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Tonsil showing many TIGIT positive lymphocytes are in the interfollicular area while the strongest TIGIT staining occurs in a subset of lymphocytes in the germinal centre

Staining Pattern in Normal Tissues

Manual protocol

Freshly cut sections should be used (less than 10 days between cutting and staining). Heat-induced antigen retrieval for 5 minutes in an autoclave at 121°C in pH 7,8 Target Retrieval Solution buffer. Apply HMV322 at a dilution of 1:150 at 37°C for 60 minutes. Visualization of bound antibody by the EnVision Kit (Dako, Agilent) according to the manufacturer’s directions.

BrainCerebrum, grey Negative
Cerebrum, white Negative
Cerebellum, cortex Negative
Cerebellum, white Weak to moderate, nuclear staining of a subset of (probaly glial) cells (crossreactivity).
Ganglion Negative
Ependyma Negative
Eye, retina Negative
Endocrine TissuesThyroid Negative
Parathyroid gland Negative
Adrenal gland Negative
Pituitary gland, anterior lobe Negative
Pituitary gland, posterior lobe Negative
Respiratory systemLung bronchi Negative
Lung, bronchial glands Negative
Nose, paranasal sinus Negative
Lung, parenchyma Negative
Proximal digestive tractLip Negative
Oral cavity Negative
Tonsil, surface Negative
Esophagus, mucosa Negative
Lip, small salivary gland Negative
Sublingual gland Negative
Parotid gland Negative
Submandibullary gland Negative
Gastronintestinal tractStomach, antrum Negative
Stomach, fundus and corpus Negative
Small intestine, duodenum Negative
Duodenum, Brunner gland Negative
Small intestine, ileum Negative
Appendix Negative
Colon descendens Negative
Rectum Negative
Anal canal, transition epithelium Negative
Liver, Gallbladder, PancreasLiver Negative
Gallbladder Negative
Pancreas Negative
Kidney, urinary bladderKidney, cortex Negative
Kidney, medulla Negative
Urinary bladder, urothelium Negative
Kidney pelvis, mucosa Negative
Male tissuesProstate Negative
Seminal vesicle Negative
Epididymis caput Negative
Epididymis cauda Negative
Testis Negative
Female TissuesBreast, glands Negative
Ectocervix Negative
Endocervix Negative
Endometrium, proliferation Negative
Endometrium, secretion Negative
Uterus, myometrium Negative
Fallopian tube Negative
Ovary, stroma Negative
Ovary, follicular cyst Negative
Ovary, corpus luteum Negative
Amnion Negative
Chorion Negative
Amnion/Chorion Negative
Placenta, early, decidua Negative
Placenta, first trimenon Negative
Placenta, mature Negative
Muscle, connective & soft tissueAorta, intima Negative
Skeletal muscle Negative
Aorta, media Negative
Skeletal muscle, tongue Negative
Heart, left ventricle Negative
Kidney pelvis, muscular wall Negative
Urinary bladder, muscular wall Negative
Esophagus, muscular wall Negative
Stomach, muscular wall Negative
Ileum, muscular wall Negative
Appendix, muscular wall Negative
Colon descendens, muscular wall Negative
Penis, glans, corpus spongiosum Negative
Fat, white Negative
SkinSkin, surface Negative
Skin (hairs, sebaceous glands) Negative
Anal canal, skin Negative
Scrotum Negative
Bone Marrow & lymphoid tissuesBone marrow Negative
Thymus Weak to moderate TIGIT staining of a subset of lymphocytes.
Spleen Weak to moderate TIGIT staining of a subset of lymphocytes.
Lymph node Most TIGIT positive lymphocytes are in the interfollicular area while the strongest TIGIT staining occurs in the few labeled lymphocytes in germinal centres.
Tonsil, deep Variable levels of TIGIT staining in subsets of follicular and interfollicular lymphocytes. The highest level of expression occurs in CD4+ follicular T helper cells located in the germinal centre periphery orientated towards the tonsil surface epithelium.

TIGIT

(HMV322)

TIGIT is a pivotal target in immune-oncology.

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TIGIT (HMV322)
€295.00

Details

Type
Recombinant Rabbit monoclonal / IgG
Clone
HMV322
Reactivity
Human

More product details

Biology behind

TIGIT (T cell immunoreceptor with Ig and ITIM domains) is a transmembrane glycoprotein of the poliovirus receptor (PVR) family which is coded by the TIGIT gene at 3q13.31. TIGIT acts as an inhibitory immune receptor (immune checkpoint) which can bind to CD155 with high affinity, and to CD112 with lower affinity. TIGIT expression is restricted to some CD8+ cytotoxic T cells, CD4+ T helper cells, FOXP3+ regulatory T cells, and NK cells. The highest level of expression occurs in CD4+ follicular T helper cells located in the germinal centre periphery orientated towards the tonsil surface epithelium. TIGIT expression has a limiting effect on antitumoral immune reactions. TIGIT inhibition, by either genetic ablation or blocking antibodies, increases T-cell activation and proliferation in response to stimulation and consequently results in reduced tumor growth in experimental models. Various compounds targeting TIGIT have been developed (i.e. tiragolumab, domvanalimab, vibostolimab, etigilimab, m6223, ociperlimab) and are currently evaluated in clinical trials, mostly in combination with other immune checkpoint inhibitors.

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Potential Research Applications

Evidence For Antibody Specificity In I H C