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AB315276

Anti-LAMA1 antibody [EPR27259-172] - BSA and Azide free

  • BOND RX™ Validated
  • RabMAb
  • Recombinant
  • KO Validated
  • Advanced Validation
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Knockout Tested Rabbit Recombinant Monoclonal LAMA1 antibody. Carrier free. Suitable for mIHC, IHC-P, WB, Dot and reacts with Human, Mouse, Rat, Recombinant full length protein - Human samples.

View Alternative Names

LAMA, LAMA1, Laminin subunit alpha-1, Laminin A chain, Laminin-1 subunit alpha, Laminin-3 subunit alpha, S-laminin subunit alpha, S-LAM alpha

12 Images
Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections) - Anti-LAMA1 antibody [EPR27259-172] - BSA and Azide free (AB315276)
  • IHC-P

Supplier Data

Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections) - Anti-LAMA1 antibody [EPR27259-172] - BSA and Azide free (AB315276)

This data was developed using ab315275, the same antibody clone in a different buffer formulation.

Immunohistochemical analysis of paraffin-embedded Human kidney tissue labeling LAMA1 with ab315275 at 1/500 (1.018 ug/ml) dilution, followed by a ready to use LeicaDS9800 (Bond™ Polymer Refine Detection).

Positive staining on basement membrane of human kidney. The section was incubated with ab315275 for 30 mins at room temperature. The immunostaining was performed on a Leica Biosystems BOND® RX instrument. Counterstained with Hematoxylin.

Secondary antibody only control : Secondary antibody is a ready to use LeicaDS9800 (Bond™ Polymer Refine Detection).

Heat mediated antigen retrieval was performed with Tris-EDTA buffer (pH 9.0, Epitope Retrieval Solution2) for 20 mins.

Multiplex immunohistochemistry - Anti-LAMA1 antibody [EPR27259-172] - BSA and Azide free (AB315276)
  • mIHC

Lab

Multiplex immunohistochemistry - Anti-LAMA1 antibody [EPR27259-172] - BSA and Azide free (AB315276)

This data was developed using ab315275, the same antibody clone in a different buffer formulation.

Panel A : anti-Oligodendrocyte Specific Protein (green; Opal™520), anti-LAMA1 (magenta; Opal™690) and anti-DDX/MVH (gray; Opal™570) on human testis. Panel B : anti-Oligodendrocyte Specific Protein staining apical Sertoli cell crypts in human testis. Panel C : anti-LAMA1 staining basement membrane in human testis. Panel D : anti-DDX4/MVH staining spermatogonia in human testis. Nuclear DNA was labeled with DAPI (shown in blue). The section was incubated in three rounds of staining : in the order of ab323317, ab315275 and ab270534 for 30 mins at room temperature. Each round was followed by a separate fluorescent tyramide signal amplification system. The immunostaining was performed on a Leica Biosystems BOND® RX instrument with an Opal™ 4-color kit. Image acquisition was performed with Leica SP8 confocal microscope.

Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections) - Anti-LAMA1 antibody [EPR27259-172] - BSA and Azide free (AB315276)
  • IHC-P

Supplier Data

Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections) - Anti-LAMA1 antibody [EPR27259-172] - BSA and Azide free (AB315276)

This data was developed using ab315275, the same antibody clone in a different buffer formulation.

Immunohistochemical analysis of paraffin-embedded Human testis tissue labeling LAMA1 with ab315275 at 1/500 (1.018 ug/ml) dilution, followed by a ready to use LeicaDS9800 (Bond™ Polymer Refine Detection).

Positive staining on basement membrane of human testis. The section was incubated with ab315275 for 30 mins at room temperature. The immunostaining was performed on a Leica Biosystems BOND® RX instrument. Counterstained with Hematoxylin.

Secondary antibody only control : Secondary antibody is a ready to use LeicaDS9800 (Bond™ Polymer Refine Detection).

Heat mediated antigen retrieval was performed with Tris-EDTA buffer (pH 9.0, Epitope Retrieval Solution2) for 20 mins.

Multiplex immunohistochemistry - Anti-LAMA1 antibody [EPR27259-172] - BSA and Azide free (AB315276)
  • mIHC

Lab

Multiplex immunohistochemistry - Anti-LAMA1 antibody [EPR27259-172] - BSA and Azide free (AB315276)

This data was developed using ab315275, the same antibody clone in a different buffer formulation.

