tumor cells (CTCs) (5).

Post-translational modifications, including phosphorylation, acetylation, ubiquitylation, sumoylation, glycosylation, and transamidation, have been shown to affect the functions of keratins in normal and disease states (6). Understanding the molecular mechanisms underlying these PTMs may provide insights into cancer pathogenesis.

Limited Uses

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For Research Use Only. Not for Use in Diagnostic Procedures.
Cell Signaling Technology is a trademark of Cell Signaling Technology, Inc.
Alexa Fluor is a registered trademark of Life Technologies Corporation.
XP is a registered trademark of Cell Signaling Technology, Inc.
This product is provided under an intellectual property license from Life Technologies Corporation. The transfer of this product is conditioned on the buyer using the purchased product solely in research conducted by the buyer, excluding contract research or any fee for service research, and the buyer must not (1) use this product or its components for (a) diagnostic, therapeutic or prophylactic purposes; (b) testing, analysis or screening services, or information in return for compensation on a per-test basis; or (c) manufacturing or quality assurance or quality control, and/or (2) sell or transfer this product or its components for resale, whether or not resold for use in research. For information on purchasing a license to this product for purposes other than as described above, contact Life Technologies Corporation, 5791 Van Allen Way, Carlsbad, CA 92008 USA or [email protected].
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