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SAB5500124

Anti-Keratin 14 antibody, Rabbit monoclonal

clone SP53, recombinant, expressed in proprietary host, affinity isolated antibody

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100 μL

$393.00

$393.00


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About This Item

NACRES:
NA.41
UNSPSC Code:
12352203
Conjugate:
unconjugated
Clone:
SP53, monoclonal
Application:
FACS, IHC
Citations:
4

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biological source

rabbit

recombinant

expressed in proprietary host

conjugate

unconjugated

antibody form

affinity isolated antibody

antibody product type

primary antibodies

clone

SP53, monoclonal

species reactivity

human (tested)

species reactivity (predicted by homology)

rat, bovine, mouse, pig

technique(s)

flow cytometry: 1:100, immunoblotting: 1:25, immunohistochemistry: 1:100

isotype

IgG

UniProt accession no.

shipped in

wet ice

storage temp.

2-8°C

target post-translational modification

unmodified

Quality Level

Gene Information

human ... KRT14(3861)

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This Item
SAB4501657C8791SAB5500066
species reactivity

human (tested)

species reactivity

mouse, human, rat

species reactivity

human

species reactivity

human (tested)

biological source

rabbit

biological source

rabbit

biological source

mouse

biological source

rabbit

clone

SP53, monoclonal

clone

polyclonal

clone

CKB1, monoclonal

clone

SP219, monoclonal

antibody form

affinity isolated antibody

antibody form

affinity isolated antibody

antibody form

ascites fluid

antibody form

affinity isolated antibody

conjugate

unconjugated

conjugate

unconjugated

conjugate

unconjugated

conjugate

unconjugated

Gene Information

human ... KRT14(3861)

Gene Information

human ... KRT14(3861)

Gene Information

human ... KRT14(3861)

Gene Information

human ... GP1BA(2811)

General description

Keratin 14 belongs to the type A (acidic) subfamily of low molecular weight keratins and exists in combination with keratin 5.

Immunogen

Synthetic peptide corresponding to C-terminus of human cytokeratin 14.

Features and Benefits

Evaluate our antibodies with complete peace of mind. If the antibody does not perform in your application, we will issue a full credit or replacement antibody. Learn more.

Physical form

0.1 ml rabbit monoclonal antibody purified by protein A/G in PBS/1% BSA buffer pH 7.6 with less than 0.1% sodium azide.

Disclaimer

Unless otherwise stated in our catalog or other company documentation accompanying the product(s), our products are intended for research use only and are not to be used for any other purpose, which includes but is not limited to, unauthorized commercial uses, in vitro diagnostic uses, ex vivo or in vivo therapeutic uses or any type of consumption or application to humans or animals.

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Storage Class

10 - Combustible liquids

wgk

WGK 2

flash_point_f

Not applicable

flash_point_c

Not applicable


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Atieh Abedin-Do et al.
Frontiers in bioengineering and biotechnology, 10, 989888-989888 (2022-10-18)
The prevalence of diabetes is increasing worldwide. Diabetes contributes to 70% of all non-traumatic lower-limb amputations, which are directly caused by diabetic foot ulcers (DFU) that are difficult to heal. Non-healing diabetic ulcers represent one of modern society's most difficult
Vanessa Delcroix et al.
Cells, 12(10) (2023-07-06)
The lacrimal gland (LG) secretes aqueous tears. Previous studies have provided insights into the cell lineage relationships during tissue morphogenesis. However, little is known about the cell types composing the adult LG and their progenitors. Using scRNAseq, we established the
Matthew P Dent et al.
Toxicology in vitro : an international journal published in association with BIBRA, 60, 203-211 (2019-06-04)
The development and normal function of prostate tissue depends on signalling interactions between stromal and epithelial compartments. Development of a prostate microtissue composed of these two components can help identify substance exposures that could cause adverse effects in humans as
Matthew P Dent et al.
Environment international, 83, 94-106 (2015-06-27)
Toxicology testing is undergoing a transformation from a system based on high-dose studies in laboratory animals to one founded primarily on in vitro methods that evaluate changes in normal cellular signalling pathways using human-relevant cells or tissues. We review the

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