Multiplex immunohistochemistry analysis of formalin/PFA-fixed paraffin-embedded human testis tissue staining CYP51A1/CYP51 with ab315800 at a 1/2000 dilution, ab270534 anti-DDX4 / MVH used at 1/2000 dilution and ab315275 anti-LAMA1 used at a 1/500 dilution. Opal Polymer HRP Ms + Rb was used as a secondary antibody.

Panel A : merged staining of anti-CYP51A1/CYP51 (green; Opal520), anti-DDX4 / MVH (magenta; Opal690) and anti-LAMA1 (grey; Opal570) on human testis. Panel B : anti-CYP51A1/CYP51 staining leydig cells in human testis.
Panel C : anti-DDX4 / MVH staining spermatogonia and spermatocytes in human testis.
Panel D : anti-LAMA1 staining basement membrane in human testis.
Nuclear DNA was labeled with DAPI (shown in blue).

The section was incubated in three rounds of staining : in the order of ab315800, ab270834 and ab315275 for 30 mins at room temperature. Each round was followed by a separate fluorescent tyramide signal amplification system.

The immunostaining was performed on a Leica Biosystems BOND®RX instrument with an Opal 4-color kit. Image acquisition was performed with Leica SP8 confocal microscope.

Heat mediated antigen retrieval with Tris-EDTA buffer (pH 9.0, epitope retrieval solution2) for 20 mins.

Multiplex immunohistochemistry - Anti-LAMA1 antibody [EPR27259-172] - BSA and Azide free (AB315276)
  • mIHC

Lab

Multiplex immunohistochemistry - Anti-LAMA1 antibody [EPR27259-172] - BSA and Azide free (AB315276)

This data was developed using ab315275, the same antibody clone in a different buffer formulation.

Multiplex immunohistochemistry analysis of formalin/PFA-fixed paraffin-embedded mouse testis tissue staining CYP51A1/CYP51 with ab315800 at a 1/2000 dilution, ab270534 anti-DDX4 / MVH used at 1/2000 dilution and ab315275 anti-LAMA1 used at a 1/500 dilution. Opal Polymer HRP Ms + Rb was used as a secondary antibody.

Panel A : merged staining of anti-CYP51A1/CYP51 (green; Opal520), anti-DDX4 / MVH (magenta; Opal690) and anti-LAMA1 (grey; Opal570) on mouse testis. Panel B : anti-CYP51A1/CYP51 staining leydig cells in mouse testis.
Panel C : anti-DDX4 / MVH staining spermatogonia and spermatocytes in mouse testis.
Panel D : anti-LAMA1 staining basement membrane in mouse testis.
Nuclear DNA was labeled with DAPI (shown in blue).

The section was incubated in three rounds of staining : in the order of ab315800, ab270834 and ab315275 for 30 mins at room temperature. Each round was followed by a separate fluorescent tyramide signal amplification system.

The immunostaining was performed on a Leica Biosystems BOND®RX instrument with an Opal 4-color kit. Image acquisition was performed with Leica SP8 confocal microscope.

Heat mediated antigen retrieval with Tris-EDTA buffer (pH 9.0, epitope retrieval solution2) for 20 mins.

Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections) - Anti-LAMA1 antibody [EPR27259-172] - BSA and Azide free (AB315276)
  • IHC-P

Supplier Data

Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections) - Anti-LAMA1 antibody [EPR27259-172] - BSA and Azide free (AB315276)

This data was developed using ab315275, the same antibody clone in a different buffer formulation.

Immunohistochemical analysis of paraffin-embedded Rat testis tissue labeling LAMA1 with ab315275 at 1/500 (1.018 ug/ml) dilution, followed by a ready to use LeicaDS9800 (Bond™ Polymer Refine Detection).

Positive staining on basement membrane of rat testis. The section was incubated with ab315275 for 30 mins at room temperature. The immunostaining was performed on a Leica Biosystems BOND® RX instrument. Counterstained with Hematoxylin.

Secondary antibody only control : Secondary antibody is a ready to use LeicaDS9800 (Bond™ Polymer Refine Detection).

Heat mediated antigen retrieval was performed with Tris-EDTA buffer (pH 9.0, Epitope Retrieval Solution2) for 20 mins.

Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections) - Anti-LAMA1 antibody [EPR27259-172] - BSA and Azide free (AB315276)
  • IHC-P

Supplier Data

Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections) - Anti-LAMA1 antibody [EPR27259-172] - BSA and Azide free (AB315276)

This data was developed using ab315275, the same antibody clone in a different buffer formulation.

Immunohistochemical analysis of paraffin-embedded Mouse testis tissue labeling LAMA1 with ab315275 at 1/500 (1.018 ug/ml) dilution, followed by a ready to use LeicaDS9800 (Bond™ Polymer Refine Detection).

Positive staining on basement membrane of mouse testis. The section was incubated with ab315275 for 30 mins at room temperature. The immunostaining was performed on a Leica Biosystems BOND® RX instrument. Counterstained with Hematoxylin.

Secondary antibody only control : Secondary antibody is a ready to use LeicaDS9800 (Bond™ Polymer Refine Detection).

Heat mediated antigen retrieval was performed with Tris-EDTA buffer (pH 9.0, Epitope Retrieval Solution2) for 20 mins.

Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections) - Anti-LAMA1 antibody [EPR27259-172] - BSA and Azide free (AB315276)
  • IHC-P

Supplier Data

Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections) - Anti-LAMA1 antibody [EPR27259-172] - BSA and Azide free (AB315276)

This data was developed using ab315275, the same antibody clone in a different buffer formulation.

Immunohistochemical analysis of paraffin-embedded Rat kidney tissue labeling LAMA1 with ab315275 at 1/500 (1.018 ug/ml) dilution, followed by a ready to use LeicaDS9800 (Bond™ Polymer Refine Detection).

Positive staining on basement membrane of rat kidney. The section was incubated with ab315275 for 30 mins at room temperature. The immunostaining was performed on a Leica Biosystems BOND® RX instrument. Counterstained with Hematoxylin.

Secondary antibody only control : Secondary antibody is a ready to use LeicaDS9800 (Bond™ Polymer Refine Detection).

Heat mediated antigen retrieval was performed with Tris-EDTA buffer (pH 9.0, Epitope Retrieval Solution2) for 20 mins.

Multiplex immunohistochemistry - Anti-LAMA1 antibody [EPR27259-172] - BSA and Azide free (AB315276)
  • mIHC

Lab

Multiplex immunohistochemistry - Anti-LAMA1 antibody [EPR27259-172] - BSA and Azide free (AB315276)

This data was developed using ab315275, the same antibody clone in a different buffer formulation.

Multiplex immunohistochemistry analysis of formalin/PFA-fixed paraffin-embedded rat testis tissue staining CYP51A1/CYP51 with ab315800 at a 1/2000 dilution, ab270534 anti-DDX4 / MVH used at 1/2000 dilution and ab315275 anti-LAMA1 used at a 1/500 dilution. Opal Polymer HRP Ms + Rb was used as a secondary antibody.

Panel A : merged staining of anti-CYP51A1/CYP51 (green; Opal520), anti-DDX4 / MVH (magenta; Opal690) and anti-LAMA1 (grey; Opal570) on rat testis. Panel B : anti-CYP51A1/CYP51 staining leydig cells in rat testis.
Panel C : anti-DDX4 / MVH staining spermatogonia and spermatocytes in rat testis.
Panel D : anti-LAMA1 staining basement membrane in rat testis.
Nuclear DNA was labeled with DAPI (shown in blue).

The section was incubated in three rounds of staining : in the order of ab315800, ab270834 and ab315275 for 30 mins at room temperature. Each round was followed by a separate fluorescent tyramide signal amplification system.

The immunostaining was performed on a Leica Biosystems BOND®RX instrument with an Opal 4-color kit. Image acquisition was performed with Leica SP8 confocal microscope.

Heat mediated antigen retrieval with Tris-EDTA buffer (pH 9.0, epitope retrieval solution2) for 20 mins.

Western blot - Anti-LAMA1 antibody [EPR27259-172] - BSA and Azide free (AB315276)
  • WB

Supplier Data

Western blot - Anti-LAMA1 antibody [EPR27259-172] - BSA and Azide free (AB315276)

This data was developed using ab315275, the same antibody clone in a different buffer formulation.

Blocking and diluting buffer and concentration : 5% NFDM/TBST.

Negative control : HDLM-2

In Western blot, Anti-Vinculin antibody [EPR8185] (ab129002) staining at 1/10000 dilution.

All lanes:

Western blot - Anti-LAMA1 antibody [EPR27259-172] (<a href='/en-us/products/primary-antibodies/lama1-antibody-epr27259-172-ab315275'>ab315275</a>) at 1/1000 dilution

Lane 1:

SK-MEL-2 (human skin malignant melanoma cell) whole cell lysate at 20 µg

Lane 2:

HeLa (human cervical adenocarcinoma epithelial cell) whole cell lysate at 20 µg

Lane 3:

HDLM-2 (human Hodgkin lymphoma) whole cell lysate at 20 µg

Secondary

All lanes:

Western blot - Goat Anti-Rabbit IgG H&L (HRP) (<a href='/en-us/products/secondary-antibodies/goat-rabbit-igg-h-l-hrp-ab97051'>ab97051</a>) at 1/100000 dilution

Observed band size: 337 kDa,124 kDa

false

Exposure time: 180s

Western blot - Anti-LAMA1 antibody [EPR27259-172] - BSA and Azide free (AB315276)
  • WB

Supplier Data

Western blot - Anti-LAMA1 antibody [EPR27259-172] - BSA and Azide free (AB315276)

This data was developed using ab315275, the same antibody clone in a different buffer formulation.

Blocking and diluting buffer and concentration : 5% NFDM/TBST.

Negative control : A431

In Western blot, ab315275 was shown to bind specifically to LAMA1. A band was observed at 337 kDa in wild-type HeLa cell lysates whereas no signal observed at this size in LAMA1 knockout cell line ab264991 (KO cell lysate ab258937).

In Western blot, Anti-Vinculin antibody [EPR8185] (ab129002) staining at 1/10000 dilution.

All lanes:

Western blot - Anti-LAMA1 antibody [EPR27259-172] (<a href='/en-us/products/primary-antibodies/lama1-antibody-epr27259-172-ab315275'>ab315275</a>) at 1/1000 dilution

Lane 1:

Wild-type HeLa (human cervical adenocarcinoma epithelial cell) whole cell lysate at 20 µg

Lane 2:

LAMA1 knockout HeLa whole cell lysate at 20 µg

Lane 3:

U-2 OS (human bone osteosarcoma epithelial cell) whole cell lysate at 20 µg

Lane 4:

A431 (human epidermoid carcinoma epithelial cell) whole cell lysate at 20 µg

Secondary

All lanes:

Western blot - Goat Anti-Rabbit IgG H&L (HRP) (<a href='/en-us/products/secondary-antibodies/goat-rabbit-igg-h-l-hrp-ab97051'>ab97051</a>) at 1/100000 dilution

Observed band size: 337 kDa,124 kDa

false

Exposure time: 81s

Dot Blot - Anti-LAMA1 antibody [EPR27259-172] - BSA and Azide free (AB315276)
  • Dot

Supplier Data

Dot Blot - Anti-LAMA1 antibody [EPR27259-172] - BSA and Azide free (AB315276)

This data was developed using ab315275, the same antibody clone in a different buffer formulation.

Dot blot analysis of LAMA1 using ab315275 at 1 : 1000 (0.509 ug/ml) followed by a Goat Anti-Rabbit IgG, (H+L), Peroxidase conjugated (ab97051) at 1 : 100,000 dilution.

Exposure time : 180s.

Blocking and diluting buffer and concentration : 5% NFDM/TBST.

Key facts

Host species

Rabbit

Clonality

Monoclonal

Clone number

EPR27259-172

Isotype

IgG

Carrier free

Yes

Reacts with

Human, Mouse, Rat

Applications

mIHC, IHC-P, WB, Dot

applications

Immunogen

The exact immunogen used to generate this antibody is proprietary information.

Specificity

Unsuitable for Ms WB and Rt WB.

Reactivity data

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Product details

ab315276 is the carrier-free version of ab315275.

Patented technology
Our RabMAb® technology is a patented hybridoma-based technology for making rabbit monoclonal antibodies. For details on our patents, please refer to RabMAb® patents.

What are the advantages of a recombinant monoclonal antibody?
This product is a recombinant monoclonal antibody, which offers several advantages including:

  • - High batch-to-batch consistency and reproducibility
  • - Improved sensitivity and specificity
  • - Long-term security of supply
  • - Animal-free batch production

For more information, read more on recombinant antibodies.

Conjugation ready
Our carrier-free antibodies are typically supplied in a PBS-only formulation, purified and free of BSA, sodium azide and glycerol. This conjugation-ready format is designed for use with fluorochromes, metal isotopes, oligonucleotides, and enzymes, which makes them ideal for antibody labelling, functional and cell-based assays, flow-based assays (e.g. mass cytometry) and Multiplex Imaging applications.

Use our conjugation kits for antibody conjugates that are ready-to-use in as little as 20 minutes with 1 minute hands-on-time and 100% antibody recovery: available for fluorescent dyes, HRP, biotin and gold.

Compatibility
This product is compatible with the Maxpar® Antibody Labeling Kit from Fluidigm, without the need for antibody preparation. Maxpar® is a trademark of Fluidigm Canada Inc.

Properties and storage information

Form
Liquid
Purification technique
Affinity purification Protein A
Storage buffer
pH: 7.2 - 7.4 Constituents: PBS
Shipped at conditions
Blue Ice
Appropriate short-term storage conditions
+4°C
Appropriate long-term storage conditions
+4°C

Supplementary information

This supplementary information is collated from multiple sources and compiled automatically.

LAMA1 also known as laminin subunit alpha-1 is a component of the extracellular matrix with a molecular mass of approximately 400 kDa. It is part of the laminin family a group of glycoproteins that play key roles in maintaining structural integrity and signaling in tissues. LAMA1 is widely expressed in basement membranes of many tissues particularly in the brain kidney and other organs with complex architecture. Researchers often explore its expression patterns using techniques like laminin histology and laminin microscope analysis.
Biological function summary

This protein acts as a structural scaffold and cell adhesion mediator. LAMA1 integrates into the laminin-1 trimer complex composed of alpha beta and gamma chains supporting cellular attachment differentiation and migration. This assembly aids in tissue morphogenesis and repair processes. It creates an important interface between cells and the extracellular matrix influencing cellular behavior and maintaining tissue function.

Pathways

LAMA1 interacts with cellular signaling cascades such as the PI3K/AKT pathway and the TGF-beta pathway. These pathways play significant roles in cellular growth survival and differentiation. LAMA1's interaction with other proteins like integrins and heparan sulfate proteoglycans facilitates its role in these pathways impacting diverse processes like embryonic development and tissue remodeling.

LAMA1 shows a connection to conditions such as Pierson syndrome and certain congenital muscular dystrophies. Mutations in LAMA1 can lead to basement membrane defects contributing to these diseases' pathological features. Additionally interactions with proteins like collagen IV and perlecan are significant as these complexes can further influence disease severity and progression. Understanding LAMA1's role provides insights into potential therapeutic approaches for related disorders.

Product protocols

For this product, it's our understanding that no specific protocols are required. You can visit:

Target data

Binding to cells via a high affinity receptor, laminin is thought to mediate the attachment, migration and organization of cells into tissues during embryonic development by interacting with other extracellular matrix components. As a ligand for alpha-dystroglycan, it is involved in a number of processes including epithelium branching morphogenesis, down-regulation of apoptotic signals in muscle via the activation of PI3K/AKT signaling, and activation of RAC1 signaling. As a subunit of laminin-1 (also known as laminin-111 or EHS laminin), it is involved in the stimulation of agrin-induced receptor clustering through a MuSK-independent pathway.
See full target information LAMA1

Product promise

We are committed to supporting your work with high-quality reagents, and we're here for you every step of the way. In the unlikely event that one of our products does not perform as expected, you're protected by our Product Promise.
For full details, please see our Terms & Conditions

Please note: All products are 'FOR RESEARCH USE ONLY. NOT FOR USE IN DIAGNOSTIC OR THERAPEUTIC PROCEDURES'.

For licensing inquiries, please contact partnerships@abcam.com